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TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac...

TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3fc4fb45806142b6abbf012e462c3364

TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac aging

About this item

Full title

TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac aging

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2018-07, Vol.9 (1), p.2560-13, Article 2560

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Cellular senescence is a well-orchestrated programmed process involved in age-related pathologies, tumor suppression and embryonic development. TGF-β/Smad is one of the predominant pathways that regulate damage-induced and developmentally programmed senescence. Here we show that canonical TGF-β signaling promotes senescence via miR-29-induced loss...

Alternative Titles

Full title

TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac aging

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3fc4fb45806142b6abbf012e462c3364

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3fc4fb45806142b6abbf012e462c3364

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-018-04994-z

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