Promoter hypermethylation of PIWI/piRNA pathway genes associated with diminished pachytene piRNA production in bovine hybrid male sterility

Epigenetics. 2020 Sep;15(9):914-931. doi: 10.1080/15592294.2020.1738026. Epub 2020 Mar 6.

Abstract

Hybrid male sterility (HMS) is a postzygotic reproductive isolation mechanism that enforces speciation. A bovine example of HMS is the yattle (also called dzo), an interspecies hybrid of taurine cattle (Bos taurus) and yak (Bos grunniens). The molecular mechanisms underlying HMS of yattle are not well understood. Epigenetic modifications of DNA methylation and P-element induced wimpy testis (PIWI)-interacting RNA (piRNAs) are important regulators in spermatogenesis. In this study, we investigated DNA methylation patterns and piRNA expression in adult testes in hybrid infertile yattle bulls and fertile cattle and yak bulls using whole genome bisulphite-seq and small RNA-seq. Promoter hypermethylation in yattle were associated with DNA methylation involved in gamete generation, piRNA metabolic processes, spermatogenesis, and spermatid development (P < 2.6 × 10-5). Male infertility in yattle was associated with the promoter hypermethylation-associated silencing of PIWI/piRNA pathway genes including PIWIL1, DDX4, PLD6, MAEL, FKBP6, TDRD1 and TDRD5. The downstream effects of silencing these genes were diminished production of 29- to 31- nucleotide pachytene piRNAs in yattle testes. Hypermethylation events at transposable element loci (LINEs, SINEs, and LTRs) were found in yattle. LINE-derived prepachytene piRNAs increased and SINE-derived prepachytene piRNAs were reduced in yattle testes. Our data suggests that DNA methylation affects the PIWI/piRNA pathway and is involved in gene expression and pachytene piRNA production during spermatogenesis in bovine HMS. DNA hypermethylation and disruption of piRNA production contributed to unsuccessful germ cell development that may drive bovine HMS.

Keywords: DNA methylation; Hybrid male sterility; piRNA biogenesis; transposon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Argonaute Proteins / genetics
  • Argonaute Proteins / metabolism
  • Cattle / genetics*
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • DNA Methylation*
  • Infertility, Male / genetics*
  • Infertility, Male / veterinary
  • Long Interspersed Nucleotide Elements
  • Male
  • Pachytene Stage*
  • Promoter Regions, Genetic
  • RNA, Small Interfering / genetics*
  • RNA, Small Interfering / metabolism
  • Spermatogenesis
  • Testis / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Argonaute Proteins
  • Cell Cycle Proteins
  • RNA, Small Interfering
  • Transcription Factors

Grants and funding

This work was financially supported by the National Natural Science Foundation of China [grant no. 31802046] and the Chongqing Research Program of Basic Research and Frontier Technology [cstc2017jcyjBX0013 and cstc2018jcyjAX0524] and Fundamental Research Funds for the Central Universities [XDJK2019RC001]. The funders had no role in study design, decision to publish, or preparation of the manuscript.