Precise integration of inducible transcriptional elements (PrIITE) enables absolute control of gene expression
Author(s) -
Rita Pinto,
Lars Hestbjerg Hansen,
John Hintze,
Raquel Almeida,
Sylvester Larsen,
Mehmet Coskun,
Johanne Davidsen,
Cathy Mitchelmore,
Leonor David,
Jesper T. Troelsen,
Eric Bennett
Publication year - 2017
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkx371
Subject(s) - biology , effector , gene , reporter gene , gene expression , regulation of gene expression , computational biology , transcription factor , genetics , genome editing , exon , endogeny , microbiology and biotechnology , genome , endocrinology
Tetracycline-based inducible systems provide powerful methods for functional studies where gene expression can be controlled. However, the lack of tight control of the inducible system, leading to leakiness and adverse effects caused by undesirable tetracycline dosage requirements, has proven to be a limitation. Here, we report that the combined use of genome editing tools and last generation Tet-On systems can resolve these issues. Our principle is based on precise integration of inducible transcriptional elements (coined PrIITE) targeted to: (i) exons of an endogenous gene of interest (GOI) and (ii) a safe harbor locus. Using PrIITE cells harboring a GFP reporter or CDX2 transcription factor, we demonstrate discrete inducibility of gene expression with complete abrogation of leakiness. CDX2 PrIITE cells generated by this approach uncovered novel CDX2 downstream effector genes. Our results provide a strategy for characterization of dose-dependent effector functions of essential genes that require absence of endogenous gene expression.
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