FRONTIER QUESTIONS ABOUT SISTER-CHROMATID SEPARATION IN ANAPHASE

被引:43
作者
YANAGIDA, N
机构
[1] Department of Biophysics, Faculty of Science, Kyoto University, Kyoto, 606, Sakyo-ku
关键词
D O I
10.1002/bies.950170608
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sister chromatid separation in anaphase is an important event in the cell's transmission of genetic information to a descendent. It has been investigated from different aspects: cell cycle regulation, spindle and chromosome dynamics within the three-dimensional cell architecture, transmission fidelity control and cellular signaling. Integrated studies directed toward unified understanding are possible using multidisciplinary methods with model organisms. Ubiquitin-dependent proteolysis, protein dephosphorylation, an unknown function by the TPR repeat proteins, chromosome transport by microtubule-based motors and DNA topological change by DNA topoisomerase II are all necessary for progression from metaphase to anaphase. Chromosome condensation, mitotic kinetochore function and spindle formation require a large number of proteins, which are prerequisites for successful sister chromatid separation. Factors that help to retain sister chromatid connection after replication and prevent premature separation remain to be determined. Although sister chromatid separation occurs in anaphase, gene functions in other cell cycle stages also ensure the progression of correct chromatid separation.
引用
收藏
页码:519 / 526
页数:8
相关论文
共 70 条
  • [1] CENTROSOME AND KINETOCHORE MOVEMENT DURING MITOSIS
    AULT, JG
    RIEDER, CL
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (01) : 41 - 49
  • [2] ONE OF THE PROTEIN PHOSPHATASE-1 ISOENZYMES IN DROSOPHILA IS ESSENTIAL FOR MITOSIS
    AXTON, JM
    DOMBRADI, V
    COHEN, PTW
    GLOVER, DM
    [J]. CELL, 1990, 63 (01) : 33 - 46
  • [3] THE CENTROMERIC K-TYPE REPEAT AND THE CENTRAL CORE ARE TOGETHER SUFFICIENT TO ESTABLISH A FUNCTIONAL SCHIZOSACCHAROMYCES-POMBE CENTROMERE
    BAUM, M
    NGAN, VK
    CLARKE, L
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (07) : 747 - 761
  • [4] DPY-27 - A CHROMOSOME CONDENSATION PROTEIN HOMOLOG THAT REGULATES C. ELEGANS DOSAGE COMPENSATION THROUGH ASSOCIATION WITH THE X-CHROMOSOME
    CHUANG, PT
    ALBERTSON, DG
    MEYER, BJ
    [J]. CELL, 1994, 79 (03) : 459 - 474
  • [5] PHOSPHORYLATION AND INACTIVATION OF PROTEIN PHOSPHATASE-1 BY CYCLIN-DEPENDENT KINASES
    DOHADWALA, M
    SILVA, EFDE
    HALL, FL
    WILLIAMS, RT
    CARBONAROHALL, DA
    NAIRN, AC
    GREENGARD, P
    BERNDT, N
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) : 6408 - 6412
  • [6] DOONAN JH, 1992, J CELL SCI, V103, P599
  • [7] FARUKI S, 1992, J CELL SCI, V101, P69
  • [8] A CONSERVED MITOTIC KINASE ACTIVE AT LATE ANAPHASE TELOPHASE IN SYNCYTIAL DROSOPHILA EMBRYOS
    FENTON, B
    GLOVER, DM
    [J]. NATURE, 1993, 363 (6430) : 637 - 640
  • [9] TYPE-1 PROTEIN PHOSPHATASE ACTS IN OPPOSITION TO IPL1 PROTEIN-KINASE IN REGULATING YEAST CHROMOSOME SEGREGATION
    FRANCISCO, L
    WANG, WF
    CHAN, CSM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) : 4731 - 4740
  • [10] FRANKHAUSER C, 1993, EMBO J, V12, P2697