Inherent Instability of Correct Kinetochore-Microtubule Attachments during Meiosis I in Oocytes

被引:57
|
作者
Yoshida, Shuhei [1 ]
Kaido, Masako [1 ]
Kitajima, Tomoya S. [1 ]
机构
[1] RIKEN Ctr Dev Biol, Lab Chromosome Segregat, Kobe, Hyogo 6500047, Japan
关键词
SPINDLE ASSEMBLY CHECKPOINT; AURORA-B KINASE; CHROMOSOMAL PASSENGER PROTEIN; MOUSE OOCYTES; INTRAKINETOCHORE STRETCH; B56-PP2A PHOSPHATASE; MITOTIC CHECKPOINT; C KINASE; M-PHASE; ACTIVATION;
D O I
10.1016/j.devcel.2015.04.020
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A model for mitosis suggests that correct kineto-chore-microtubule (KT-MT) attachments are stabilized by spatial separation of the attachment sites from Aurora B kinase through sister KT stretching. However, the spatiotemporal regulation of attachment stability during meiosis I (MI) in oocytes remains unclear. Here, we found that in mouse oocytes, Aurora B and C (B/C) are located in close proximity to KT-MT attachment sites after bivalent stretching due to an intrinsic property of the MI chromosomes. The Aurora B/C activity destabilizes correct attachments while allowing a considerable amount of incorrect attachments to form. KT-MT attachments are eventually stabilized through KT dephosphorylation by PP2A-B56 phosphatase, which is progressively recruited to KTs depending on the BubR1 phosphorylation resulting from the timer Cdk1 and independent of bivalent stretching. Thus, oocytes lack a mechanism for coordinating bivalent stretching and KT phosphoregulation during MI, which may explain the high frequency of KT-MT attachment errors.
引用
收藏
页码:589 / 602
页数:14
相关论文
共 50 条
  • [1] Establishing correct kinetochore-microtubule attachments in mitosis and meiosis
    Cairo, Gisela
    Lacefield, Soni
    [J]. KINETOCHORES AND CHROMOSOME SEGREGATION, 2020, 64 (02): : 277 - 287
  • [2] The Error-Prone Kinetochore-Microtubule Attachments During Meiosis I in Vitrified Oocytes
    Gao, Lei
    Hou, Yunpeng
    Zeng, Shenming
    Li, Junyou
    Zhu, Shien
    Fu, Xiangwei
    [J]. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2020, 8
  • [3] Mechanisms to Avoid and Correct Erroneous Kinetochore-Microtubule Attachments
    Lampson, Michael A.
    Grishchuk, Ekaterina L.
    [J]. BIOLOGY-BASEL, 2017, 6 (01):
  • [4] Chromosome Segregation: A Spatial Code to Correct Kinetochore-Microtubule Attachments
    Monda, Julie K.
    Cheeseman, Iain M.
    [J]. CURRENT BIOLOGY, 2015, 25 (14) : R601 - R603
  • [5] Shugoshin Regulates Cohesin, Kinetochore-Microtubule Attachments, and Chromosomal Instability
    Sun, Qiqi
    Liu, Feng
    Mo, Xiaolong
    Yao, Bo
    Liu, Guanghai
    Chen, Shanshan
    Ren, Yanping
    [J]. CYTOGENETIC AND GENOME RESEARCH, 2023, 162 (06) : 283 - 296
  • [6] Increased CDK1 activity determines the timing of kinetochore-microtubule attachments in meiosis I
    Davydenko, Olga
    Schultz, Richard M.
    Lampson, Michael A.
    [J]. JOURNAL OF CELL BIOLOGY, 2013, 202 (02): : 221 - 229
  • [7] FORMIN Stable Kinetochore-Microtubule Attachments
    Wiggan, O'Neil
    DeLuca, Jennifer G.
    [J]. DEVELOPMENTAL CELL, 2011, 20 (03) : 283 - 284
  • [8] Mechanical quality control of kinetochore-microtubule attachments during prometaphase
    Auckland, P.
    McAinsh, A. D.
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2015, 26
  • [9] Stable kinetochore-microtubule attachments restrict MTOC position and spindle elongation in oocytes
    Courtois, Aurelien
    Yoshida, Shuhei
    Takenouchi, Osamu
    Asai, Kohei
    Kitajima, Tomoya S.
    [J]. EMBO REPORTS, 2021, 22 (04)
  • [10] Kinetochore-microtubule attachments as a precision therapy target
    Herman, Jacob A.
    Paddison, Patrick J.
    DeLuca, Jennifer
    Olson, James
    [J]. MOLECULAR CANCER RESEARCH, 2016, 14