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Cited by 316

The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.

Multiplexable, locus-specific targeting of long RNAs with CRISPR-Display

Open access
Shechner, David M, Hacisuleyman, Ezgi, Younger, Scott T, Rinn, John L·2015·Nature Methods

Abstract

Noncoding RNAs play diverse roles throughout biology and exhibit broad functional capacity. To investigate and harness these capabilities, we developed clustered regularly interspaced short palindromic repeats (CRISPR)-Display (CRISP-Disp), a targeted localization method that uses Cas9 to deploy large RNA cargos to DNA loci. We demonstrate that functional RNA domains up to at least 4.8 kb long can be inserted in CRISPR guide RNA at multiple points, allowing the construction of Cas9 complexes with protein-binding cassettes, artificial aptamers, pools of random sequences and natural long noncoding RNAs. A unique feature of CRISP-Disp is the multiplexing of distinct functions at multiple targets, limited only by the availability of functional RNA motifs. We anticipate the use of CRISP-Disp for ectopically targeting functional RNAs and ribonucleoprotein (RNP) complexes to genomic loci.

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Crossref · 10.1038/nmeth.3433

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Metadata

Authors
Shechner, D. M., Hacisuleyman, E., Younger, S. T., & Rinn, J. L.
Venue
Nature Methods
Published
2015-06-01
Volume
12
Issue
7
Pages
664-670
ISSN
  • 1548-7091 (ISSN-L)
  • 1548-7105
OpenAlex
W1505917984
Cited by
316
References
8
FWCI
15.82
Type
journal article
Language
en
Open access
green

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