Zw10 is a spindle assembly checkpoint protein that regulates meiotic maturation in mouse oocytes

被引:5
作者
Park, Yuram [1 ]
Kim, Jae-Sung [2 ]
Oh, Jeong Su [1 ]
机构
[1] Sungkyunkwan Univ, Dept Integrat Biotechnol, Coll Biotechnol & Bioengn, Suwon 440746, Gyeonggi Do, South Korea
[2] Korea Inst Radiol & Med Sci, Div Radiat Canc Res, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Oocyte; Spindle assembly checkpoint; Zw10; Kinetochore; Chromosome segregation; MATERNAL AGE; ROUGH-DEAL; ENDOPLASMIC-RETICULUM; MEMBRANE TRAFFICKING; MEIOSIS-II; CYCLIN-B; CHROMOSOME; EXPRESSION; ANAPHASE; MAD2;
D O I
10.1007/s00418-019-01800-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Faithful chromosome segregation during the cell cycle is ensured by the spindle assembly checkpoint (SAC). Although SAC activity is highly conserved and most organisms share common SAC components, additional proteins that regulate SAC activity to ensure high fidelity chromosome segregation are present in higher eukaryotes. Zw10 is one of these additional SAC components. Although Zw10 has been demonstrated to be involved in SAC activity during mitosis, little is known about its role during oocyte meiosis. Here, we report that Zw10 is localized at the kinetochore and is required for SAC activation during meiotic maturation. Knockdown of Zw10 led to precocious polar body extrusion by impairing Mad2 recruitment at kinetochores. Moreover, Zw10 knockdown impaired chromosome alignment and kinetochore-microtubule attachment, increasing the incidence of aneuploidy. Furthermore, Zw10 expression decreased with maternal age, suggesting that Zw10 is associated with the age-related increase in the incidence of aneuploidy. Together, our results demonstrate that Zw10 is localized at kinetochores and functions as an essential SAC component in mouse oocytes.
引用
收藏
页码:207 / 215
页数:9
相关论文
共 39 条
[1]   BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice [J].
Baker, DJ ;
Jeganathan, KB ;
Cameron, JD ;
Thompson, M ;
Juneja, S ;
Kopecka, A ;
Kumar, R ;
Jenkins, RB ;
de Groen, PC ;
Roche, P ;
van Deursen, JM .
NATURE GENETICS, 2004, 36 (07) :744-749
[2]   Rough deal and Zw10 are required for the metaphase checkpoint in Drosophila [J].
Basto, R ;
Gomes, R ;
Karess, RE .
NATURE CELL BIOLOGY, 2000, 2 (12) :939-943
[3]  
Bharadwaj R, 2016, ONCOGENE, V23, P11
[4]   Recruitment of Mad2 to the kinetochore requires the Rod/Zw10 complex [J].
Buffin, E ;
Lefebvre, C ;
Huang, JY ;
Gagou, ME ;
Karess, RE .
CURRENT BIOLOGY, 2005, 15 (09) :856-861
[5]   Human Zw10 and ROD ave mitotic checkpoint proteins that bind to kinetochores [J].
Chan, GKT ;
Jablonski, SA ;
Starr, DA ;
Goldberg, ML ;
Yen, TJ .
NATURE CELL BIOLOGY, 2000, 2 (12) :944-947
[6]   Molecular architecture of the kinetochore-microtubule interface [J].
Cheeseman, Iain M. ;
Desai, Arshad .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (01) :33-46
[7]  
Dailey T, 1996, AM J HUM GENET, V59, P176
[8]   The spindle checkpoint: two transitions, two pathways [J].
Gardner, RD ;
Burke, DJ .
TRENDS IN CELL BIOLOGY, 2000, 10 (04) :154-158
[9]   To ERR (meiotically) is human: The genesis of human aneuploidy [J].
Hassold, T ;
Hunt, P .
NATURE REVIEWS GENETICS, 2001, 2 (04) :280-291
[10]   Implication of ZW10 in membrane trafficking between the endoplasmic reticulum and Golgi [J].
Hirose, H ;
Arasaki, K ;
Dohmae, N ;
Takio, K ;
Hatsuzawa, K ;
Nagahama, M ;
Tani, K ;
Yamamoto, A ;
Tohyama, M ;
Tagaya, M .
EMBO JOURNAL, 2004, 23 (06) :1267-1278