Express or repress? The transcriptional dilemma of damaged chromatin

被引:30
作者
Capozzo, Ilaria [1 ,2 ]
Iannelli, Fabio [3 ]
Francia, Sofia [1 ,3 ]
di Fagagna, Fabrizio d'Adda [1 ,3 ]
机构
[1] CNR, Ist Genet Mol, I-27100 Pavia, Italy
[2] Scuola Univ Super IUSS Pavia, Pavia, Italy
[3] FIRC Inst Mol Oncol Fdn, IFOM Fdn, I-20139 Milan, Italy
基金
欧洲研究理事会;
关键词
chromatin; DNA damage response; DNA double-strand breaks; gene silencing; noncoding RNAs; RNA Polymerase II; transcription; DOUBLE-STRAND BREAK; HOMOLOGY-DIRECTED REPAIR; DNA-DAMAGE; HUMAN-CELLS; SMALL RNAS; CHROMOSOME BREAKS; CELLULAR-RESPONSE; GENOME REGULATION; OXIDATIVE DAMAGE; NONCODING RNAS;
D O I
10.1111/febs.14048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The fine modulation of transcriptional activity around DNA lesions is essential to carefully regulate the crosstalk between the activation of the DNA damage response, DNA repair and transcription, particularly when the lesion occurs next to actively transcribed genes. Recently, several studies have been carried out to investigate how DNA lesions impact on local transcription, but the emerging model remains incomplete. Transcription of genes around damaged DNA is actively downregulated by the DNA damage response through different mechanisms, which appear specific to the chromatin context, the type of DNA damage or its complexity. Intriguingly, emerging evidence also indicates that transcription of noncoding RNAs (ncRNAs) is induced at sites of DNA damage, producing small ncRNAs that are, in turn, required for a full DNA damage response activation. We discuss here these recent findings, highlighting the major unresolved questions in the field, and propose ways to reconcile these apparently contradictory observations.
引用
收藏
页码:2133 / 2147
页数:15
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