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Cryptochromes modulate E2F family transcription factors

Early 2 factor (E2F) family transcription factors participate in myriad cell biological processes including: the cell cycle, DNA repair, apoptosis, development, differentiation, and metabolism. Circadian rhythms influence many of these phenomena. Here we find that a mammalian circadian rhythm compon...

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Detalles Bibliográficos
Autores principales: Chan, Alanna B., Huber, Anne-Laure, Lamia, Katja A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058038/
https://www.ncbi.nlm.nih.gov/pubmed/32139766
http://dx.doi.org/10.1038/s41598-020-61087-y
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author Chan, Alanna B.
Huber, Anne-Laure
Lamia, Katja A.
author_facet Chan, Alanna B.
Huber, Anne-Laure
Lamia, Katja A.
author_sort Chan, Alanna B.
collection PubMed
description Early 2 factor (E2F) family transcription factors participate in myriad cell biological processes including: the cell cycle, DNA repair, apoptosis, development, differentiation, and metabolism. Circadian rhythms influence many of these phenomena. Here we find that a mammalian circadian rhythm component, Cryptochrome 2 (CRY2), regulates E2F family members. Furthermore, CRY1 and CRY2 cooperate with the E3 ligase complex SKP-CULLIN-FBXL3 (SCF(FBXL3)) to reduce E2F steady state protein levels. These findings reveal an unrecognized molecular connection between circadian clocks and cell cycle regulation and highlight another mechanism to maintain appropriate E2F protein levels for proper cell growth.
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spelling pubmed-70580382020-03-12 Cryptochromes modulate E2F family transcription factors Chan, Alanna B. Huber, Anne-Laure Lamia, Katja A. Sci Rep Article Early 2 factor (E2F) family transcription factors participate in myriad cell biological processes including: the cell cycle, DNA repair, apoptosis, development, differentiation, and metabolism. Circadian rhythms influence many of these phenomena. Here we find that a mammalian circadian rhythm component, Cryptochrome 2 (CRY2), regulates E2F family members. Furthermore, CRY1 and CRY2 cooperate with the E3 ligase complex SKP-CULLIN-FBXL3 (SCF(FBXL3)) to reduce E2F steady state protein levels. These findings reveal an unrecognized molecular connection between circadian clocks and cell cycle regulation and highlight another mechanism to maintain appropriate E2F protein levels for proper cell growth. Nature Publishing Group UK 2020-03-05 /pmc/articles/PMC7058038/ /pubmed/32139766 http://dx.doi.org/10.1038/s41598-020-61087-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chan, Alanna B.
Huber, Anne-Laure
Lamia, Katja A.
Cryptochromes modulate E2F family transcription factors
title Cryptochromes modulate E2F family transcription factors
title_full Cryptochromes modulate E2F family transcription factors
title_fullStr Cryptochromes modulate E2F family transcription factors
title_full_unstemmed Cryptochromes modulate E2F family transcription factors
title_short Cryptochromes modulate E2F family transcription factors
title_sort cryptochromes modulate e2f family transcription factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058038/
https://www.ncbi.nlm.nih.gov/pubmed/32139766
http://dx.doi.org/10.1038/s41598-020-61087-y
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