Global assessment of imprinted gene expression in the bovine conceptus by next generation sequencing

Epigenetics. 2016 Jul 2;11(7):501-16. doi: 10.1080/15592294.2016.1184805. Epub 2016 May 31.

Abstract

Genomic imprinting is an epigenetic mechanism that leads to parental-allele-specific gene expression. Approximately 150 imprinted genes have been identified in humans and mice but less than 30 have been described as imprinted in cattle. For the purpose of de novo identification of imprinted genes in bovine, we determined global monoallelic gene expression in brain, skeletal muscle, liver, kidney and placenta of day ∼105 Bos taurus indicus × Bos taurus taurus F1 conceptuses using RNA sequencing. To accomplish this, we developed a bioinformatics pipeline to identify parent-specific single nucleotide polymorphism alleles after filtering adenosine to inosine (A-to-I) RNA editing sites. We identified 53 genes subject to monoallelic expression. Twenty three are genes known to be imprinted in the cow and an additional 7 have previously been characterized as imprinted in human and/or mouse that have not been reported as imprinted in cattle. Of the remaining 23 genes, we found that 10 are uncharacterized or unannotated transcripts located in known imprinted clusters, whereas the other 13 genes are distributed throughout the bovine genome and are not close to any known imprinted clusters. To exclude potential cis-eQTL effects on allele expression, we corroborated the parental specificity of monoallelic expression in day 86 Bos taurus taurus × Bos taurus taurus conceptuses and identified 8 novel bovine imprinted genes. Further, we identified 671 candidate A-to-I RNA editing sites and describe random X-inactivation in day 15 bovine extraembryonic membranes. Our results expand the imprinted gene list in bovine and demonstrate that monoallelic gene expression can be the result of cis-eQTL effects.

Keywords: A-to-I RNA editing; X chromosome inactivation; allele-specific gene expression; genomic imprinting; next generation sequencing.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Animals
  • Cattle / genetics*
  • Embryo, Mammalian / metabolism
  • Gene Expression Regulation, Developmental*
  • Genome*
  • Genomic Imprinting*
  • High-Throughput Nucleotide Sequencing
  • Polymorphism, Single Nucleotide
  • Quantitative Trait Loci*
  • RNA Editing
  • Sequence Analysis, DNA