| Literature DB >> 33654892 |
Yu Jia1, Da Shen1, Xia Wang1, Jin Sun1, Ping Peng1, Rong-Gang Xu1, Bowen Xu1, Jian-Quan Ni1,2.
Abstract
Powerful and general methods that can enhance gene expression are useful to systematically study gene function. To date, compared with the methods in generating loss-of-function mutants, methods to achieve gain-of-function are limited. The entire field in Drosophila has relied heavily on the Gal4/UAS:cDNA overexpression system developed over two decades ago. It is laborious and expensive to clone the coding DNA sequence (CDS) of a gene, especially those of large size. In addition, side effects of this method are often observed because of the ectopic expression. Also, simultaneous activation of two genes with the traditional method is often time-consuming, and few are achievable for three or more genes. In this protocol, we describe how to build an effective and convenient targeting activator system, flySAM, to activate endogenous genes in Drosophila melanogaster based on the structure-guided engineering of CRISPR-Cas9 complex.Entities:
Keywords: CRISPR-Cas nuclease; CRISPRa; Drosophila; dCas9; flySAM
Year: 2019 PMID: 33654892 PMCID: PMC7854103 DOI: 10.21769/BioProtoc.3147
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325