Heat shock factor 1 promotes TERRA transcription and telomere protection upon heat stress

In response to metabolic or environmental stress, cells activate powerful defense mechanisms to prevent the formation and accumulation of toxic protein aggregates. The main orchestrator of this cellular response is HSF1 (heat shock factor 1), a transcription factor involved in the up-regulation of p...

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Published inNucleic acids research Vol. 45; no. 11; pp. 6321 - 6333
Main Authors Koskas, Sivan, Decottignies, Anabelle, Dufour, Solenne, Pezet, Mylène, Verdel, André, Vourc'h, Claire, Faure, Virginie
Format Journal Article
LanguageEnglish
Published England Oxford University Press 20.06.2017
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Summary:In response to metabolic or environmental stress, cells activate powerful defense mechanisms to prevent the formation and accumulation of toxic protein aggregates. The main orchestrator of this cellular response is HSF1 (heat shock factor 1), a transcription factor involved in the up-regulation of protein-coding genes with protective roles. It has become very clear that HSF1 has a broader function than initially expected. Indeed, our previous work demonstrated that, upon stress, HSF1 activates the transcription of a non-coding RNA, named Satellite III, at pericentromeric heterochromatin. Here, we observe that the function of HSF1 extends to telomeres and identify subtelomeric DNA as a new genomic target of HSF1. We show that the binding of HSF1 to subtelomeric regions plays an essential role in the upregulation of non-coding TElomeric Repeat containing RNA (TERRA) transcription upon heat shock. Importantly, our data show that telomere integrity is impacted by heat shock and that telomeric DNA damages are markedly enhanced in HSF1 deficient cells. Altogether, our findings reveal a new direct and essential function of HSF1 in the transcriptional activation of TERRA and in telomere protection upon stress.
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PMCID: PMC5499866
ISSN:0305-1048
1362-4962
DOI:10.1093/nar/gkx208