Difference between revisions of "Team:UC Davis/Design"

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     <div style = 'padding-top:100px;padding-bottom: 60px; font-size: 30px; color: #d9a900'; ><b>Project Design </b></div>
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     <a href="#Introduction">Introduction</a>
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     <a href="#Scientific Overview">Scientific Overview</a>
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    <a href="#Environmental Overview">Environmental Overview</a>
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    <a href="#Cultural Context">Cultural Context</a>
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    <a href="#Political/Legislative Context">Political/Legislative Context</a>
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    <a href="#How We Proceeded">How We Proceeded</a>
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    <a href="#Evaluations">Evaluations</a>
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    <a href="#Lessons Learned">Lessons Learned</a>
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    <a href="#Works Cited">Works Cited</a>
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    <a href="#Appendix">Appendix</a>
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  <div style = 'padding-top:100px;padding-bottom: 60px; font-size: 30px; color: #d9a900'; ><b>Integrating Human Practices</b></div>
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<div id="Introduction" style = 'font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
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            Introduction
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          </b></i>
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     </div>
  
     <div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Bioassay Design</b></div>
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      We designed a mammalian cell-based bioassay that reports activation of specific stress pathways via fluorescence, for use in environmental toxicology. To do this, we selected transcriptionally regulated target genes which are present in mammalian cells and are involved in stress pathways. We isolated the promoters with transcription factor binding sites from these target genes and coupled them to a fluorescent reporter gene. We selected EGFP, a variant of green fluorescent protein (GFP). GFP is ubiquitous in synthetic biology due to its reliability and ease of measurement [1]. EGFP is derived from GFP, and has been optimized for use in mammalian systems. When a chemical of concern is screened using our assay, if it triggers a specific stress response, the reporter gene will be expressed, causing the assay to fluoresce. The fluorescence of the assay can be quantitatively measured and analyzed. This assay will provide data on the effect of chemicals of concern on the physiological health of mammalian cells; measurements may be easily taken a range of concentrations, durations of exposure, salinities, pH, temperatures, nutrient availabilities, and other conditions. This also allows for measurement of synergistic or interfering effects due to multiple chemicals of concern present simultaneously.
+
  
<p>We selected 8 promoter constructs derived from 5 target genes (see Figure 1 below) and coupled them to EGFP. This promoter and reporter gene construct was inserted into a plasmid and transfected into two cell lines (see Figure 2 below). The resulting bioassays were exposed to different chemicals of concern at a variety of concentrations and conditions (see Figure 3 below).
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      A guiding theme which we returned to again and again, as we designed our project, was the awareness that science does not happen in a vacuum. Science and technology exist within social frameworks– public policy, economics, public opinion, and overall acceptance of a new innovation are crucial factors to consider. A well researched, well tested product can and will fail the essential test of ‘usefulness’ if external social factors are disregarded. A product that the public will not accept and use is a poorly designed product. This is especially true within the field of synthetic biology.
 +
<p>Taking a step back, looking at the biotechnology field as a whole, many examples readily present themselves, in which products or services were offered or presented in ways which were incompatible with maintaining public trust. Among these are cases of pharmaceutical executives arbitrarily increasing the prices of lifesaving therapeutics by factors of several thousand percent, or the infamously unpopular patents of Genetic Use Restriction Technologies (GURT), better known as ‘terminator genes,’ which prevent farmers from reusing seed stocks for multiple generations [1]. According to Pew Research Center, 39% of Americans say that GM foods are worse for their health, compared to non-GM foods [2]. According to a 2016 Gallup Poll, 51% of Americans have a negative view of pharmaceutical companies [3]. ‘Big Pharma’ and ‘Big Ag’ are boogeymen that roll off the tongues of many Americans. And the stigma is even worse in other parts of the world.
 
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<p>A common criticism of biotech companies is that they act in ways agnostic or arrogantly unaware of what the public wants. To make sure that our project would not fall into the category of ‘well researched but completely unwanted,’ we made sure to consider from the beginning the specific cultural contexts in which our device would be used. This in turn, helped us narrow down our possible ideas, by beginning with a problem and a set of specific contexts, we were able to discard many possible project directions.
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<div style = 'padding-left:10%;padding-bottom: 22px; font-size: 20px; color: #d9a900'; ><b><i>Why not use whole organisms?</i></b></div>
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    <div id="Scientific Overview" style = 'padding-top: 30px;font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
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    Scientific Overview
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<div style = 'padding-right: 130PX; padding-left: 130PX; text-indent: 50px;line-height: 25px;' >   Before diving deep into the human elements which we considered when designing our project, we would like to give a basic overview of what we built, as it will allow us to return throughout this guide to specific features and examine how human practices informed our decision making.
 +
<p>We designed a mammalian cell-based bioassay that reports activation of specific stress pathways via fluorescence, for use in environmental toxicology. To do this, we selected transcriptionally regulated target genes which are present in mammalian cells and are involved in stress pathways (see figure 1 below). We isolated the promoters with transcription factor binding sites from these target genes and coupled them to a fluorescent reporter gene. We selected EGFP, a variant of green fluorescent protein (GFP). GFP is ubiquitous in synthetic biology due to its reliability and ease of measurement [4]. EGFP is derived from GFP, and has been optimized for use in mammalian systems. When a chemical of concern is screened using our assay, it will trigger a specific stress response, and the reporter gene will be expressed, causing the assay to fluoresce. The fluorescence of the assay can be quantitatively measured and analyzed. This assay will provide data on the effect of chemicals of concern on the physiological health of mammalian cells; measurements may be easily taken a range of concentrations, durations of exposure, salinities, pH, temperatures, nutrient availabilities, and other conditions. This also allows for measurement of synergistic or interfering effects due to multiple chemicals of concern present simultaneously.
 +
<p>
 +
  ////insert table////
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  We selected eight promoter constructs derived from five target genes and coupled them to EGFP. These promoter and reporter gene constructs were inserted into a plasmid and transfected into two cell lines, originating in mice (AML-12) and hamsters (CHO-DG44), respectively. The resulting bioassays were exposed to five different chemicals of concern at a variety of concentrations and conditions. Although human cell lines would make a superior model for human disease, compared to cell lines derived from hamsters and mice, for our project we chose not to use human cells, for reasons of safety, reproducibility by other teams, and the constraints of the competition.
 +
 
 +
</p>
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<p>
 +
A cell-based approach cannot replace in vivo toxicology studies. However these studies require extensive funding, time, and other resources. By developing a relatively low-cost, cell-based bioassay, preliminary data may be quickly gathered, allowing for more informed decision making as to which in vivo studies are necessary. By using a cell-based preliminary assay, it is our hope that researchers will be able to quickly gather data, make more informed decisions, and save resources. Our cell-based bioassay may also be used to add to the body of knowledge concerning the effect of specific chemicals of concern on the physiological health of mammalian cells and the mechanism of stress.
 +
</p>
 +
<p>We chose to use mammalian cells because they make much more accurate models for human health than bacteria or yeast. Furthermore, within the iGEM competition and the field of synthetic biology as a whole, there has been relatively little work with mammalian systems, compared to bacteria, yeast, and algae. Working with mammalian cells brings a variety of new challenges and opportunities to iGEM: they are more difficult and expensive to culture than bacteria, they require specialized equipment and safety training, they can be used to produce proteins suitable for use in human therapeutics, they can be used for more complicated circuits and pathways utilizing spatial/temporal differentiation, and they are much more sensitive to chemicals in the environment (allowing for more sensitive biosensors and bioassays).
 +
</p>
 +
 
  
<div style='padding-left:10%;padding-right: 7%'>A cell-based approach cannot replace in vivo toxicology studies. However these studies require extensive funding, time, and other resources. By developing a relatively low-cost, cell-based bioassay, preliminary data may be quickly gathered, allowing for more informed decision making as to which in vivo studies are necessary. By using a cell-based preliminary assay, it is our hope that researchers will be able to quickly gather data, make more informed decisions, and save resources. Our cell-based bioassay may also be used to add to the body of knowledge concerning the effect of specific chemicals of concern on the physiological health of mammalian cells and the mechanism of stress. </div>
 
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<div style = 'padding-left:10%;padding-bottom: 22px; font-size: 20px; color: #d9a900'; ><b><i>Why not use cell-free biochemical assays, such as ELISA?</i></b></div>
 
  
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  Antibody-based assays, such as Enzyme-Linked Immunosorbent Assay (ELISA), have been very successful in biomedical research, environmental toxicology, and other fields [2]. These cell-free methods involve selective binding of a target molecule to a prepared antibody. Such methods are very successful at identifying single, known compounds in an environmental sample, but do not provide any data regarding the effect of the chemical of concern on the health of a living cell. Similarly, the tools of analytical chemistry and organic chemistry may be used to great success when identifying molecules, but do not provide any data regarding the actual effect on a living cell.
 
 
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<div style = 'padding-left:10%;padding-bottom: 22px; font-size: 20px; color: #d9a900'; ><b><i>Why use synthetic biology?</i></b></div>
 
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The goal of our bioassay is to create a tool that can be used to better understand the effect on the physiological health of mammalian cells of environmental toxins. An alternative way to achieve this knowledge is to expose cells to the chemicals of concern, lyse the cells, isolate the RNA, and run a quantitative-real-time-reverse-transcription-PCR in order to characterize and quantify the mRNAs present in the cell. However, this approach has limitations. It necessarily involves lysing the cells, and cannot be used to gather real-time data about the behavior of the same cell over time. By using a fluorescent reporter gene, we can measure the induction of the reporter gene over time without lysing cells, and can more easily take a large number of data points across different chemicals of concern, concentrations, and other variables. A fluorescent bioassay also reduces the amount of work required to measure many data points, compared to PCR based methods. Our bioassay also makes possible the future study of the behavior of a single cell over time after exposure to a chemical of concern, with the aid of microfluidics.
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  <div id="Environmental Overview" style = 'padding-top: 30px;font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
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  Environmental Overview
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  </b></i>
 
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<div style = 'padding-left:10%;padding-bottom: 22px; font-size: 20px; color: #d9a900'; ><b><i>Why use mammalian cells?</i></b></div>
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   We chose to use mammalian cells because they make much more accurate models for human health than bacteria or yeast. Furthermore, within the iGEM competition and the field of synthetic biology as a whole, there has been relatively little work with mammalian systems, compared to bacteria, yeast, and algae. Working with mammalian cells brings a variety of new challenges and opportunities to iGEM: they are more difficult and expensive to culture than bacteria, they require specialized equipment and safety training, they can be used to produce proteins suitable for use in human therapeutics (due to similar most-translational modifications), they can be used for more complicated circuits and pathways utilizing spatial/temporal differentiation, and they are much more sensitive to chemicals in the environment (allowing for more sensitive biosensors and bioassays).
+
  Our team chose from the beginning to pursue the the environmental track of the iGEM competition. At the University of California, Davis, there is an established group of researchers who have been working with the EPA for the past 31 years to “acquire a better understanding of the human and ecological risks of hazardous substances; and advance the development of new technologies for the cleanup of contaminated sites” [11]. Our team had the opportunity to join UC Davis researchers on a trip to visit a Native American tribe in northern California who live on heavily polluted land.
 +
<p>
 +
  The tribe have reported unusually elevated rates of cancer and miscarriage incidence, and have indicated they have reason to suspect that the cause may be tied to environmental pollution on their tribal land from local agricultural and forestry corporations. Researchers from UC Davis have been collaborating with the tribe’s scientists and governing council to gather data pertaining to environmental and human health.
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 +
   The agricultural and forestry corporations in the region surrounding the tribe’s land are currently operating within legal regulations, however the tribe has indicated that these regulations are not as strict as they would like. One example a tribal member provided was that currently, herbicides may be applied within fifty feet of sources of drinking water. A concern is that this distance is not sufficient to prevent contamination of drinking water supplies. A variety of harmful chemicals have been found in the waters of the tribal lands, particularly microcystin toxins and organochlorine pesticides [12]. Analysis of water samples by the Young Lab at UC Davis in 2017 also found the presence of low concentrations of pharmaceuticals, including warfarin, in the waters of the tribal lands.
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 +
</p>
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<p>We were informed by tribal members that the members of the tribe interact with the flora, fauna, and water of the region regularly. These interactions take forms including the consumption of seafood, particularly salmon and shellfish, harvesting local plants and processing them to make baskets, swimming in the river, and ceremonies involving locally harvested materials.
 +
</p>
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<p>If the working hypothesis is found to be supported, that the tribe’s health crises are linked to environmental pollution of their lands and water, then the remedy would be to tighten regulations concerning the use of pesticides, herbicides, and other potentially harmful compounds. To affect such a significant policy change would require substantial scientific evidence, including careful in vivo studies. Our bioassay can serve as a tool with which to quickly and relatively cheaply acquire data which can be used to identity areas necessitating further study and inform which specific results to expect.
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</p>
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<p>If this working hypothesis is not supported by further study, alternative explanations for the tribe’s health crises should be explored, including predisposing genetic factors within the population and other factors. This possible explanation– that the tribe may experience elevated rates of specific diseases due to genetic predisposition– was suggested during the visit to a member of the tribe’s scientific body by a member of our team, and elicited a surprising response. The tribe’s scientist indicated that such a hypothesis would be very negatively received by the members of the tribe, for historical and cultural reasons. It would be perceived, the tribe’s scientist said, as an attempt to blame the tribe’s health problems on an inborn deficiency of the members, which given the persecution and genocide which the tribe underwent in the nineteenth and twentieth centuries, would strike a very powerful and negative chord. The scientist went on to reference several well publicised cases in which geneticists have squandered the trust of indigenous communities [13].
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</p>
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<p>
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  We selected several major environmental contaminants in the region for use in our project: copper sulfate, warfarin, 2,4-D, and metam sodium. These chemicals were selected based off their prevalence in the region, their negative impacts on human health, and the availability of use for our project. Additionally, we included hydrogen peroxide as a positive control, as it is easily obtained and causes oxidative stress to cells.
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<div style = 'padding-left:10%;padding-bottom: 22px; font-size: 20px; color: #d9a900'; ><b><i>Why not use human cells?</i></b></div>
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<div id="Cultural Context" style = 'padding-top: 30px;font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
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Cultural Context
  Although human cell lines would make a superior model for human disease, compared to cell lines derived from hamsters and mice, for our project we chose not to use human cells. Work involving human cells requires specialized facilities, equipment, resources, and safety training. Human cells require a BSL-2 lab, which would have been more difficult for our team to use than our regular wetlab space, which is BSL-1. Additionally, as our project took place in the context of the iGEM competition, we wanted for other teams to be able to easily reproduce our findings and expand them. By using human cell lines, many teams, which lack access to a BSL-2 lab, would have had more difficulty in expanding upon our project. It would be relatively straightforward to insert our genetic constructs to a human cell line, and this presents an opportunity to extend our project.
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<div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Promoter Constructs</b></div>
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  When our team was invited to join fellow UC Davis researchers to visit the Native American tribe, we were given training in ‘cultural competency.’ The purpose of this training was to educate the researchers, who as science professionals, had varying degrees of experience dealing with other communities, how best to behave to ensure that the tribe was treated with respect as a partner in research. The course was described in the prepared description of the site visit in the following manner:
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<p>“In this course, which will be preferably offered on-site in Yurok Country and feature YTEP and other Yurok tribal presenters, university researchers will be trained on tribal sovereignty, tribal intellectual property rights, trial history, tribal land and water rights, and on building effective collaboration with tribes. While the focus will be on working with the Yurok Tribe, the principles taught will be applicable to collaboration with other tribes and indigenous nations in the US and globally.”
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<p>At the site visit, the other researchers and our team were taught some of the history of the tribe by a member of the tribal leadership council. We were also taught some of the customs and ceremonies which the tribal members perform, particularly regarding the strong cultural connection between the members of the tribe, the land of the region, and the native flora and fauna.
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</p>
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<p>The team of UC Davis researchers included several professors of Native American Studies who helped the other researchers in questions of best practices regarding cultural competency in the course of their research. A key point of best practices we were told was to never claim the authority to say what another group does or does not believe, unless it is approved or previously expressed by an authority of the group. For example, it would not be acceptable to write on our iGEM wiki “the _______ tribe believes _______, therefore...” Any claims made about the beliefs or opinions of another group should be thoroughly grounded in verifiable evidence that the group does in fact hold these beliefs. For example, a claim may be supported by quoting a resolution or law passed by a body such as a tribal leadership council or another authorized body.
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</p>
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<p>At the first meeting, our team introduced ourselves to our fellow researchers, the tribe’s chief scientist, and members of the tribe. After we explained who we were and what the iGEM competition was, the tribe’s chief scientist said that she was familiar with some work being done regarding synthetic biology and bioremediation, and that a project involving release of genetically modified organisms would not be acceptable to the tribe. The iGEM competition as a whole has strict ‘NO RELEASE’ rules, however many projects are designed in such a way that the ultimate use-case for their product would require intentional release into the environment.
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</p>
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<p>Through the course of the cultural competency training and the site visit as a whole, a theme that resurfaced many times was a history of the tribe being taken advantage of by outsiders. Possibly due to this, many of the tribal members expressed skepticism of the intentions of outsiders. To paraphrase a comment made by a tribal member, “Plenty of people come to a tribe from a fancy university promising to fix things, and then they publish a few papers, get a few more letters after their name, and leave, but the problems haven’t gone away.” We were duly aware of this sentiment throughout the site visit, and took measures to ensure that we did not promise anything we could not fulfill, given the limited time and resources of the iGEM competition.
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</p>
  
Figure 1 shows the promoter constructs we used and the target genes from which they were derived. Full FASTA sequences for our promoters are available <a href= "https://2018.igem.org/Team:UC_Davis/SupplementalMaterials">here.</a>
 
 
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<div id="Political/Legislative Context" style = 'padding-top: 30px;font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
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Political/Legislative Context
    Figure 2. Promoter Constructs
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   In the United States, recognized Native American tribes are self-governing bodies, and have the power to make and enforce laws and regulations on their own lands. The specific Native American tribe which we visited has expressed their position on genetic engineering in an ordinance adopted in 2015, which may be accessed here [14]. In the ordinance, the tribe makes clear that they view the release of genetically modified organisms into their environment to be a major threat to their cultural values and traditional way of life. Compared to the United States as a whole, which has relatively tolerant laws regarding the production and use of genetically modified organisms, the tribe has far stricter laws.
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<p>
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Interestingly, within the ordinance, the tribe makes several exceptions. The first is unusual: “Genetically engineered or modified organisms do not include organisms created by traditional selective breeding, [...] or microorganisms created by moving genes or gene segments between unrelated bacteria” [14].  As much of biotechnology and synthetic biology uses bacteria as a host, we were surprised to find that the ordinance deemed the majority of the work done in the iGEM competition as acceptable.
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</p>
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<p>The ordinance also provides exceptions to the prohibition for “State or federally licensed medical research institutions, medical laboratories, or medical manufacturing facilities engaged in licensed medical production, or medical research involving genetically engineered or genetically modified organisms,” as well as for, “Educational or scientific institutes” [14]. This makes it appear that the major focus of the ordinance is to restrict agricultural biotechnology firms and their crops/livestock on tribal lands. The ordinance specifically refers to transgenic salmon– which are referred to as a threat to their way of life– and the significance of the wild salmon to the tribe’s cultural values.
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<p>We carefully considered the position taken by the tribe, concerning the introduction of genetically modified organisms as a threat to their cultural values and traditional way of life. While many arguments made by opponents of GMOs focus on perceived threats to human health, which can be settled empirically by careful in vivo studies, cultural arguments cannot be dismissed as easily. A community should have the right to live according their values and uphold traditional ways of life. If certain communities decide that their values are incompatible with the introduction of genetically modified organisms on to their land, then their decision should be respected.
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<p>The visit with the Native American tribe helped us focus our project and become aware of different sets of legal frameworks in which we operated. While working on the campus of our university, we were subject only to federal (America), state (California), and local (Yolo County, City of Davis, University of California) laws. If we were to return to test our device on tribal lands, we would be required to follow their specific ordinances and regulations, including seeking prior written permission to use genetically engineered devices for biomedical research. Likewise, it would be necessary to seek prior written permission before testing environmental samples taken from tribal lands. A similar procedure would be required when working with other communities.
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<div id="How We Proceeded" style = 'padding-top: 30px;font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
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How We Proceeded
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Evaluations
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Lessons Learned
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 +
Works Cited
 +
</b></i>
 +
</div>
 +
 
 +
<div style = 'padding-right: 130PX; padding-left: 130PX;line-height: 25px' >
 +
  [1] "An Ethical Examination of Genetic Use Restriction Technologies." November 20, 2008. Retrieved September 26, 2018. http://www.ethique.gouv.qc.ca/en/assets/documents/OGM/TRUG/TRUG-avis-EN.pdf.
 
<p></p>
 
<p></p>
  </div>
+
[2] Funk, Cary, and Brian Kennedy. “Public Opinion about Genetically Modified Foods and Trust in Scientists.” Pew Research Center: Internet, Science & Tech, Pew Research Center: Internet, Science & Tech, 1 Dec. 2016, www.pewinternet.org/2016/12/01/public-opinion-about-genetically-modified-foods-and-trust-in-scientists-connected-with-these-foods/.
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<table class="tg">
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<tr>
+
  <th class="tg-9hbo">Construct</th>
+
  <th class="tg-9hbo">Target Gene</th>
+
  <th class="tg-9hbo">Species of Origin</th>
+
  <th class="tg-9hbo">Stress Pathway</th>
+
  <th class="tg-9hbo">Size</th>
+
  <th class="tg-9hbo">Further Reading</th>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">MT1</td>
+
  <td class="tg-yw4l">Metallothionein 1</td>
+
  <td class="tg-yw4l">Mus musculus</td>
+
  <td class="tg-yw4l">Oxidative, heavy metal</td>
+
  <td class="tg-yw4l">305 nucleotides</td>
+
  <td class="tg-yw4l">[3]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">MT2_1</td>
+
  <td class="tg-yw4l">Metallothionein 2</td>
+
  <td class="tg-yw4l">Homo sapiens</td>
+
  <td class="tg-yw4l">Oxidative, heavy metal</td>
+
  <td class="tg-yw4l">377 nucleotides</td>
+
  <td class="tg-yw4l">[4]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">MT2_2</td>
+
  <td class="tg-yw4l">Metallothionein 2</td>
+
  <td class="tg-yw4l">Homo sapiens</td>
+
  <td class="tg-yw4l">Oxidative, heavy metal</td>
+
  <td class="tg-yw4l">59 nucleotides</td>
+
  <td class="tg-yw4l">[4]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">MT2_3</td>
+
  <td class="tg-yw4l">Metallothionein 2</td>
+
  <td class="tg-yw4l">Homo sapiens</td>
+
  <td class="tg-yw4l">Oxidative, heavy metal</td>
+
  <td class="tg-yw4l">60 nucleotides; construct MT2_2 plus one base at 5’ end</td>
+
  <td class="tg-yw4l">[4]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">MT2_4</td>
+
  <td class="tg-yw4l">Metallothionein 2</td>
+
  <td class="tg-yw4l">Homo sapiens</td>
+
  <td class="tg-yw4l">Oxidative, heavy metal</td>
+
  <td class="tg-yw4l">60 nucleotides; construct MT2_2 plus one base at 3’ end</td>
+
  <td class="tg-yw4l">[4]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">FGF</td>
+
  <td class="tg-yw4l">FGF21</td>
+
  <td class="tg-yw4l">Homo sapiens</td>
+
  <td class="tg-yw4l">Unfolded protein response (UPR), endoplasmic reticulum stress</td>
+
  <td class="tg-yw4l">695 nucleotides</td>
+
  <td class="tg-yw4l">[5]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">GD153</td>
+
  <td class="tg-yw4l">GADD153</td>
+
  <td class="tg-yw4l">Cricetulus griseus</td>
+
  <td class="tg-yw4l">Organochlorine biocides, genotoxins</td>
+
  <td class="tg-yw4l">811 nucleotides</td>
+
  <td class="tg-yw4l">[6], [7]</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">GD45</td>
+
  <td class="tg-yw4l">GADD45α</td>
+
  <td class="tg-yw4l">Homo sapiens</td>
+
  <td class="tg-yw4l">Genotoxins, mechanical stress</td>
+
  <td class="tg-yw4l">1006 nucleotides</td>
+
  <td class="tg-yw4l">[8]</td>
+
</tr>
+
</table>
+
    </center>
+
<div style='padding-top: 20px;'></div>
+
    <div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Host Strains</b></div>
+
    <div style='padding-top: 10px;'></div>
+
 
+
    <center>
+
      <div style = 'line-height: 25px' >
+
        Figure 3. Host Strains
+
    <p></p>
+
      </div>
+
  
     
+
<p></p>
      <style type="text/css">
+
[3] Gallup, Inc. “Restaurants Again Voted Most Popular U.S. Industry.” Gallup.com, 15 Aug. 2016, news.gallup.com/poll/194570/restaurants-again-voted-popular-industry.aspx.
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    <table class="tg">
+
    <tr>
+
      <th class="tg-9hbo">Host Strain</th>
+
      <th class="tg-9hbo">Description</th>
+
      <th class="tg-9hbo">Supplier</th>
+
    </tr>
+
    <tr>
+
      <td class="tg-yw4l">CHO-DG44</td>
+
      <td class="tg-yw4l">An immortal, adherent cell line derived from chinese hamster (Cricetulus griseus) ovary cells. The strain we used is dihydrofolate reductase deficient.</td>
+
      <td class="tg-yw4l">ATCC: CRL-9096 [16]</td>
+
    </tr>
+
    <tr>
+
      <td class="tg-yw4l">AML-12</td>
+
      <td class="tg-yw4l">An immortal, adherent cell line derived from mouse (Mus musculus) liver cells.</td>
+
      <td class="tg-yw4l">ATCC: CRL-2254 [17]</td>
+
    </tr>
+
    </table>
+
    </center>
+
<div style='padding-top: 20px;'></div>
+
    <div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Chemicals of Concern</b></div>
+
    <div style='padding-top: 10px;'></div>
+
 
+
    <center>
+
      <div style = 'line-height: 25px' >
+
        Figure 4. Chemicals of Concern
+
    <p></p>
+
      </div>
+
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+
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+
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+
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+
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+
  <div style='padding-top: 20px;'></div>
+
  <th class="tg-9hbo">Chemical of Concern</th>
+
  <th class="tg-9hbo">Class</th>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">Copper Sulfate</td>
+
  <td class="tg-yw4l">Heavy metal</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">Zinc Sulfate</td>
+
  <td class="tg-yw4l">Heavy metal</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">2,4-D</td>
+
  <td class="tg-yw4l">Organochlorine herbicide</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">Warfarin</td>
+
  <td class="tg-yw4l">Pharmaceutical anticoagulant, pesticide</td>
+
</tr>
+
<tr>
+
  <td class="tg-yw4l">Hydrogen Peroxide</td>
+
  <td class="tg-yw4l">Oxidizing agent</td>
+
</tr>
+
</table>
+
</center>
+
  
 +
<p></p>
 +
[4]  “PDB101: Molecule of the Month: Green Fluorescent Protein (GFP).” PDB-101, RCSB PDB, June 2003, pdb101.rcsb.org/motm/42.
  
<div style='padding-top: 20px;'></div>
+
<p></p>
<div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Plasmid</b></div>
+
[5] Larochelle, Olivier & Labbé, Simon & Harrisson, Jean-François & Simard, Carl & Tremblay, Véronique & St-Gelais, Geneviève & Govindan, Manjapra Variath & Seguin, Carl. (2008). Nuclear Factor-1 and Metal Transcription Factor-1 Synergistically Activate the Mouse Metallothionein-1 Gene in Response to Metal Ions. The Journal of biological chemistry. 283. 8190-201. 10.1074/jbc.M800640200.
<div style='padding-top: 10px;'></div>
+
<div style='padding-left:7%;padding-right: 7%'>
+
  We used pcDNA3-EGFP as our plasmid [11]. The original plasmid is shown in Figure 5 below.
+
  
</div>
+
<p></p>
<div style='padding-top: 10px;'></div>
+
[6] Santos, Anderson K. et al. "Expression System Based On An Mtiia Promoter To Produce Hpsa In Mammalian Cell Cultures". Frontiers In Microbiology, vol 7, 2016. Frontiers Media SA, doi:10.3389/fmicb.2016.01280.
<center>
+
  <div style = 'line-height: 25px' >
+
    Figure 5. Map of pcDNA3-EGFP [12]
+
  
 
<p></p>
 
<p></p>
  </div>
+
[7] F.G. Schaap, A.E. Kremer, W.H. Lamers, P.L. Jansen, I.C. Gaemers. Fibroblast growth factor 21 is induced by endoplasmic reticulum stress
  <img src="https://static.igem.org/mediawiki/2018/b/b4/T--UC_Davis--PM1c.png" alt="Plasmid map 1" style="width: 40%; margin-left: auto;margin-right: auto;" ;Padding: "0";>
+
Biochimie, 95 (2013), pp. 692-699, 10.1016/j.biochi.2012.10.019
</center>
+
<div style='padding-left:7%;padding-right: 7%'>
+
  To prepare our constructs, we used restriction enzymes to remove the CMV enhancer, CMV promoter, and the T7 promoter. Promoter sequences were inserted using either restriction digest or Sequence and Ligation Independent Cloning (SLIC). Figure 6 below shows the complete plasmid for construct MT2_1.
+
  
</div>
+
<p></p>
<center>
+
[8]  Li, Dahui et al. "Genotoxic Evaluation Of The Insecticide Endosulfan Based On The Induced GADD153-GFP Reporter Gene Expression". Environmental Monitoring And Assessment, vol 176, no. 1-4, 2010, pp. 251-258. Springer Nature, doi:10.1007/s10661-010-1580-7.
  <div style = 'line-height: 25px' >
+
    Figure 6. Map of pcDNA-EGFP_MT2_2 [12]
+
  
 
<p></p>
 
<p></p>
  </div>
+
[9]  Park, Jong Sung et al. "Isolation, Characterization And Chromosomal Localization Of The Human GADD153 Gene". Gene, vol 116, no. 2, 1992, pp. 259-267. Elsevier BV, doi:10.1016/0378-1119(92)90523-r.
  <img src="https://static.igem.org/mediawiki/2018/f/fa/T--UC_Davis--PM2.png" alt="Plasmid map 2" style="width: 40%; margin-left: auto;margin-right: auto;" ;Padding: "0";>
+
</center>
+
  
 +
<p></p>
 +
[10] Mitra, Sumegha et al. "Gadd45a Promoter Regulation By A Functional Genetic Variant Associated With Acute Lung Injury". Plos ONE, vol 9, no. 6, 2014, p. e100169. Public Library Of Science (Plos), doi:10.1371/journal.pone.0100169.
 +
 +
<p></p>
 +
[11] "UC Davis Superfund Research Program". UC Davis Superfund Research Program, 2018, https://www.superfund.ucdavis.edu/. Accessed 1 Aug 2018.
 +
 +
<p></p>
 +
[12] Eagles-Smith, C.A., and B.L. Johnson, 2012, Contaminants in the Klamath Basin: Historical patterns, current distribution, and data gap identification: U.S. Geological Survey Administrative Report, 88 p.
 +
 +
<p></p>
 +
[13] For a look at some of these cases, the following article references several of the most publicised times genetics researchers have lost goodwill with Indigenous peoples. “Ancient Genome Stirs Ethics Debate.” Nature News, Nature Publishing Group, www.nature.com/news/ancient-genome-stirs-ethics-debate-1.14698.
 +
 +
<p></p>
 +
[14] “Ch. 21.15 Genetically Engineered Organisms | Yurok Tribal Code.” Yurok Tribe Tribal Code, Yurok Tribe, 10 Dec. 2015, yurok.tribal.codes/YTC/21.15.
 +
 +
<p></p>
 +
[15]“Human Practices.” iGEM Foundation, igem.org/Human_Practices .
 +
 +
<p></p>
 +
[16] “iGEM Medals.” iGEM Foundation, https://2018.igem.org/Judging/Medals .
  
<div style='padding-top: 20px;'></div>
 
<div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Measurement</b></div>
 
<div style='padding-top: 10px;'></div>
 
<div style='padding-left:7%;padding-right: 7%'>
 
  Our bioassay was constructed on 96 well plates. Plates were seeded with 30,000 cells/well for AML12 cells and 20,000 cells/well for CHO cells and allowed to adhere for 24 hours. The cells were seeded such that 24 hours after reaching they would be at 70%-90% confluence. At this time, we transfected our cells with the target promoter and allowed to sit for another 24 hours. Next, the complete growth media present in the wells were aspirated and replaced with clear media containing chemical of concern. Testing for fluorescence was done using a Tecan microplate reader at an interval of every 4 hours for a 24 hours period.
 
</div>
 
  
<div style='padding-top: 20px;'></div>
 
<div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>Extensions</b></div>
 
<div style='padding-top: 10px;'></div>
 
<div style='padding-left:7%;padding-right: 7%'>
 
  Our project opens up new opportunities for work with mammalian cells in the iGEM competition. By adding new mammalian parts to the registry, future teams will have the ability to easily access useful mammalian regulatory elements for use in their own constructs. Future teams may also benefit from our protocol for measuring fluorescence of adherent mammalian cells. One extension of our work is to transfect our construct into human cell lines. By using human cells, the bioassay will be a more accurate model for human health.
 
 
</div>
 
</div>
  
<div style='padding-top: 20px;'></div>
+
<div id="Appendix" style = 'padding-top: 30px;font-size: 20px;color: #667d9d; padding-right: 130PX; padding-left: 130PX;line-height: 25px; padding-bottom: 20px;' ><b><i>
<div style = 'padding-left:7%;padding-bottom: 22px; font-size: 25px; color: #667d9d'; ><b>References</b></div>
+
Appendix
<div style='padding-top: 10px;'></div>
+
</b></i>
<div style='padding-left:7%;padding-right: 7%'>
+
  [1] “PDB101: Molecule of the Month: Green Fluorescent Protein (GFP).” PDB-101, RCSB PDB, June 2003, pdb101.rcsb.org/motm/42.
+
      <p></p>
+
      [2] Enzyme Immunoassay (EIA)/Enzyme-Linked Immunosorbent Assay (ELISA)
+
      Rudolf M. Lequin
+
      Clinical Chemistry Dec 2005, 51 (12) 2415-2418; DOI: 10.1373/clinchem.2005.051532
+
      <p></p>
+
      [3] Larochelle, Olivier & Labbé, Simon & Harrisson, Jean-François & Simard, Carl & Tremblay, Véronique & St-Gelais, Geneviève & Govindan, Manjapra Variath & Seguin, Carl. (2008). Nuclear Factor-1 and Metal Transcription Factor-1 Synergistically Activate the Mouse Metallothionein-1 Gene in Response to Metal Ions. The Journal of biological chemistry. 283. 8190-201. 10.1074/jbc.M800640200.
+
      <p></p>
+
[4] Santos, Anderson K. et al. "Expression System Based On An Mtiia Promoter To Produce Hpsa In Mammalian Cell Cultures". Frontiers In Microbiology, vol 7, 2016. Frontiers Media SA, doi:10.3389/fmicb.2016.01280.
+
      <p></p>
+
      [5] F.G. Schaap, A.E. Kremer, W.H. Lamers, P.L. Jansen, I.C. Gaemers. Fibroblast growth factor 21 is induced by endoplasmic reticulum stress
+
      Biochimie, 95 (2013), pp. 692-699, 10.1016/j.biochi.2012.10.019
+
      <p></p>
+
      [6]  Li, Dahui et al. "Genotoxic Evaluation Of The Insecticide Endosulfan Based On The Induced GADD153-GFP Reporter Gene Expression". Environmental Monitoring And Assessment, vol 176, no. 1-4, 2010, pp. 251-258. Springer Nature, doi:10.1007/s10661-010-1580-7.
+
      <p></p>
+
      [7]  Park, Jong Sung et al. "Isolation, Characterization And Chromosomal Localization Of The Human GADD153 Gene". Gene, vol 116, no. 2, 1992, pp. 259-267. Elsevier BV, doi:10.1016/0378-1119(92)90523-r.
+
      <p></p>
+
      [8] Mitra, Sumegha et al. "Gadd45a Promoter Regulation By A Functional Genetic Variant Associated With Acute Lung Injury". Plos ONE, vol 9, no. 6, 2014, p. e100169. Public Library Of Science (Plos), doi:10.1371/journal.pone.0100169.
+
      <p></p>
+
      [9] Cell line available from ATCC at: https://www.atcc.org/Products/All/CRL-9096.aspx
+
      <p></p>
+
      [10] Cell line available from ATCC at: https://www.atcc.org/products/all/CRL-2254.aspx
+
      <p></p>
+
      [11] More detailed information regarding this plasmid is available from Addgene here: https://www.addgene.org/13031/ . pcDNA3-EGFP was a gift from Doug Golenbock (Addgene plasmid # 13031)
+
      <p></p>
+
      [12] Plasmid map created with software from SnapGene. Software is available at: snapgene.com
+
     
+
 
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Revision as of 16:57, 3 October 2018

iGEM

Human_Practices
Integrating Human Practices
Introduction
A guiding theme which we returned to again and again, as we designed our project, was the awareness that science does not happen in a vacuum. Science and technology exist within social frameworks– public policy, economics, public opinion, and overall acceptance of a new innovation are crucial factors to consider. A well researched, well tested product can and will fail the essential test of ‘usefulness’ if external social factors are disregarded. A product that the public will not accept and use is a poorly designed product. This is especially true within the field of synthetic biology.

Taking a step back, looking at the biotechnology field as a whole, many examples readily present themselves, in which products or services were offered or presented in ways which were incompatible with maintaining public trust. Among these are cases of pharmaceutical executives arbitrarily increasing the prices of lifesaving therapeutics by factors of several thousand percent, or the infamously unpopular patents of Genetic Use Restriction Technologies (GURT), better known as ‘terminator genes,’ which prevent farmers from reusing seed stocks for multiple generations [1]. According to Pew Research Center, 39% of Americans say that GM foods are worse for their health, compared to non-GM foods [2]. According to a 2016 Gallup Poll, 51% of Americans have a negative view of pharmaceutical companies [3]. ‘Big Pharma’ and ‘Big Ag’ are boogeymen that roll off the tongues of many Americans. And the stigma is even worse in other parts of the world.

A common criticism of biotech companies is that they act in ways agnostic or arrogantly unaware of what the public wants. To make sure that our project would not fall into the category of ‘well researched but completely unwanted,’ we made sure to consider from the beginning the specific cultural contexts in which our device would be used. This in turn, helped us narrow down our possible ideas, by beginning with a problem and a set of specific contexts, we were able to discard many possible project directions.

Scientific Overview
Before diving deep into the human elements which we considered when designing our project, we would like to give a basic overview of what we built, as it will allow us to return throughout this guide to specific features and examine how human practices informed our decision making.

We designed a mammalian cell-based bioassay that reports activation of specific stress pathways via fluorescence, for use in environmental toxicology. To do this, we selected transcriptionally regulated target genes which are present in mammalian cells and are involved in stress pathways (see figure 1 below). We isolated the promoters with transcription factor binding sites from these target genes and coupled them to a fluorescent reporter gene. We selected EGFP, a variant of green fluorescent protein (GFP). GFP is ubiquitous in synthetic biology due to its reliability and ease of measurement [4]. EGFP is derived from GFP, and has been optimized for use in mammalian systems. When a chemical of concern is screened using our assay, it will trigger a specific stress response, and the reporter gene will be expressed, causing the assay to fluoresce. The fluorescence of the assay can be quantitatively measured and analyzed. This assay will provide data on the effect of chemicals of concern on the physiological health of mammalian cells; measurements may be easily taken a range of concentrations, durations of exposure, salinities, pH, temperatures, nutrient availabilities, and other conditions. This also allows for measurement of synergistic or interfering effects due to multiple chemicals of concern present simultaneously.

////insert table//// We selected eight promoter constructs derived from five target genes and coupled them to EGFP. These promoter and reporter gene constructs were inserted into a plasmid and transfected into two cell lines, originating in mice (AML-12) and hamsters (CHO-DG44), respectively. The resulting bioassays were exposed to five different chemicals of concern at a variety of concentrations and conditions. Although human cell lines would make a superior model for human disease, compared to cell lines derived from hamsters and mice, for our project we chose not to use human cells, for reasons of safety, reproducibility by other teams, and the constraints of the competition.

A cell-based approach cannot replace in vivo toxicology studies. However these studies require extensive funding, time, and other resources. By developing a relatively low-cost, cell-based bioassay, preliminary data may be quickly gathered, allowing for more informed decision making as to which in vivo studies are necessary. By using a cell-based preliminary assay, it is our hope that researchers will be able to quickly gather data, make more informed decisions, and save resources. Our cell-based bioassay may also be used to add to the body of knowledge concerning the effect of specific chemicals of concern on the physiological health of mammalian cells and the mechanism of stress.

We chose to use mammalian cells because they make much more accurate models for human health than bacteria or yeast. Furthermore, within the iGEM competition and the field of synthetic biology as a whole, there has been relatively little work with mammalian systems, compared to bacteria, yeast, and algae. Working with mammalian cells brings a variety of new challenges and opportunities to iGEM: they are more difficult and expensive to culture than bacteria, they require specialized equipment and safety training, they can be used to produce proteins suitable for use in human therapeutics, they can be used for more complicated circuits and pathways utilizing spatial/temporal differentiation, and they are much more sensitive to chemicals in the environment (allowing for more sensitive biosensors and bioassays).

Environmental Overview
Our team chose from the beginning to pursue the the environmental track of the iGEM competition. At the University of California, Davis, there is an established group of researchers who have been working with the EPA for the past 31 years to “acquire a better understanding of the human and ecological risks of hazardous substances; and advance the development of new technologies for the cleanup of contaminated sites” [11]. Our team had the opportunity to join UC Davis researchers on a trip to visit a Native American tribe in northern California who live on heavily polluted land.

The tribe have reported unusually elevated rates of cancer and miscarriage incidence, and have indicated they have reason to suspect that the cause may be tied to environmental pollution on their tribal land from local agricultural and forestry corporations. Researchers from UC Davis have been collaborating with the tribe’s scientists and governing council to gather data pertaining to environmental and human health.

The agricultural and forestry corporations in the region surrounding the tribe’s land are currently operating within legal regulations, however the tribe has indicated that these regulations are not as strict as they would like. One example a tribal member provided was that currently, herbicides may be applied within fifty feet of sources of drinking water. A concern is that this distance is not sufficient to prevent contamination of drinking water supplies. A variety of harmful chemicals have been found in the waters of the tribal lands, particularly microcystin toxins and organochlorine pesticides [12]. Analysis of water samples by the Young Lab at UC Davis in 2017 also found the presence of low concentrations of pharmaceuticals, including warfarin, in the waters of the tribal lands.

We were informed by tribal members that the members of the tribe interact with the flora, fauna, and water of the region regularly. These interactions take forms including the consumption of seafood, particularly salmon and shellfish, harvesting local plants and processing them to make baskets, swimming in the river, and ceremonies involving locally harvested materials.

If the working hypothesis is found to be supported, that the tribe’s health crises are linked to environmental pollution of their lands and water, then the remedy would be to tighten regulations concerning the use of pesticides, herbicides, and other potentially harmful compounds. To affect such a significant policy change would require substantial scientific evidence, including careful in vivo studies. Our bioassay can serve as a tool with which to quickly and relatively cheaply acquire data which can be used to identity areas necessitating further study and inform which specific results to expect.

If this working hypothesis is not supported by further study, alternative explanations for the tribe’s health crises should be explored, including predisposing genetic factors within the population and other factors. This possible explanation– that the tribe may experience elevated rates of specific diseases due to genetic predisposition– was suggested during the visit to a member of the tribe’s scientific body by a member of our team, and elicited a surprising response. The tribe’s scientist indicated that such a hypothesis would be very negatively received by the members of the tribe, for historical and cultural reasons. It would be perceived, the tribe’s scientist said, as an attempt to blame the tribe’s health problems on an inborn deficiency of the members, which given the persecution and genocide which the tribe underwent in the nineteenth and twentieth centuries, would strike a very powerful and negative chord. The scientist went on to reference several well publicised cases in which geneticists have squandered the trust of indigenous communities [13].

We selected several major environmental contaminants in the region for use in our project: copper sulfate, warfarin, 2,4-D, and metam sodium. These chemicals were selected based off their prevalence in the region, their negative impacts on human health, and the availability of use for our project. Additionally, we included hydrogen peroxide as a positive control, as it is easily obtained and causes oxidative stress to cells.

Cultural Context
When our team was invited to join fellow UC Davis researchers to visit the Native American tribe, we were given training in ‘cultural competency.’ The purpose of this training was to educate the researchers, who as science professionals, had varying degrees of experience dealing with other communities, how best to behave to ensure that the tribe was treated with respect as a partner in research. The course was described in the prepared description of the site visit in the following manner:

“In this course, which will be preferably offered on-site in Yurok Country and feature YTEP and other Yurok tribal presenters, university researchers will be trained on tribal sovereignty, tribal intellectual property rights, trial history, tribal land and water rights, and on building effective collaboration with tribes. While the focus will be on working with the Yurok Tribe, the principles taught will be applicable to collaboration with other tribes and indigenous nations in the US and globally.”

At the site visit, the other researchers and our team were taught some of the history of the tribe by a member of the tribal leadership council. We were also taught some of the customs and ceremonies which the tribal members perform, particularly regarding the strong cultural connection between the members of the tribe, the land of the region, and the native flora and fauna.

The team of UC Davis researchers included several professors of Native American Studies who helped the other researchers in questions of best practices regarding cultural competency in the course of their research. A key point of best practices we were told was to never claim the authority to say what another group does or does not believe, unless it is approved or previously expressed by an authority of the group. For example, it would not be acceptable to write on our iGEM wiki “the _______ tribe believes _______, therefore...” Any claims made about the beliefs or opinions of another group should be thoroughly grounded in verifiable evidence that the group does in fact hold these beliefs. For example, a claim may be supported by quoting a resolution or law passed by a body such as a tribal leadership council or another authorized body.

At the first meeting, our team introduced ourselves to our fellow researchers, the tribe’s chief scientist, and members of the tribe. After we explained who we were and what the iGEM competition was, the tribe’s chief scientist said that she was familiar with some work being done regarding synthetic biology and bioremediation, and that a project involving release of genetically modified organisms would not be acceptable to the tribe. The iGEM competition as a whole has strict ‘NO RELEASE’ rules, however many projects are designed in such a way that the ultimate use-case for their product would require intentional release into the environment.

Through the course of the cultural competency training and the site visit as a whole, a theme that resurfaced many times was a history of the tribe being taken advantage of by outsiders. Possibly due to this, many of the tribal members expressed skepticism of the intentions of outsiders. To paraphrase a comment made by a tribal member, “Plenty of people come to a tribe from a fancy university promising to fix things, and then they publish a few papers, get a few more letters after their name, and leave, but the problems haven’t gone away.” We were duly aware of this sentiment throughout the site visit, and took measures to ensure that we did not promise anything we could not fulfill, given the limited time and resources of the iGEM competition.

Political/Legislative Context
In the United States, recognized Native American tribes are self-governing bodies, and have the power to make and enforce laws and regulations on their own lands. The specific Native American tribe which we visited has expressed their position on genetic engineering in an ordinance adopted in 2015, which may be accessed here [14]. In the ordinance, the tribe makes clear that they view the release of genetically modified organisms into their environment to be a major threat to their cultural values and traditional way of life. Compared to the United States as a whole, which has relatively tolerant laws regarding the production and use of genetically modified organisms, the tribe has far stricter laws.

Interestingly, within the ordinance, the tribe makes several exceptions. The first is unusual: “Genetically engineered or modified organisms do not include organisms created by traditional selective breeding, [...] or microorganisms created by moving genes or gene segments between unrelated bacteria” [14]. As much of biotechnology and synthetic biology uses bacteria as a host, we were surprised to find that the ordinance deemed the majority of the work done in the iGEM competition as acceptable.

The ordinance also provides exceptions to the prohibition for “State or federally licensed medical research institutions, medical laboratories, or medical manufacturing facilities engaged in licensed medical production, or medical research involving genetically engineered or genetically modified organisms,” as well as for, “Educational or scientific institutes” [14]. This makes it appear that the major focus of the ordinance is to restrict agricultural biotechnology firms and their crops/livestock on tribal lands. The ordinance specifically refers to transgenic salmon– which are referred to as a threat to their way of life– and the significance of the wild salmon to the tribe’s cultural values.

We carefully considered the position taken by the tribe, concerning the introduction of genetically modified organisms as a threat to their cultural values and traditional way of life. While many arguments made by opponents of GMOs focus on perceived threats to human health, which can be settled empirically by careful in vivo studies, cultural arguments cannot be dismissed as easily. A community should have the right to live according their values and uphold traditional ways of life. If certain communities decide that their values are incompatible with the introduction of genetically modified organisms on to their land, then their decision should be respected.

The visit with the Native American tribe helped us focus our project and become aware of different sets of legal frameworks in which we operated. While working on the campus of our university, we were subject only to federal (America), state (California), and local (Yolo County, City of Davis, University of California) laws. If we were to return to test our device on tribal lands, we would be required to follow their specific ordinances and regulations, including seeking prior written permission to use genetically engineered devices for biomedical research. Likewise, it would be necessary to seek prior written permission before testing environmental samples taken from tribal lands. A similar procedure would be required when working with other communities.

How We Proceeded
Evaluations
Lessons Learned
Works Cited
[1] "An Ethical Examination of Genetic Use Restriction Technologies." November 20, 2008. Retrieved September 26, 2018. http://www.ethique.gouv.qc.ca/en/assets/documents/OGM/TRUG/TRUG-avis-EN.pdf.

[2] Funk, Cary, and Brian Kennedy. “Public Opinion about Genetically Modified Foods and Trust in Scientists.” Pew Research Center: Internet, Science & Tech, Pew Research Center: Internet, Science & Tech, 1 Dec. 2016, www.pewinternet.org/2016/12/01/public-opinion-about-genetically-modified-foods-and-trust-in-scientists-connected-with-these-foods/.

[3] Gallup, Inc. “Restaurants Again Voted Most Popular U.S. Industry.” Gallup.com, 15 Aug. 2016, news.gallup.com/poll/194570/restaurants-again-voted-popular-industry.aspx.

[4] “PDB101: Molecule of the Month: Green Fluorescent Protein (GFP).” PDB-101, RCSB PDB, June 2003, pdb101.rcsb.org/motm/42.

[5] Larochelle, Olivier & Labbé, Simon & Harrisson, Jean-François & Simard, Carl & Tremblay, Véronique & St-Gelais, Geneviève & Govindan, Manjapra Variath & Seguin, Carl. (2008). Nuclear Factor-1 and Metal Transcription Factor-1 Synergistically Activate the Mouse Metallothionein-1 Gene in Response to Metal Ions. The Journal of biological chemistry. 283. 8190-201. 10.1074/jbc.M800640200.

[6] Santos, Anderson K. et al. "Expression System Based On An Mtiia Promoter To Produce Hpsa In Mammalian Cell Cultures". Frontiers In Microbiology, vol 7, 2016. Frontiers Media SA, doi:10.3389/fmicb.2016.01280.

[7] F.G. Schaap, A.E. Kremer, W.H. Lamers, P.L. Jansen, I.C. Gaemers. Fibroblast growth factor 21 is induced by endoplasmic reticulum stress Biochimie, 95 (2013), pp. 692-699, 10.1016/j.biochi.2012.10.019

[8] Li, Dahui et al. "Genotoxic Evaluation Of The Insecticide Endosulfan Based On The Induced GADD153-GFP Reporter Gene Expression". Environmental Monitoring And Assessment, vol 176, no. 1-4, 2010, pp. 251-258. Springer Nature, doi:10.1007/s10661-010-1580-7.

[9] Park, Jong Sung et al. "Isolation, Characterization And Chromosomal Localization Of The Human GADD153 Gene". Gene, vol 116, no. 2, 1992, pp. 259-267. Elsevier BV, doi:10.1016/0378-1119(92)90523-r.

[10] Mitra, Sumegha et al. "Gadd45a Promoter Regulation By A Functional Genetic Variant Associated With Acute Lung Injury". Plos ONE, vol 9, no. 6, 2014, p. e100169. Public Library Of Science (Plos), doi:10.1371/journal.pone.0100169.

[11] "UC Davis Superfund Research Program". UC Davis Superfund Research Program, 2018, https://www.superfund.ucdavis.edu/. Accessed 1 Aug 2018.

[12] Eagles-Smith, C.A., and B.L. Johnson, 2012, Contaminants in the Klamath Basin: Historical patterns, current distribution, and data gap identification: U.S. Geological Survey Administrative Report, 88 p.

[13] For a look at some of these cases, the following article references several of the most publicised times genetics researchers have lost goodwill with Indigenous peoples. “Ancient Genome Stirs Ethics Debate.” Nature News, Nature Publishing Group, www.nature.com/news/ancient-genome-stirs-ethics-debate-1.14698.

[14] “Ch. 21.15 Genetically Engineered Organisms | Yurok Tribal Code.” Yurok Tribe Tribal Code, Yurok Tribe, 10 Dec. 2015, yurok.tribal.codes/YTC/21.15.

[15]“Human Practices.” iGEM Foundation, igem.org/Human_Practices .

[16] “iGEM Medals.” iGEM Foundation, https://2018.igem.org/Judging/Medals .
Appendix
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UC Davis iGEM 2018