Difference between revisions of "Team:Tec-Monterrey/Description"
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| − | Here is where our beloved <h4 class="celeste">CRISPR-Cas</h4> complex comes into place. (Figure | + | Here is where our beloved <h4 class="celeste">CRISPR-Cas</h4> complex comes into place. (Figure 4) |
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<h4 class="celeste">CRISPR-Cas</h4> is a prokaryotic immune system that protects bacteria from phages and plasmids. With this complex, <b>foreign DNA</b>, in the form of <b><i>spacers</i></b>, is incorporated into the bacteria’s genome, specifically at the CRISPR locus. This <b><i>acquisition</i></b> of new DNA generates a memory of each “infection”. | <h4 class="celeste">CRISPR-Cas</h4> is a prokaryotic immune system that protects bacteria from phages and plasmids. With this complex, <b>foreign DNA</b>, in the form of <b><i>spacers</i></b>, is incorporated into the bacteria’s genome, specifically at the CRISPR locus. This <b><i>acquisition</i></b> of new DNA generates a memory of each “infection”. | ||
Revision as of 01:30, 18 October 2018
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Overview
CRISPR-Cas technology has the capability of storing information. This year, iGEM team Tec-Monterrey aims to use the CRISPR-Cas system to store specific DNA sequences in the genome of E. coli in order to save information about the environment surrounding the bacteria. To make this possible, Cas1-Cas2 proteins, which create the protospacer acquisition in the CRISPR system, are used to insert a synthetic DNA sequence in the CRISPR array within the genome of the bacteria. This synthetic sequence is produced by a second system, called SCRIBE. The final step of our project is reading out the inserted DNA sequence. Specific primers for polymerase chain reaction (PCR) are used to amplify a section of the CRISPR array where the sequence is inserted. Taking together both systems, our project intends to act as a biological tape recorder capable of sensing external stimuli in the environment and storing their presence in the genome.
System Functionality
The construct shown in Figure 1 codes for the SCRIBE system adaptation.
This system generates single-stranded DNA inside of living cells in response to gene regulatory signals.
It is composed of 3 main components:
This system generates single-stranded DNA inside of living cells in response to gene regulatory signals.
It is composed of 3 main components:
- A reverse transcriptase protein
-
One
msr
RNA moiety which acts as a primer for the RT. -
A second RNA moiety, called
msd
, which represents a template for the reverse transcriptase. This sequence contains themessage of interest
.
Figure 2: Retrotranscriptase action
This hybrid
This message has a PAM sequence, a crucial component for the identification by the CRISPR-Cas complex. (Figure 3)
RNA-ssDNA
molecule contains themessage of interest
.This message has a PAM sequence, a crucial component for the identification by the CRISPR-Cas complex. (Figure 3)
Figure 4: Cas 1 and Cas 2 construct
These proteins (Figure 5) have to detect the PAM sequence in order to enable their function as endonucleases, in other words, their activity to work as scissors that cut DNA sequences.
Figure 6: Message insertion
Figure 1: Construct for SCRIBE system
Then, the retrotranscriptase acts on the
msd
(RNA) sequence and produces a hybrid RNA-ssDNA molecule calledmsDNA
, as shown in Figure 2.
Figure 3: Message acquisition by Cas proteins
Here is where our beloved
Several Cas proteins are involved in this system, but Cas1 and Cas2 are the only proteins needed for acquisition of new spacers.
CRISPR-Cas
complex comes into place. (Figure 4)CRISPR-Cas
is a prokaryotic immune system that protects bacteria from phages and plasmids. With this complex, foreign DNA, in the form of spacers, is incorporated into the bacteria’s genome, specifically at the CRISPR locus. This acquisition of new DNA generates a memory of each “infection”.Several Cas proteins are involved in this system, but Cas1 and Cas2 are the only proteins needed for acquisition of new spacers.
Figure 5: Cas 1 and Cas 2 complex
Once the PAM sequence is detected, the Cas1-Cas2 complex cuts the target sequence and integrates it into the bacteria’s genome, as shown in Figure 6.
References
Amlinger, L., Hoekzema, M., Wagner, E. G. H., Koskiniemi, S. & Lundgren, M. Fluorescent CRISPR Adaptation Reporter for rapid quantification of spacer acquisition. (2017).doi: 10.1038/s41598-017-10876-z.
Díez-Villaseñor, C., Guzmán, N. M., Almendros, C., García-Martínez, J. & Mojica, F. J. M. CRISPR-spacer integration reporter plasmids reveal distinct genuine acquisition specificities among CRISPR-Cas I-E variants of Escherichia coli. RNA Biol. (2013). doi:10.4161/rna.24023
Farzadfard, F., & Lu, T. K. Genomically encoded analog memory with precise in vivo DNA writing in living cell populations. Science. (2014). doi: 10.1126/science.1256272.
Levy, A., Goren, M. G., Yosef, I., Auster, O., Manor, M., Amitai, G., Edgar, R., Qimron, U. & Sorek, R. CRISPR adaptation biases explain preference for acquisition of foreign DNA. Nature. (2015). doi:10.1038/nature14302
Nuñez, J. K. Mechanism of CRISPR–Cas Immunological Memory. (2016). Doctoral dissertation, UC Berkeley
Nuñez, J. K., Kranzusch P, Noeske J, Wright A, Davies C, Doudna J. Cas1-Cas2 complex formation mediates spacer acquisition during CRISPR-Cas adaptive immunity. Nat. Struct. Mol. Biol. (2014). doi:10.1038/nsmb.2820
Sheth, R. U., Yim, S. S., Wu, F. L. & Wang, H. H. Multiplex recording of cellular events over time on CRISPR biological tape. Science. (2017). doi:10.1126/science.aao0958
Shipman, S. L., Nivala, J., Macklis, J. D., & Church, G. M. Molecular recordings by directed CRISPR spacer acquisition. Science. (2016). doi: 10.1126/science.aaf1175
Tang, W., & Liu, D. R. Rewritable multi-event analog recording in bacterial and mammalian cells. Science. (2018). doi: 10.1126/science.aap8992