The budding yeast Start repressor Whi7 differs in regulation from Whi5, emerging as a major cell cycle brake in response to stress

Autor: Ester Méndez, Manuel Mendoza, Mercè Gomar-Alba, J. Carlos Igual, M. Carmen Bañó, Inma Quilis
Přispěvatelé: Universitat de València (UV), Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA), Mendoza, Manuel, Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Journal of Cell Science
Journal of Cell Science, Company of Biologists, 2020, 133 (24), ⟨10.1242/jcs.251413⟩
Journal of Cell Science, 2020, 133 (24), ⟨10.1242/jcs.251413⟩
Méndez Belinchón, Ester Gomar Alba, Mercè Bañó Aracil, María del Carmen Mendoza, Manuel Quilis Bayarri, Inmaculada Igual García, Juan Carlos 2020 The budding yeast Start repressor Whi7 differs in regulation from Whi5, emerging as a major cell cycle brake in response to stress Journal of Cell Science 133 24
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
RODERIC: Repositorio Institucional de la Universitat de Valéncia
article-version (VoR) Version of Record
ISSN: 0021-9533
1477-9137
DOI: 10.1242/jcs.251413⟩
Popis: Start is the main decision point in the eukaryotic cell cycle at which cells commit to a new round of cell division. It involves the irreversible activation of a transcriptional programme through the inactivation of Start transcriptional repressors: the retinoblastoma family in mammals, or Whi5 and its recently identified paralogue Whi7 (also known as Srl3) in budding yeast. Here, we provide a comprehensive comparison of Whi5 and Whi7 that reveals significant qualitative differences. Indeed, the expression, subcellular localization and functionality of Whi7 and Whi5 are differentially regulated. Importantly, Whi7 shows specific properties in its association with promoters not shared by Whi5, and for the first time, we demonstrate that Whi7, and not Whi5, can be the main contributor to Start inhibition such as it occurs in the response to cell wall stress. Our results help to improve understanding of the interplay between multiple differentially regulated Start repressors in order to face specific cellular conditions.
Highlighted Article: Cells can use the interplay between functionally redundant but differentially regulated cell-cycle repressors in order to confer new repression capabilities and to respond to specific cellular conditions.
Databáze: OpenAIRE