There is yet to exist a system that can make specific Cytidine (C) to Uridine (U) edits on mRNA, which can be accomplished through a deamination process (Figure 1). APOBEC, a cytidine deaminase enzyme, is a well-established protein which is known to perform C to U conversions on RNA strands (Smith, Bennett, Kizilyer, McDougall & Prohaska, 2012). Therefore, we intend to fuse an RNA-targeting Cas13 to the APOBEC enzyme. We hypothesised that the APOBEC enzyme, when fused with a Cas13 protein may perform a C to U conversion for a specific RNA target.

Hence, our project aims to develop and verify an RNA editing system using the enzyme APOBEC fused to dCas13b. Deactivated Cas13b, which differs from the activated Cas13b by two amino acids (H133A and H1058A), is able to still be guided by guide RNAs (gRNAs) to target the specific RNA strand. However, as enzymatic activity is deactivated, no cleavage of RNA strands will occur. dCas13b together with the gRNA will guide the fusion protein to the appropriate site on the target mRNA to be edited. Then, the APOBEC will make the specific C to U edit on the mRNA strand.

Before the fusion protein can be synthesised, a linker sequence is required between rAPOBEC and dCas13 to prevent misfolding of the two proteins. In addition, we attempted to model the expected 3D structure of the fusion protein. In Komor et al. (2016), several different linkers were tested to link rat APOBEC (rAPOBEC) and dCas9, and the XTEN linker sequence (SGSETPGTSESATPES) was shown to be the most efficient. Hence, XTEN was chosen as the linker sequence to link APOBEC and dCas13b for our fusion protein.

rAPOBEC-XTEN was extracted from the Base Editor 3 (BE3) plasmid (rAPOBEC1-XTEN-Cas9n-UGI-NLS, plasmid 73021) via PCR. dCas13b from Prevotella sp. P5-125 was extracted from the pC0049 plasmid as obtained from Addgene plasmid #103865. The gene fragments were cloned into px330A plasmid (Figure 2). We also designed (as elaborated in Section 3) and expressed our gRNA under the U6 promoter.

rAPOBEC-XTEN was extracted from the Base Editor 3 (BE3) plasmid (rAPOBEC1-XTEN-Cas9n-UGI-NLS, plasmid 73021) via PCR. dCas13b from Prevotella sp. P5-125 was extracted from the pC0049 plasmid as obtained from Addgene plasmid #103865. The gene fragments were cloned into px330A plasmid (Figure 2). We also designed (as elaborated in Section 3) and expressed our gRNA under the U6 promoter.

To design our gRNA sequences, we adopted the method that was described in Cox et al. (2017). According to the paper, the A-to-I base editing efficiency was most optimal when using the hairpin sequence of 5’ -GUUGUGGAAGGUCCAGUUUUGGGGGCUAUUACAACA- 3’ affixed to the 3’ end of the spacer domain. We also used a spacer length of 50 bp, with a mismatch position of around 10-30 bp as suggested in the paper. Such a design criterion has been shown to be successful in optimising successful gRNAs for RNA editing experiments. According to Sakuma et al. (2014), the terminator site is situated at the end of Cas9 hairpin motif site in px330A, thus our gRNA sequence will have to be synthesised with a U6 terminator sequence at the 3’ end to prevent the coding of an elongated hairpin domain.

Taking the above considerations into account, we wrote a PythonTM script to help us design and generate suitable gRNA gene blocks for synthesis. Firstly, the targeted mRNA sequence and its associated mutant site position will be defined by the user. The script will then perform a search for the mismatch base in the defined region and generate a spacer sequence that is reverse-complementary to the original strand. The hairpin motif with the U6 terminator sequence is thereafter concatenated to the 3’ end of the spacer sequence, before being reverse-transcribed to its cDNA form. Finally, BbsI restriction sites and junk sequences will be added to both 5’ and 3’ ends to obtain the gRNA gene block sequence (Figure 4).

To test our RNA editing system, we will first analyse the in vitro cleavage activity of our APOBEC enzyme using a deaminase assay. Subsequently, we will analyse our RNA editing system in vivo using cultured cells. To do that, we plan to express our dCas13b-APOBEC device (with gRNA) and our fluorescence reporter device in mammalian cells. We will be checking for the restoration of our green fluorescent protein (GFP) reporter by flow cytometry and fluorescence microscopy.

In addition, we also plan to test our system on its ability to edit mutated bases in our mammalian β-galactosidase enzyme. Point mutations in the β-galactosidase gene have been implicated in lysosomal storage disease and our RNA editing device could act as a potential therapeutic in the treatment of the disease.