Abstract

BackgroundCryopreservation induces transcriptomic and epigenetic modifications that strongly impairs sperm quality and function, and thus decrease reproductive performance. N6-methyladenosine (m6A) RNA methylation varies in response to stress and has been implicated in multiple important biological processes, including post-transcriptional fate of mRNA, metabolism, and apoptosis. This study aimed to explore whether cryopreservation induces m6A modification of mRNAs associated with sperm energy metabolism, cryoinjuries, and freezability.ResultsThe mRNA and protein expression of m6A modification enzymes were significantly dysregulated in sperm after cryopreservation. Furthermore, m6A peaks were mainly enriched in coding regions and near stop codons with classical RRACH motifs. The mRNAs containing highly methylated m6A peaks (fts vs. fs) were significantly associated with metabolism and gene expression, while the genes with less methylated m6A peaks were primarily involved in processes regulating RNA metabolism and transcription. Furthermore, the joint analysis of DMMGs and differentially expressed genes indicated that both of these play a vital role in sperm energy metabolism and apoptosis.ConclusionsOur study is the first to reveal the dynamic m6A modification of mRNAs in boar sperm during cryopreservation. These epigenetic modifications may affect mRNA expression and are closely related to sperm motility, apoptosis, and metabolism, which will provide novel insights into understanding of the cryoinjuries or freezability of boar sperm during cryopreservation.

Highlights

  • Cryopreservation induces transcriptomic and epigenetic modifications that strongly impairs sperm quality and function, and decrease reproductive performance

  • We found highly diverse m6A patterns between fresh sperm (Fs) and frozenthawed sperm (Fts), and speculate that study of m6A modification patterns may present an opportunity to deepen our understanding of the role of epigenetic modifications in regulating sperm function during cryopreservation

  • The protein levels of methyltransferase-like 3 (METTL3), methyltransferaselike 14 (METTL14), and Fat mass and obesityassociated protein (FTO) were downregulated in response to cryopreservation (P < 0.01), whereas alkB homolog 5 (ALKBH5) and YTHDF2 were upregulated in the Fts group (P < 0.01, Fig. 1B C)

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Summary

Introduction

Cryopreservation induces transcriptomic and epigenetic modifications that strongly impairs sperm quality and function, and decrease reproductive performance. This study aimed to explore whether cryopreservation induces m6A modification of mRNAs associated with sperm energy metabolism, cryoinjuries, and freezability. Cryopreservation is a vital procedure with extensive applications for long-term semen storage, despite the associated risk for sperm cryoinjuries, including impaired motility, fertility, and apoptosis, due to oxidative stress [1,2,3,4]. The study of molecular markers and underlying mechanisms related to cold shock and freeze tolerance is imperative to improve AI outcomes. Sperm epigenetic markers, such as DNA methylation, histone modification, and non-coding RNAs are associated with successful fertilization and healthier offspring [8, 9].

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