| Literature DB >> 31704182 |
Stephen S Gisselbrecht1, Alexandre Palagi2, Jesse V Kurland1, Julia M Rogers3, Hakan Ozadam4, Ye Zhan4, Job Dekker5, Martha L Bulyk6.
Abstract
A major challenge in biology is to understand how complex gene expression patterns are encoded in the genome. While transcriptional enhancers have been studied extensively, few transcriptional silencers have been identified, and they remain poorly understood. Here, we used a novel strategy to screen hundreds of sequences for tissue-specific silencer activity in whole Drosophila embryos. Almost all of the transcriptional silencers that we identified were also active enhancers in other cellular contexts. These elements are bound by more transcription factors than non-silencers. A subset of these silencers forms long-range contacts with promoters. Deletion of a silencer caused derepression of its target gene. Our results challenge the common practice of treating enhancers and silencers as separate classes of regulatory elements and suggest the possibility that thousands or more bifunctional CRMs remain to be discovered in Drosophila and 104-105 in humans.Entities:
Keywords: cis-regulatory elements; enhancers; promoter looping; repression; silencers; transcriptional regulation
Mesh:
Year: 2019 PMID: 31704182 PMCID: PMC6980774 DOI: 10.1016/j.molcel.2019.10.004
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970