Molecular basis of chromosome segregation and age-associated errors in oocyte meiosis I

Oocyte meiosis determines chromosomes that are transmitted from the mother to the next generation. The molecular mechanisms underlying meiotic chromosome segregation are organized in distinct chromosomal regions-the core centromere, peri-centromere, and chromosome arms. A common molecular basis for mechanisms operating in these distinct regions is Rec8 cohesin, together with cooperating regulatory pathways. This Review describes Rec8-cohesin-based mechanisms operating in each chromosomal region and discusses how these mechanisms work coordinately to achieve chromosome segregation during meiosis I, focusing primarily on insights from studies using mouse oocytes as a model system. Based on this molecular understanding, it further discusses how age-associated decline of chromosomal Rec8 cohesin can lead to chromosome segregation errors, a major cause of infertility, miscarriage, and congenital disorders.

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Publication Details

Journal
Biology of Reproduction
Published
2026-04-24
DOI
https://doi.org/10.1093/biolre/ioag086
Primary Topic
Microtubule and mitosis dynamics
Type
article
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article

Molecular basis of chromosome segregation and age-associated errors in oocyte meiosis I

Tomoya S. Kitajima
Biology of Reproduction
Microtubule and mitosis dynamics
article

Molecular basis of chromosome segregation and age-associated errors in oocyte meiosis I

Tomoya S. Kitajima
article en

Abstract

Oocyte meiosis determines chromosomes that are transmitted from the mother to the next generation. The molecular mechanisms underlying meiotic chromosome segregation are organized in distinct chromosomal regions-the core centromere, peri-centromere, and chromosome arms. A common molecular basis for mechanisms operating in these distinct regions is Rec8 cohesin, together with cooperating regulatory pathways. This Review describes Rec8-cohesin-based mechanisms operating in each chromosomal region and discusses how these mechanisms work coordinately to achieve chromosome segregation during meiosis I, focusing primarily on insights from studies using mouse oocytes as a model system. Based on this molecular understanding, it further discusses how age-associated decline of chromosomal Rec8 cohesin can lead to chromosome segregation errors, a major cause of infertility, miscarriage, and congenital disorders.

Biology of Reproduction
RIKEN Center for Biosystems Dynamics Research (JP)
Openalex Percentile: Top 19%
Microtubule and mitosis dynamics
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