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1. A protein with an unusually short PPR domain, MEF8, affects editing at over 60 Arabidopsis mitochondrial C targets of RNA editing

   https://doi.org/10.1111/tpj.13709  

   Diaz, Michael F. ; Bentolila, Stephane ; Hayes, Michael L. ; Hanson, Maureen R. ; Mulligan, R. Michael ( November 2017 , The Plant Journal)
2. RNA-editing enzymes ADAR1 and ADAR2 coordinately regulate the editing and expression of Ctn RNA

   https://doi.org/10.1002/1873-3468.12795  

   Anantharaman, Aparna ; Gholamalamdari, Omid ; Khan, Abid ; Yoon, Je-Hyun ; Jantsch, Michael F. ; Hartner, Jochen C. ; Gorospe, Myriam ; Prasanth, Supriya G. ; Prasanth, Kannanganattu V. ( September 2017 , FEBS Letters)
3. Genome Editing with CRISPR‐Cas9 in Lactobacillus plantarum Revealed That Editing Outcomes Can Vary Across Strains and Between Methods

   https://doi.org/10.1002/biot.201700583  

   Leenay, Ryan T. ; Vento, Justin M. ; Shah, Malay ; Martino, Maria Elena ; Leulier, François ; Beisel, Chase L. ( September 2018 , Biotechnology Journal)
4. Targeted editing and evolution of engineered ribosomes in vivo by filtered editing

   https://doi.org/10.1038/s41467-021-27836-x  

   Radford, Felix ; Elliott, Shane D. ; Schepartz, Alanna ; Isaacs, Farren J. ( January 2022 , Nature Communications)

   Genome editing technologies introduce targeted chromosomal modifications in organisms yet are constrained by the inability to selectively modify repetitive genetic elements. Here we describe filtered editing, a genome editing method that embeds group 1 self-splicing introns into repetitive genetic elements to construct unique genetic addresses that can be selectively modified. We introduce intron-containing ribosomes into theE. coligenome and perform targeted modifications of these ribosomes using CRISPR/Cas9 and multiplex automated genome engineering. Self-splicing of introns post-transcription yields scarless RNA molecules, generating a complex library of targeted combinatorial variants. We use filtered editing to co-evolve the 16S rRNA to tune the ribosome’s translational efficiency and the 23S rRNA to isolate antibiotic-resistant ribosome variants without interfering with native translation. This work sets the stage to engineer mutant ribosomes that polymerize abiological monomers with diverse chemistries and expands the scope of genome engineering for precise editing and evolution of repetitive DNA sequences.
5. Editing Domain Motions Preorganize the Synthetic Active Site of Prolyl-tRNA Synthetase

   https://doi.org/10.1021/acscatal.0c02381  

   Hu, Quin H. ; Williams, Murphi T. ; Shulgina, Irina ; Fossum, Carl J. ; Weeks, Katelyn M. ; Adams, Lauren M. ; Reinhardt, Clorice R. ; Musier-Forsyth, Karin ; Hati, Sanchita ; Bhattacharyya, Sudeep ( September 2020 , ACS Catalysis)