New insights into the regulation of anaphase by mitotic cyclins in budding yeast

被引:7
作者
Signon, Laurence [1 ,2 ]
机构
[1] Univ Paris 11, CNRS, UMR8621, Inst Genet & Microbiol, F-91405 Orsay, France
[2] CNRS, Lab Ingn Syst Macromol, UPR9027, Marseille, France
关键词
mitotic cyclins; chromosome segregation; anaphase; microtubules; DNA damage; budding yeast; DNA-DAMAGE CHECKPOINT; SACCHAROMYCES-CEREVISIAE; CELL-CYCLE; CHROMOSOME MOVEMENT; MICROTUBULE INTERACTIONS; SPINDLE ORIENTATION; DEPENDENT KINASES; MITOSIS; KINETOCHORE; SEPARATION;
D O I
10.4161/cc.10.10.15632
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitotic cyclins drive initiation and progression through mitosis. However, their role during progression remains poorly understood, due to their essential function in initiation of mitosis and redundant activities. The function of the principal mitotic cyclin Clb2, in S. cerevisiae, was investigated during progression through anaphase in diploid cells, after DNA damage and during normal growth using fixed and live cell fluorescence techniques. I find that during anaphase, absence of Clb2 affects chromosome movement and plays an important role in inhibiting kinetochore microtubules regrowth. In addition, absence of Clb2 leads to defects and collapse of spindle pole body separation. Most unexpectedly, new bipolar spindle forms and spindle re-forms. The intensity of the defects appears to correlate with strength of checkpoint activation and while during adaptation to DNA damage, these defects lead to important chromosome missegregation, during normal growth, defects are resolved rapidly. During recovery, intermediate phenotypes are observed. Alltogether, data reveal new and unexpected roles for mitotic cyclins during progression through mitosis: results indicate that mitotic cyclins play key role in growth suppression of kinetochore microtubules and suggest that new bipolar spindle formation might be actively inhibited by mitotic cyclins during anaphase.
引用
收藏
页码:1655 / 1668
页数:14
相关论文
共 69 条
  • [1] Microtubule interactions with the cell cortex causing nuclear movements in Saccharomyces cerevisiae
    Adames, NR
    Cooper, JA
    [J]. JOURNAL OF CELL BIOLOGY, 2000, 149 (04) : 863 - 874
  • [2] AIST JR, 1993, J CELL SCI, V104, P1207
  • [3] MECHANICS OF CHROMOSOME SEPARATION DURING MITOSIS IN FUSARIUM (FUNGI IMPERFECTI) - NEW EVIDENCE FROM ULTRASTRUCTURAL AND LASER MICROBEAM EXPERIMENTS
    AIST, JR
    BERNS, MW
    [J]. JOURNAL OF CELL BIOLOGY, 1981, 91 (02) : 446 - 458
  • [4] CENTROSOME AND KINETOCHORE MOVEMENT DURING MITOSIS
    AULT, JG
    RIEDER, CL
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (01) : 41 - 49
  • [5] Differential cellular localization among mitotic cyclins from Saccharomyces cerevisiae:: a new role for the axial budding protein Bud3 in targeting Clb2 to the mother-bud neck
    Bailly, E
    Cabantous, S
    Sondaz, D
    Bernadac, A
    Simon, MN
    [J]. JOURNAL OF CELL SCIENCE, 2003, 116 (20) : 4119 - 4130
  • [6] An ATM and ATR dependent pathway targeting centrosome dependent spindle assembly
    Brown, Nicola
    Costanzo, Vincenzo
    [J]. CELL CYCLE, 2009, 8 (13) : 1997 - 2001
  • [7] Microtubules orient the mitotic spindle in yeast through dynein-dependent interactions with the cell cortex
    Carminati, JL
    Stearns, T
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 138 (03) : 629 - 641
  • [8] Cyclin B1 is localized to unattached kinetochores and contributes to efficient microtubule attachment and proper chromosome alignment during mitosis
    Chen, Qiang
    Zhang, Xiaoyan
    Jiang, Qing
    Clarke, Paul R.
    Zhang, Chuamnao
    [J]. CELL RESEARCH, 2008, 18 (02) : 268 - 280
  • [9] S-phase checkpoint controls mitosis via an APC-independent Cdc20p function
    Clarke, DJ
    Segal, M
    Andrews, CA
    Rudyak, SG
    Jensen, S
    Smith, K
    Reed, SI
    [J]. NATURE CELL BIOLOGY, 2003, 5 (10) : 928 - 935
  • [10] The anaphase inhibitor of Saccharomyces cerevisiae Pds1p is a target of the DNA damage checkpoint pathway
    Cohen-Fix, O
    Koshland, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) : 14361 - 14366