Separase and Roads to Disengage Sister Chromatids during Anaphase
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
Grantová podpora
20-25850S
Czech Science Foundation
RO 0518
Ministry of Agriculture
PubMed
36902034
PubMed Central
PMC10003635
DOI
10.3390/ijms24054604
PII: ijms24054604
Knihovny.cz E-zdroje
- Klíčová slova
- CDK1, Cyclin B1, Mad2, Sgo2, aneuploidy, chromosome division, cohesin, securin, segregation errors, separase,
- MeSH
- anafáze * MeSH
- aparát dělícího vřeténka metabolismus MeSH
- chromatidy * metabolismus MeSH
- mitóza MeSH
- proteiny buněčného cyklu metabolismus MeSH
- segregace chromozomů MeSH
- separasa genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- proteiny buněčného cyklu MeSH
- separasa MeSH
Receiving complete and undamaged genetic information is vital for the survival of daughter cells after chromosome segregation. The most critical steps in this process are accurate DNA replication during S phase and a faithful chromosome segregation during anaphase. Any errors in DNA replication or chromosome segregation have dire consequences, since cells arising after division might have either changed or incomplete genetic information. Accurate chromosome segregation during anaphase requires a protein complex called cohesin, which holds together sister chromatids. This complex unifies sister chromatids from their synthesis during S phase, until separation in anaphase. Upon entry into mitosis, the spindle apparatus is assembled, which eventually engages kinetochores of all chromosomes. Additionally, when kinetochores of sister chromatids assume amphitelic attachment to the spindle microtubules, cells are finally ready for the separation of sister chromatids. This is achieved by the enzymatic cleavage of cohesin subunits Scc1 or Rec8 by an enzyme called Separase. After cohesin cleavage, sister chromatids remain attached to the spindle apparatus and their poleward movement on the spindle is initiated. The removal of cohesion between sister chromatids is an irreversible step and therefore it must be synchronized with assembly of the spindle apparatus, since precocious separation of sister chromatids might lead into aneuploidy and tumorigenesis. In this review, we focus on recent discoveries concerning the regulation of Separase activity during the cell cycle.
Department of Genetics and Reproduction Veterinary Research Institute 621 00 Brno Czech Republic
Faculty of Science Masaryk University 602 00 Brno Czech Republic
Institute of Animal Physiology and Genetics Czech Academy of Science 277 21 Libechov Czech Republic
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