Short communication: expression and alternative splicing of POU1F1 pathway genes in preimplantation bovine embryos

J Dairy Sci. 2011 Aug;94(8):4220-3. doi: 10.3168/jds.2011-4144.

Abstract

Early embryo loss is a major contributing factor to cow infertility and that 70 to 80% of this loss occurs between d 8 and 16 postfertilization. However, little is known about the molecular mechanisms and the nature of genes involved in normal and abnormal embryonic development. Moreover, information is limited on the contributions of the genomes of dams and of embryos to the development and survival of preimplantation embryos. We hypothesized that proper gene expression level in the developing embryo is essential for embryo survival and pregnancy success. As such, the characterization of expression profiles in early embryos could lead to a better understanding of the mechanisms involved in normal and abnormal embryo development. To test this hypothesis, 2 d-8 embryo populations (degenerate embryos and blastocysts) that differed in morphology and developmental status were investigated. Expression levels of POU1F1 pathway genes were estimated in 4 sets of biological replicate pools of degenerate embryos and blastocysts. The OPN and STAT5A genes were found to be upregulated in degenerate embryos compared with blastocysts, whereas STAT5B showed similar expression levels in both embryo groups. Analysis of splice variants of OPN and STAT5A revealed expression patterns different from the total expression values of these genes. As such, measuring expression of individual transcripts should be considered in gene expression studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics*
  • Animals
  • Blastocyst / metabolism*
  • Cattle / genetics*
  • Female
  • Fertility / genetics
  • Fertilization / genetics
  • Gene Expression / genetics*
  • Genes / genetics
  • Genotype
  • Pregnancy
  • Transcription Factor Pit-1 / genetics*
  • Transcription Factor Pit-1 / physiology

Substances

  • Transcription Factor Pit-1