Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts

During S phase of the cell cycle, transcription and replication need to be coordinated in order to avoid conflicts leading to potential genomic instability. Here, the authors find that Mrc1 integrates signals from different kinases to regulate replication during unscheduled transcription events.

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Autores principales: Alba Duch, Berta Canal, Sonia I. Barroso, María García-Rubio, Gerhard Seisenbacher, Andrés Aguilera, Eulàlia de Nadal, Francesc Posas
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/890cd55d01074eb4acae28ff6220fd5b
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spelling oai:doaj.org-article:890cd55d01074eb4acae28ff6220fd5b2021-12-02T15:34:36ZMultiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts10.1038/s41467-017-02756-x2041-1723https://doaj.org/article/890cd55d01074eb4acae28ff6220fd5b2018-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-02756-xhttps://doaj.org/toc/2041-1723During S phase of the cell cycle, transcription and replication need to be coordinated in order to avoid conflicts leading to potential genomic instability. Here, the authors find that Mrc1 integrates signals from different kinases to regulate replication during unscheduled transcription events.Alba DuchBerta CanalSonia I. BarrosoMaría García-RubioGerhard SeisenbacherAndrés AguileraEulàlia de NadalFrancesc PosasNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Alba Duch
Berta Canal
Sonia I. Barroso
María García-Rubio
Gerhard Seisenbacher
Andrés Aguilera
Eulàlia de Nadal
Francesc Posas
Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts
description During S phase of the cell cycle, transcription and replication need to be coordinated in order to avoid conflicts leading to potential genomic instability. Here, the authors find that Mrc1 integrates signals from different kinases to regulate replication during unscheduled transcription events.
format article
author Alba Duch
Berta Canal
Sonia I. Barroso
María García-Rubio
Gerhard Seisenbacher
Andrés Aguilera
Eulàlia de Nadal
Francesc Posas
author_facet Alba Duch
Berta Canal
Sonia I. Barroso
María García-Rubio
Gerhard Seisenbacher
Andrés Aguilera
Eulàlia de Nadal
Francesc Posas
author_sort Alba Duch
title Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts
title_short Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts
title_full Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts
title_fullStr Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts
title_full_unstemmed Multiple signaling kinases target Mrc1 to prevent genomic instability triggered by transcription-replication conflicts
title_sort multiple signaling kinases target mrc1 to prevent genomic instability triggered by transcription-replication conflicts
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/890cd55d01074eb4acae28ff6220fd5b
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