Molecular basis of maternal age-related increase in oocyte aneuploidy

Hiroki Kurahashi, Makiko Tsutsumi, Sachie Nishiyama, Hiroshi Kogo, Hidehito Inagaki, Tamae Ohye

研究成果: Article査読

28 被引用数 (Scopus)

抄録

Aneuploidy is one of the most common and serious pregnancy complications in humans. Most conceptuses with autosomal aneuploidy die in utero, resulting in early pregnancy loss. However, some fetuses with aneuploidy survive to term but suffer from disorders associated with congenital anomalies and mental retardation, such as Down syndrome with trisomy 21. Three general characteristics of this condition are well acknowledged: (i) in most cases the extra chromosome is of maternal origin; (ii) most cases are derived from a malsegregation event in meiosis I; and (iii) the frequency of these errors increases with maternal age. The basis for the age-dependent increase in meiosis I errors has been a long-standing enigma. Many investigators have addressed the nature of this biological phenomenon through genomic analyses of extra chromosome 21 using polymorphic markers to determine the frequency or location of crossovers that should ensure faithful chromosome segregation. Cytogenetic analyses of in vitro unfertilized oocytes have also been performed. However, no definitive conclusions regarding meiosis I errors have yet been reached from such studies. Recent findings in conditional knock-out mice for meiosis-specific cohesin have shed further light on this issue. The present review focuses on the current understanding of age-related aneuploidy and provides an overview of the mechanisms involved. We refer to recent data to illustrate some of the new paradigms that have arisen in this field.

本文言語English
ページ(範囲)8-15
ページ数8
ジャーナルCongenital anomalies
52
1
DOI
出版ステータスPublished - 03-2012

All Science Journal Classification (ASJC) codes

  • 医学(全般)

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