z-logo
open-access-imgOpen Access
Highly efficient Cas9-mediated transcriptional programming
Author(s) -
Alejandro Chavez,
Jonathan Scheiman,
Suhani Vora,
Benjamin W. Pruitt,
Marcelle Tuttle,
Eswar Prasad R. Iyer,
Shuailiang Lin,
Samira Kiani,
Christopher D. Guzman,
Daniel J. Wiegand,
Dmitry TerOvanesyan,
Jonathan L. Braff,
Noah Davidsohn,
Benjamin E. Housden,
Norbert Perrimon,
Ron Weiss,
John Aach,
James J. Collins,
George M. Church
Publication year - 2015
Publication title -
nature methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.469
H-Index - 318
eISSN - 1548-7105
pISSN - 1548-7091
DOI - 10.1038/nmeth.3312
Subject(s) - cas9 , nuclease , biology , activator (genetics) , induced pluripotent stem cell , gene , microbiology and biotechnology , regulator , transcription factor , crispr , computational biology , embryonic stem cell , genetics
The RNA-guided nuclease Cas9 can be reengineered as a programmable transcription factor. However, modest levels of gene activation have limited potential applications. We describe an improved transcriptional regulator obtained through the rational design of a tripartite activator, VP64-p65-Rta (VPR), fused to nuclease-null Cas9. We demonstrate its utility in activating endogenous coding and noncoding genes, targeting several genes simultaneously and stimulating neuronal differentiation of human induced pluripotent stem cells (iPSCs).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom