Applications of Cas9 as an RNA-programmed RNA-binding protein

被引:31
|
作者
Nelles, David A. [1 ,2 ]
Fang, Mark Y. [1 ,2 ]
Aigner, Stefan [1 ,2 ]
Yeo, Gene W. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif San Diego, Stem Cell Program, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
[3] Natl Univ Singapore, Mol Engn Lab, Inst Biomed Sci, Agcy Sci Technol & Res, Singapore 117548, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore 117595, Singapore
关键词
Cas9; CRISPR-Cas; RCas9; RNA-binding proteins; RNA biology; RNA targeting; HEXANUCLEOTIDE REPEAT; EXPRESSION; CRISPR; LOCALIZATION; DYNAMICS; VISUALIZATION; RECOGNITION; CLEAVAGE; REVEALS; DOMAINS;
D O I
10.1002/bies.201500001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Streptococcus pyogenes CRISPR-Cas system has gained widespread application as a genome editing and gene regulation tool as simultaneous cellular delivery of the Cas9 protein and guide RNA senables recognition of specific DNA sequences. The recent discovery that Cas9 can also bind and cleave RNA in an RNA-programmable manner indicates the potential utility of this system as a universal nucleic acid-recognition technology. RNA-targeted Cas9 (RCas9) could allow identification and manipulation of RNA substrates in live cells, empowering the study of cellular gene expression, and could ultimately spawn patient-and disease-specific diagnostic and therapeutic tools. Here we describe the development of RCas9 and compare it to previous methods for RNA targeting, including engineered RNA-binding proteins and other types of CRISPR-Cas systems. We discuss potential uses ranging from live imaging of transcriptional dynamics to patient-specific therapies and applications in synthetic biology.
引用
收藏
页码:732 / 739
页数:8
相关论文
共 50 条
  • [1] High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity
    Pattanayak, Vikram
    Lin, Steven
    Guilinger, John P.
    Ma, Enbo
    Doudna, Jennifer A.
    Liu, David R.
    NATURE BIOTECHNOLOGY, 2013, 31 (09) : 839 - +
  • [2] High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity
    Vikram Pattanayak
    Steven Lin
    John P Guilinger
    Enbo Ma
    Jennifer A Doudna
    David R Liu
    Nature Biotechnology, 2013, 31 : 839 - 843
  • [3] Cleaving RNA with Cas9
    Ghodsizadeh, Odelia
    NATURE METHODS, 2014, 11 (11) : 1090 - 1090
  • [4] RNA targeting by Cas9
    Eytan Zlotorynski
    Nature Reviews Molecular Cell Biology, 2014, 15 (11) : 701 - 701
  • [5] Cleaving RNA with Cas9
    Odelia Ghodsizadeh
    Nature Methods, 2014, 11 : 1090 - 1090
  • [6] Design of RNA-Binding Oligopeptides Based on Information of RNA-Binding Protein
    Naohiko Shimada
    Reiko Iwase
    Tetsuji Yamaoka
    Akira Murakami
    Polymer Journal, 2003, 35 : 507 - 512
  • [7] Design of RNA-binding oligopeptides based on information of RNA-binding protein
    Shimada, N
    Iwase, R
    Yamaoka, T
    Murakami, A
    POLYMER JOURNAL, 2003, 35 (06) : 507 - 512
  • [8] RNA-binding protein kinetics
    Arunima Singh
    Nature Methods, 2021, 18 : 335 - 335
  • [9] RNA-binding protein kinetics
    Singh, Arunima
    NATURE METHODS, 2021, 18 (04) : 335 - 335
  • [10] RNA-programmed genome editing in human cells
    Jinek, Martin
    East, Alexandra
    Cheng, Aaron
    Lin, Steven
    Ma, Enbo
    Doudna, Jennifer
    ELIFE, 2013, 2