Literature DB >> 26255654

How oocytes try to get it right: spindle checkpoint control in meiosis.

Sandra A Touati1,2,3, Katja Wassmann4,5.   

Abstract

The generation of a viable, diploid organism depends on the formation of haploid gametes, oocytes, and spermatocytes, with the correct number of chromosomes. Halving the genome requires the execution of two consecutive specialized cell divisions named meiosis I and II. Unfortunately, and in contrast to male meiosis, chromosome segregation in oocytes is error prone, with human oocytes being extraordinarily "meiotically challenged". Aneuploid oocytes, that are with the wrong number of chromosomes, give rise to aneuploid embryos when fertilized. In humans, most aneuploidies are lethal and result in spontaneous abortions. However, some trisomies survive to birth or even adulthood, such as the well-known trisomy 21, which gives rise to Down syndrome (Nagaoka et al. in Nat Rev Genet 13:493-504, 2012). A staggering 20-25 % of oocytes ready to be fertilized are aneuploid in humans. If this were not bad enough, there is an additional increase in meiotic missegregations as women get closer to menopause. A woman above 40 has a risk of more than 30 % of getting pregnant with a trisomic child. Worse still, in industrialized western societies, child birth is delayed, with women getting their first child later in life than ever. This trend has led to an increase of trisomic pregnancies by 70 % in the last 30 years (Nagaoka et al. in Nat Rev Genet 13:493-504, 2012; Schmidt et al. in Hum Reprod Update 18:29-43, 2012). To understand why errors occur so frequently during the meiotic divisions in oocytes, we review here the molecular mechanisms at works to control chromosome segregation during meiosis. An important mitotic control mechanism, namely the spindle assembly checkpoint or SAC, has been adapted to the special requirements of the meiotic divisions, and this review will focus on our current knowledge of SAC control in mammalian oocytes. Knowledge on how chromosome segregation is controlled in mammalian oocytes may help to identify risk factors important for questions related to human reproductive health.

Entities:  

Keywords:  Aneuploidy; Cohesin protection; Meiosis; Monopolar attachment; Mouse oocytes; Spindle assembly checkpoint

Mesh:

Year:  2015        PMID: 26255654     DOI: 10.1007/s00412-015-0536-7

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  129 in total

1.  Spindle assembly checkpoint signalling is uncoupled from chromosomal position in mouse oocytes.

Authors:  Liming Gui; Hayden Homer
Journal:  Development       Date:  2012-04-18       Impact factor: 6.868

2.  Oocyte-specific differences in cell-cycle control create an innate susceptibility to meiotic errors.

Authors:  So Iha Nagaoka; Craig A Hodges; David F Albertini; Patricia Ann Hunt
Journal:  Curr Biol       Date:  2011-04-14       Impact factor: 10.834

Review 3.  [Meiotic weakness: the first division].

Authors:  M Emilie Terret; Katja Wassmann
Journal:  Med Sci (Paris)       Date:  2008-02       Impact factor: 0.818

Review 4.  The spindle assembly checkpoint: progress and persistent puzzles.

Authors:  Silke Hauf
Journal:  Biochem Soc Trans       Date:  2013-12       Impact factor: 5.407

5.  Aurora-C kinase supports mitotic progression in the absence of Aurora-B.

Authors:  Scott D Slattery; Michael A Mancini; Bill R Brinkley; Rebecca M Hall
Journal:  Cell Cycle       Date:  2009-09-21       Impact factor: 4.534

6.  BubR1 is a spindle assembly checkpoint protein regulating meiotic cell cycle progression of mouse oocyte.

Authors:  Liang Wei; Xing-Wei Liang; Qing-Hua Zhang; Mo Li; Ju Yuan; Sen Li; Shao-Chen Sun; Ying-Chun Ouyang; Heide Schatten; Qing-Yuan Sun
Journal:  Cell Cycle       Date:  2010-03-15       Impact factor: 4.534

7.  Nuclear pores protect genome integrity by assembling a premitotic and Mad1-dependent anaphase inhibitor.

Authors:  Veronica Rodriguez-Bravo; John Maciejowski; Jennifer Corona; Håkon Kirkeby Buch; Philippe Collin; Masato T Kanemaki; Jagesh V Shah; Prasad V Jallepalli
Journal:  Cell       Date:  2014-02-27       Impact factor: 41.582

8.  Ageing-associated aberration in meiosis of oocytes from senescence-accelerated mice.

Authors:  Lin Liu; David L Keefe
Journal:  Hum Reprod       Date:  2002-10       Impact factor: 6.918

9.  Sensing chromosome bi-orientation by spatial separation of aurora B kinase from kinetochore substrates.

Authors:  Dan Liu; Gerben Vader; Martijn J M Vromans; Michael A Lampson; Susanne M A Lens
Journal:  Science       Date:  2009-01-15       Impact factor: 47.728

Review 10.  The spindle-assembly checkpoint in space and time.

Authors:  Andrea Musacchio; Edward D Salmon
Journal:  Nat Rev Mol Cell Biol       Date:  2007-04-11       Impact factor: 94.444

View more
  29 in total

Review 1.  Chromothripsis, a credible chromosomal mechanism in evolutionary process.

Authors:  Franck Pellestor; Vincent Gatinois
Journal:  Chromosoma       Date:  2018-08-07       Impact factor: 4.316

2.  Special issue on "recent advances in meiotic chromosome structure, recombination and segregation".

Authors:  Marco Barchi; Paula Cohen; Scott Keeney
Journal:  Chromosoma       Date:  2016-03-29       Impact factor: 4.316

3.  Cycling through mammalian meiosis: B-type cyclins in oocytes.

Authors:  Nora Bouftas; Katja Wassmann
Journal:  Cell Cycle       Date:  2019-06-23       Impact factor: 4.534

Review 4.  Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events.

Authors:  Marco Conti; Federica Franciosi
Journal:  Hum Reprod Update       Date:  2018-05-01       Impact factor: 15.610

Review 5.  The resolution of ambiguity as the basis for life: A cellular bridge between Western reductionism and Eastern holism.

Authors:  John S Torday; William B Miller
Journal:  Prog Biophys Mol Biol       Date:  2017-07-22       Impact factor: 3.667

6.  Prdm9 deficiency of rat oocytes causes synapsis among non-homologous chromosomes and aneuploidy.

Authors:  Srdjan Gasic; Ondrej Mihola; Zdenek Trachtulec
Journal:  Mamm Genome       Date:  2022-05-20       Impact factor: 2.957

7.  Self-organization of kinetochore-fibers in human mitotic spindles.

Authors:  William Conway; Robert Kiewisz; Gunar Fabig; Colm P Kelleher; Hai-Yin Wu; Maya Anjur-Dietrich; Thomas Müller-Reichert; Daniel J Needleman
Journal:  Elife       Date:  2022-07-25       Impact factor: 8.713

Review 8.  The process of ovarian aging: it is not just about oocytes and granulosa cells.

Authors:  Antonella Camaioni; Maria Assunta Ucci; Luisa Campagnolo; Massimo De Felici; Francesca Gioia Klinger
Journal:  J Assist Reprod Genet       Date:  2022-04       Impact factor: 3.357

9.  Rab6a is a novel regulator of meiotic apparatus and maturational progression in mouse oocytes.

Authors:  Xiaojing Hou; Jiaqi Zhang; Ling Li; Rujun Ma; Juan Ge; Longsen Han; Qiang Wang
Journal:  Sci Rep       Date:  2016-02-26       Impact factor: 4.379

Review 10.  Multiple Duties for Spindle Assembly Checkpoint Kinases in Meiosis.

Authors:  Adele L Marston; Katja Wassmann
Journal:  Front Cell Dev Biol       Date:  2017-12-13
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.