Allele-specific expression of the MAOA gene and X chromosome inactivation in in vitro produced bovine embryos

Mol Reprod Dev. 2010 Jul;77(7):615-21. doi: 10.1002/mrd.21192.

Abstract

During embryogenesis, one of the two X chromosomes is inactivated in embryos. The production of embryos in vitro may affect epigenetic mechanisms that could alter the expression of genes related to embryo development and X chromosome inactivation (XCI). The aim of this study was to understand XCI during in vitro, pre-implantation bovine embryo development by characterizing the allele-specific expression pattern of the X chromosome-linked gene, monoamine oxidase A (MAOA). Two pools of ten embryos, comprised of the 4-, 8- to 16-cell, morula, blastocyst, and expanded blastocyst stages, were collected. Total RNA from embryos was isolated, and the RT-PCR-RFLP technique was used to observe expression of the MAOA gene. The DNA amplicons were also sequenced using the dideoxy sequencing method. MAOA mRNA was detected, and allele-specific expression was identified in each pool of embryos. We showed the presence of both the maternal and paternal alleles in the 4-, 8- to 16-cell, blastocyst and expanded blastocyst embryos, but only the maternal allele was present in the morula stage. Therefore, we can affirm that the paternal X chromosome is totally inactivated at the morula stage and reactivated at the blastocyst stage. To our knowledge, this is the first report of allele-specific expression of an X-linked gene that is subject to XCI in in vitro bovine embryos from the 4-cell to expanded blastocyst stages. We have established a pattern of XCI in our in vitro embryo production system that can be useful as a marker to assist the development of new protocols for in vitro embryo production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Blastocyst / metabolism
  • Blastocyst / physiology*
  • Cattle
  • Cumulus Cells
  • DNA Methylation
  • Female
  • Gene Expression Profiling
  • Male
  • Monoamine Oxidase / genetics*
  • Monoamine Oxidase / metabolism
  • Phenotype
  • Polymorphism, Restriction Fragment Length
  • RNA, Messenger / chemistry
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • X Chromosome Inactivation / genetics*

Substances

  • RNA, Messenger
  • Monoamine Oxidase