Transcript-Specific Site-Directed RNA Editing Reveals Principles for Splice-aware guide RNA Design
Schneider, N.; Zehoray, N.; Steinberg, R.; Banin, E.; Arsenijevic, Y.; Ben Aroya, S.; Levanon, E. Y.; Sharon, D.
Show abstract
Site-directed RNA editing (SDRE) utilizing the adenosine deaminase acting on RNA (ADAR) enzymes is commonly facilitated by guide RNAs (gRNAs) optimized to enhance on-target editing and minimize bystander effects. However, the impact of gRNA binding and ADAR-mediated SDRE on canonical pre-mRNA splicing remains poorly understood. Here, we developed an in vitro transcript-specific editing strategy that enables selective targeting and direct comparison of SDRE in pre-mRNA and mature mRNA. Using splice-relevant variants associated with inherited retinal diseases, we investigated the effects of SDRE on exonic, near-canonical intronic, and deep intronic splice variants. We identified gRNA-induced splice perturbation at exonic and intronic targets and observed that higher editing levels could be associated with increased splice disruption. Conversely, SDRE of two exonic splice variants and a deep intronic variant resulted in increased production of correctly spliced transcripts, demonstrating the potential of SDRE for splice modulation. Finally, by dissecting the effects of ADAR expression and gRNA design on editing and splicing outcomes, we established a system for identifying design principles that reduce splice interference and enhance the generation of correctly spliced, edited transcripts. These findings highlight the importance of considering transcript context and splicing consequences in the development of SDRE-based therapeutic strategies. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=92 SRC="FIGDIR/small/741163v1_ufig1.gif" ALT="Figure 1"> View larger version (28K): org.highwire.dtl.DTLVardef@2e4703org.highwire.dtl.DTLVardef@3834d3org.highwire.dtl.DTLVardef@1409c8org.highwire.dtl.DTLVardef@18e463b_HPS_FORMAT_FIGEXP M_FIG Created in BioRender. Schneider, N. (2026) https://BioRender.com/59i0tiy C_FIG
Matching journals
The top 1 journal accounts for 50% of the predicted probability mass.
Similar papers in this journal
- A CRISPR-dCas13 RNA-editing tool to study alternative splicing 97%
- Structural disruption of exonic stem-loops immediately upstream of the intron regulates mammalian splicing 97%
- Exon junction complex-associated multi-adapter RNPS1 nucleates splicing regulatory complexes to maintain transcriptome surveillance 96%
Similar papers in this journal
- OpenASO: RNA Rescue--designing splice-modulating antisense oligonucleotides through community science 94%
- APOBEC1 mediated C-to-U RNA editing: target sequence and trans-acting factor contribution to 177 RNA editing events in 119 murine transcripts in-vivo 94%
- Global Analysis by LC-MS/MS of N6-Methyladenosine and Inosine in mRNA Reveals Complex Incidence 93%
Similar papers in this journal
- CRISPR-Cas9 cytidine and adenosine base editing of splice-sites mediates highly-efficient disruption of proteins in primary cells 95%
- Dissecting the basis for differential substrate specificity of ADAR1 and ADAR2 95%
- Expanded palette of RNA base editors for comprehensive RBP-RNA interactome studies 95%
Similar papers in this journal
- Single-stranded HDR templates with truncated Cas12a binding sequences improve knock-in efficiencies in primary human T cells 92%
- shRNAI: a deep neural network for the design of highly potent shRNAs 92%
- Seed-Mediated RNA Interference Of Androgen Signaling And Survival Networks Induces Cell Death In Prostate Cancer Cells 91%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.