The study of mammalian oocyte competence by transcriptome analysis: progress and challenges

Mol Hum Reprod. 2014 Feb;20(2):103-16. doi: 10.1093/molehr/gat082. Epub 2013 Nov 13.

Abstract

Various morphological and cytological traits of oocytes and their surrounding cumulus cells may be used to select oocytes for assisted reproduction. However, even with careful selection, successful IVF and subsequent embryo development remain uncertain. The factors that ensure oocyte competence are unclear and other approaches to assessing developmental potential must be explored. With the constant development of the molecular toolbox, genomic/transcriptomic analysis is becoming a more and more interesting approach to understand oocyte quality on the basis of RNA composition. Using bovine and mouse models as well as human oocytes of known developmental potential, various efforts are underway to characterize the mRNA profile of the competent oocyte using microarray technology. The proliferation of gene expression data sets raises new opportunities to identify the mechanisms involved in this complex phenotype, which should lead to improved techniques of assisted reproduction. Although several molecular markers of oocyte quality are known, translating these into cellular functions remains challenging, largely due to the poor correlation between mRNA level and protein synthesis. Unlike most somatic cells, the oocyte can store mRNA for days, with transcriptional activity remaining at a halt during the 4-5 days beginning before ovulation and ending with embryonic genome activation. This review provides an overview of the transcriptomic data obtained from oocytes of different quality as well as interesting avenues to explore in order to improve our understanding of oocyte competence.

Keywords: aneuploidy; competence; mRNA; oocyte; quality; transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cattle
  • Cell Survival
  • Female
  • Fertilization in Vitro*
  • Gene Expression
  • Humans
  • Mice
  • Oligonucleotide Array Sequence Analysis
  • Oocytes / cytology
  • Oocytes / growth & development
  • Oocytes / metabolism*
  • Oogenesis / genetics
  • Ovarian Follicle / cytology
  • Ovarian Follicle / growth & development
  • Ovarian Follicle / metabolism*
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Transcriptome*

Substances

  • Biomarkers
  • RNA, Messenger