Simultaneous repression of multiple bacterial genes using nonrepetitive extra-long sgRNA arrays-Reference-Cited by-同舟云学术

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Simultaneous repression of multiple bacterial genes using nonrepetitive extra-long sgRNA arrays

Published:2019-10-07 Issue:11 Volume:37 Page:1294-1301
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Reis Alexander C.,Halper Sean M.,Vezeau Grace E.,Cetnar Daniel P.,Hossain Ayaan^ORCID,Clauer Phillip R.,Salis Howard M.^ORCID

Funder

U.S. Department of Energy

United States Department of Defense | Defense Advanced Research Projects Agency

National Science Foundation

United States Department of Defense | United States Air Force | AFMC | Air Force Office of Scientific Research

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://www.nature.com/articles/s41587-019-0286-9.pdf

Reference49 articles.

1. Dominguez, A. A., Lim, W. A. & Qi, L. S. Beyond editing: repurposing CRISPR–Cas9 for precision genome regulation and interrogation. Nat. Rev. Mol. Cell Biol. 17, 5–15 (2016).

2. Barrangou, R. & Horvath, P. A decade of discovery: CRISPR functions and applications. Nat. Microbiol. 2, 17092 (2017).

3. Halperin, S. O. et al. CRISPR-guided DNA polymerases enable diversification of all nucleotides in a tunable window. Nature 560, 248–252 (2018).

4. Peters, J. M. et al. Enabling genetic analysis of diverse bacteria with Mobile-CRISPRi. Nat. Microbiol. 4, 244–250 (2019).

5. Komor, A. C., Kim, Y. B., Packer, M. S., Zuris, J. A. & Liu, D. R. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage. Nature 533, 420–424 (2016).

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