Blurring the line between the DNA damage response and transcription: The importance of chromatin dynamics

DNA damage interferes with the progression of transcription machineries. A tight coordination of transcription with signaling and repair of DNA damage is thus critical for safeguarding genome function. This coordination involves modulations of chromatin organization. Here, we focus on the central ro...

Full description

Saved in:
Bibliographic Details
Published inExperimental cell research Vol. 329; no. 1; pp. 148 - 153
Main Authors Adam, Salomé, Polo, Sophie E.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.11.2014
Elsevier BV
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:DNA damage interferes with the progression of transcription machineries. A tight coordination of transcription with signaling and repair of DNA damage is thus critical for safeguarding genome function. This coordination involves modulations of chromatin organization. Here, we focus on the central role of chromatin dynamics, in conjunction with DNA Damage Response (DDR) factors, in controlling transcription inhibition and restart at sites of DNA damage in mammalian cells. Recent work has identified chromatin modifiers and histone chaperones as key regulators of transcriptional activity in damaged chromatin regions. Conversely, the transcriptional state of chromatin before DNA damage influences both DNA damage signaling and repair. We discuss the importance of chromatin plasticity in coordinating the interplay between the DDR and transcription, with major implications for cell fate maintenance. •DNA damage signaling and repair regulate transcription of damaged chromatin.•Chromatin dynamics control transcription inhibition and recovery in damaged regions.•Chromatin transcriptional state influences DNA damage signaling and repair.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
ObjectType-Feature-3
ObjectType-Review-1
ISSN:0014-4827
1090-2422
DOI:10.1016/j.yexcr.2014.07.017