Separase: a universal trigger for sister chromatid disjunction but not chromosome cycle progression

Autor: Nobuaki Kudo, Jan-Michael Peters, Germain M. Ducos, Nicole Firnberg, Karin G. Wirth, Anders Zetterberg, Chantal Desdouets, Gordana Wutz, Romeo Ricci, Kim Nasmyth, Janina Seznec, Shahryar Taghybeeglu
Přispěvatelé: Ricci, Romeo, Research Institute of Molecular Pathology (IMP), Friedrich-Schiller-Universität = Friedrich Schiller University Jena [Jena, Germany], Institut Cochin (IC UM3 (UMR 8104 / U1016)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Karolinska Institute, Eidgenössische Technische Hochschule - Swiss Federal Institute of Technology [Zürich] (ETH Zürich)
Rok vydání: 2006
Předmět:
Male
Chromosomal Proteins
Non-Histone

[SDV]Life Sciences [q-bio]
Cell Cycle Proteins
SACCHAROMYCES-CEREVISIAE
Mice
Chromosome Segregation
11 Medical and Health Sciences
Research Articles
Anaphase
Mice
Knockout

Cell Cycle
Nuclear Proteins
DROSOPHILA SEPARASE
Cell biology
[SDV] Life Sciences [q-bio]
Securin
Establishment of sister chromatid cohesion
METAPHASE
COMPLEXES
Female
Chromatid
Separase
Life Sciences & Biomedicine
COHESIN
DNA Replication Timing
Embryonic Development
Mitosis
FISSION YEAST
Biology
Article
Cell Line
Polyploidy
Endopeptidases
Animals
Sister chromatids
Science & Technology
Cohesin
CLEAVAGE
Cell Biology
06 Biological Sciences
Fibroblasts
Hematopoietic Stem Cells
Molecular biology
ANAPHASE TRANSITION
Liver Regeneration
SPINDLE
Hepatocytes
Genes
Lethal

Carrier Proteins
Developmental Biology
Zdroj: The Journal of Cell Biology
Journal of Cell Biology
Journal of Cell Biology, 2006, 172 (6), pp.847-860. ⟨10.1083/jcb.200506119⟩
ISSN: 1540-8140
0021-9525
DOI: 10.1083/jcb.200506119
Popis: International audience; Separase is a protease whose liberation from its inhibitory chaperone Securin triggers sister chromatid disjunction at anaphase onset in yeast by cleaving cohesin's kleisin subunit. We have created conditional knockout alleles of the mouse Separase and Securin genes. Deletion of both copies of Separase but not Securin causes embryonic lethality. Loss of Securin reduces Separase activity because deletion of just one copy of the Separase gene is lethal to embryos lacking Securin. In embryonic fibroblasts, Separase depletion blocks sister chromatid separation but does not prevent other aspects of mitosis, cytokinesis, or chromosome replication. Thus, fibroblasts lacking Separase become highly polyploid. Hepatocytes stimulated to proliferate in vivo by hepatectomy also become unusually large and polyploid in the absence of Separase but are able to regenerate functional livers. Separase depletion in bone marrow causes aplasia and the presumed death of hematopoietic cells other than erythrocytes. Destruction of sister chromatid cohesion by Separase may be a universal feature of mitosis in eukaryotic cells.
Databáze: OpenAIRE