Differential activation of the DNA replication checkpoint contributes to asynchrony of cell division in C. elegans embryos.

Détails

ID Serval
serval:BIB_28405
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Differential activation of the DNA replication checkpoint contributes to asynchrony of cell division in C. elegans embryos.
Périodique
Current Biology
Auteur⸱e⸱s
Brauchle M., Baumer K., Gönczy P.
ISSN
0960-9822
Statut éditorial
Publié
Date de publication
2003
Volume
13
Numéro
10
Pages
819-827
Langue
anglais
Résumé
BACKGROUND: Acquisition of lineage-specific cell cycle duration is a central feature of metazoan development. The mechanisms by which this is achieved during early embryogenesis are poorly understood. In the nematode Caenorhabditis elegans, differential cell cycle duration is apparent starting at the two-cell stage, when the larger anterior blastomere AB divides before the smaller posterior blastomere P(1). How anterior-posterior (A-P) polarity cues control this asynchrony remains to be elucidated.RESULTS: We establish that early C. elegans embryos possess a hitherto unrecognized DNA replication checkpoint that relies on the PI-3-like kinase atl-1 and the kinase chk-1. We demonstrate that preferential activation of this checkpoint in the P(1) blastomere contributes to asynchrony of cell division in two-cell-stage wild-type embryos. Furthermore, we show that preferential checkpoint activation is largely abrogated in embryos that undergo equal first cleavage following inactivation of Galpha signaling.CONCLUSION: Our findings establish that differential checkpoint activation contributes to acquisition of distinct cell cycle duration in two-cell-stage C. elegans embryos and suggest a novel mechanism coupling asymmetric division to acquisition of distinct cell cycle duration during development.
Mots-clé
Animals, Animals, Genetically Modified, Blastomeres/physiology, Caenorhabditis elegans/cytology, Caenorhabditis elegans/embryology, Caenorhabditis elegans Proteins/metabolism, Cell Cycle Proteins/metabolism, Cell Division/physiology, Cell Polarity/genetics, Chromosome Segregation/drug effects, Chromosome Segregation/physiology, DNA Replication/genetics, DNA Replication/physiology, GTP-Binding Protein alpha Subunits/metabolism, Hydroxyurea/pharmacology, Microscopy/methods, Microscopy, Fluorescence, Mitosis/physiology, Phosphotransferases/metabolism, Protein Kinases/metabolism, S Phase/physiology, Signal Transduction
Pubmed
Web of science
Open Access
Oui
Création de la notice
19/11/2007 12:25
Dernière modification de la notice
20/08/2019 13:07
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