miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage

MiR-34 is a tumour suppressor microRNA known to be upregulated by p53 after DNA damage and plays a critical role in cell cycle arrest and apoptosis. Here the authors show the cell maintains an inactive pool of miR-34 which is rapidly activated after damage via ATM-dependent phosphorylation.

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Autores principales: David W. Salzman, Kotoka Nakamura, Sunitha Nallur, Michelle T. Dookwah, Chanatip Metheetrairut, Frank J. Slack, Joanne B. Weidhaas
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/1a9e7f7933464a6e8a6b14db680cf5b9
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spelling oai:doaj.org-article:1a9e7f7933464a6e8a6b14db680cf5b92021-12-02T15:35:22ZmiR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage10.1038/ncomms109542041-1723https://doaj.org/article/1a9e7f7933464a6e8a6b14db680cf5b92016-03-01T00:00:00Zhttps://doi.org/10.1038/ncomms10954https://doaj.org/toc/2041-1723MiR-34 is a tumour suppressor microRNA known to be upregulated by p53 after DNA damage and plays a critical role in cell cycle arrest and apoptosis. Here the authors show the cell maintains an inactive pool of miR-34 which is rapidly activated after damage via ATM-dependent phosphorylation.David W. SalzmanKotoka NakamuraSunitha NallurMichelle T. DookwahChanatip MetheetrairutFrank J. SlackJoanne B. WeidhaasNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
David W. Salzman
Kotoka Nakamura
Sunitha Nallur
Michelle T. Dookwah
Chanatip Metheetrairut
Frank J. Slack
Joanne B. Weidhaas
miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage
description MiR-34 is a tumour suppressor microRNA known to be upregulated by p53 after DNA damage and plays a critical role in cell cycle arrest and apoptosis. Here the authors show the cell maintains an inactive pool of miR-34 which is rapidly activated after damage via ATM-dependent phosphorylation.
format article
author David W. Salzman
Kotoka Nakamura
Sunitha Nallur
Michelle T. Dookwah
Chanatip Metheetrairut
Frank J. Slack
Joanne B. Weidhaas
author_facet David W. Salzman
Kotoka Nakamura
Sunitha Nallur
Michelle T. Dookwah
Chanatip Metheetrairut
Frank J. Slack
Joanne B. Weidhaas
author_sort David W. Salzman
title miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage
title_short miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage
title_full miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage
title_fullStr miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage
title_full_unstemmed miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage
title_sort mir-34 activity is modulated through 5′-end phosphorylation in response to dna damage
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/1a9e7f7933464a6e8a6b14db680cf5b9
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