Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates

The tumor suppressor p53 is a master regulator of cellular stress response pathways, including cell cycle arrest and apoptosis. Here, the authors identify molecular mechanisms of p53 binding to high- and low-affinity p53 response elements in the genome, linked to cell cycle arrest and pro-apoptotic...

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Autores principales: Marina Farkas, Hideharu Hashimoto, Yingtao Bi, Ramana V. Davuluri, Lois Resnick-Silverman, James J. Manfredi, Erik W. Debler, Steven B. McMahon
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3f1e9178c9564dfeb7beebe3db18db73
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spelling oai:doaj.org-article:3f1e9178c9564dfeb7beebe3db18db732021-12-02T13:57:04ZDistinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates10.1038/s41467-020-20783-z2041-1723https://doaj.org/article/3f1e9178c9564dfeb7beebe3db18db732021-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-20783-zhttps://doaj.org/toc/2041-1723The tumor suppressor p53 is a master regulator of cellular stress response pathways, including cell cycle arrest and apoptosis. Here, the authors identify molecular mechanisms of p53 binding to high- and low-affinity p53 response elements in the genome, linked to cell cycle arrest and pro-apoptotic genes, respectively.Marina FarkasHideharu HashimotoYingtao BiRamana V. DavuluriLois Resnick-SilvermanJames J. ManfrediErik W. DeblerSteven B. McMahonNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Marina Farkas
Hideharu Hashimoto
Yingtao Bi
Ramana V. Davuluri
Lois Resnick-Silverman
James J. Manfredi
Erik W. Debler
Steven B. McMahon
Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
description The tumor suppressor p53 is a master regulator of cellular stress response pathways, including cell cycle arrest and apoptosis. Here, the authors identify molecular mechanisms of p53 binding to high- and low-affinity p53 response elements in the genome, linked to cell cycle arrest and pro-apoptotic genes, respectively.
format article
author Marina Farkas
Hideharu Hashimoto
Yingtao Bi
Ramana V. Davuluri
Lois Resnick-Silverman
James J. Manfredi
Erik W. Debler
Steven B. McMahon
author_facet Marina Farkas
Hideharu Hashimoto
Yingtao Bi
Ramana V. Davuluri
Lois Resnick-Silverman
James J. Manfredi
Erik W. Debler
Steven B. McMahon
author_sort Marina Farkas
title Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
title_short Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
title_full Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
title_fullStr Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
title_full_unstemmed Distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
title_sort distinct mechanisms control genome recognition by p53 at its target genes linked to different cell fates
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3f1e9178c9564dfeb7beebe3db18db73
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