Harnessing non-Watson-Crick's base pairing to enhance CRISPR effectors cleavage activities and enable gene editing in mammalian cells.
CRISPR
Cas12a
Cas9
RNA
genetic alphabet
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
09 Jan 2024
09 Jan 2024
Historique:
medline:
27
12
2023
pubmed:
27
12
2023
entrez:
27
12
2023
Statut:
ppublish
Résumé
Genomic DNA of the cyanophage S-2L virus is composed of 2-aminoadenine (Z), thymine (T), guanine (G), and cytosine (C), forming the genetic alphabet ZTGC, which violates Watson-Crick base pairing rules. The Z-base has an extra amino group on the two position that allows the formation of a third hydrogen bond with thymine in DNA strands. Here, we explored and expanded applications of this non-Watson-Crick base pairing in protein expression and gene editing. Both ZTGC-DNA (Z-DNA) and ZUGC-RNA (Z-RNA) produced in vitro show detectable compatibility and can be decoded in mammalian cells, including
Identifiants
pubmed: 38150477
doi: 10.1073/pnas.2308415120
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2308415120Déclaration de conflit d'intérêts
Competing interests statement:Q.X. and S.G. are inventors of a pending patent related to this work filed by Tufts University. Q.X. is the founder and has equity in Hopewell Therapeutics Inc.