| Literature DB >> 32142631 |
Shannon E Keenan1, Shelby A Blythe2, Robert A Marmion3, Nareg J-V Djabrayan3, Eric F Wieschaus4, Stanislav Y Shvartsman5.
Abstract
Optogenetic perturbations, live imaging, and time-resolved ChIP-seq assays in Drosophila embryos were used to dissect the ERK-dependent control of the HMG-box repressor Capicua (Cic), which plays critical roles in development and is deregulated in human spinocerebellar ataxia and cancers. We established that Cic target genes are activated before significant downregulation of nuclear localization of Cic and demonstrated that their activation is preceded by fast dissociation of Cic from the regulatory DNA. We discovered that both Cic-DNA binding and repression are rapidly reinstated in the absence of ERK activation, revealing that inductive signaling must be sufficiently sustained to ensure robust transcriptional response. Our work provides a quantitative framework for the mechanistic analysis of dynamics and control of transcriptional repression in development. Published by Elsevier Inc.Entities:
Keywords: Capicua; Drosophila; ERK; cellular signaling; development; optogenetics; transcriptional repression
Mesh:
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Year: 2020 PMID: 32142631 PMCID: PMC7161736 DOI: 10.1016/j.devcel.2020.02.004
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270