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Scc1/Rad21/Mcd1 Is Required for Sister Chromatid Cohesion and Kinetochore Function in Vertebrate Cells

  • Eiichiro Sonoda
  • , Takahiro Matsusaka
  • , Ciaran Morrison
  • , Paola Vagnarelli
  • , Osamu Hoshi
  • , Tatsuo Ushiki
  • , Kuniharu Nojima
  • , Tatsuo Fukagawa
  • , Irene C. Waizenegger
  • , Jan Michael Peters
  • , William C. Earnshaw
  • , Shunichi Takeda
  • Japan Sci. Technol. Corp. (JST), N.
  • Kyoto University
  • University of Edinburgh
  • Fac. Med., Niigata Univ., 951-8510
  • Res. Inst. of Molecular Pathology

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

250 Citations (Scopus)

Abstract

Proteolytic cleavage of the cohesin subunit Scc1 is a consistent feature of anaphase onset, although temporal differences exist between eukaryotes in cohesin loss from chromosome arms, as distinct from centromeres. We describe the effects of genetic deletion of Scc1 in chicken DT40 cells. Scc1 loss caused premature sister chromatid separation but did not disrupt chromosome condensation. Scc1 mutants showed defective repair of spontaneous and induced DNA damage. Scc1-deficient cells frequently failed to complete metaphase chromosome alignment and showed chromosome segregation defects, suggesting aberrant kinetochore function. Notably, the chromosome passenger INCENP did not localize normally to centromeres, while the constitutive kinetochore proteins CENP-C and CENP-H behaved normally. These results suggest a role for Scc1 in mitotic regulation, along with cohesion.

Original languageEnglish
Pages (from-to)759-770
Number of pages12
JournalDevelopmental Cell
Volume1
Issue number6
DOIs
Publication statusPublished - Dec 2001
Externally publishedYes

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