DAF-16/FOXO and HLH-30/TFEB function as combinatorial transcription factors to promote stress resistance and longevity
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- dc.contributor.author Lin, Xin-Xuan
- dc.contributor.author Sen, Ilke
- dc.contributor.author Janssens, Georges E.
- dc.contributor.author Zhou, Xin
- dc.contributor.author Fonslow, Bryan R.
- dc.contributor.author Edgar, Daniel
- dc.contributor.author Stroustrup, Nicholas
- dc.contributor.author Swoboda, Peter
- dc.contributor.author Yates, John R.
- dc.contributor.author Ruvkun, Gary
- dc.contributor.author Riedel, Christian G.
- dc.date.accessioned 2019-11-25T08:32:19Z
- dc.date.available 2019-11-25T08:32:19Z
- dc.date.issued 2018
- dc.description.abstract The ability to perceive and respond to harmful conditions is crucial for the survival of any organism. The transcription factor DAF-16/FOXO is central to these responses, relaying distress signals into the expression of stress resistance and longevity promoting genes. However, its sufficiency in fulfilling this complex task has remained unclear. Using C. elegans, we show that DAF-16 does not function alone but as part of a transcriptional regulatory module, together with the transcription factor HLH-30/TFEB. Under harmful conditions, both transcription factors translocate into the nucleus, where they often form a complex, co-occupy target promoters, and co-regulate many target genes. Interestingly though, their synergy is stimulus-dependent: They rely on each other, functioning in the same pathway, to promote longevity or resistance to oxidative stress, but they elicit heat stress responses independently, and they even oppose each other during dauer formation. We propose that this module of DAF-16 and HLH-30 acts by combinatorial gene regulation to relay distress signals into the expression of specific target gene sets, ensuring optimal survival under each given threat.
- dc.format.mimetype application/pdf
- dc.identifier.citation Lin XX, Sen I, Janssens GE, Zhou X, Fonslow BR, Edgar D et al. DAF-16/FOXO and HLH-30/TFEB function as combinatorial transcription factors to promote stress resistance and longevity. Nat Commun. 2018;9(1):4400. DOI: 10.1038/s41467-018-06624-0
- dc.identifier.doi http://dx.doi.org/10.1038/s41467-018-06624-0
- dc.identifier.issn 2041-1723
- dc.identifier.uri http://hdl.handle.net/10230/42954
- dc.language.iso eng
- dc.publisher Nature Research
- dc.relation.ispartof Nature Communications. 2018;9(1):4400
- dc.rights © The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
- dc.rights.accessRights info:eu-repo/semantics/openAccess
- dc.rights.uri http://creativecommons.org/licenses/by/4.0/
- dc.subject.keyword Ageing
- dc.subject.keyword Gene expression
- dc.subject.keyword Transcription
- dc.title DAF-16/FOXO and HLH-30/TFEB function as combinatorial transcription factors to promote stress resistance and longevity
- dc.type info:eu-repo/semantics/article
- dc.type.version info:eu-repo/semantics/publishedVersion