Integrated analysis of mRNAs and long noncoding RNAs in the semen from Holstein bulls with high and low sperm motility

Xiuge Wang(Shandong Academy of Agricultural Sciences), Chunhong Yang(Shandong Academy of Agricultural Sciences), Fang Guo(Shandong Academy of Agricultural Sciences), Yaran Zhang(Shandong Academy of Agricultural Sciences), Zhihua Ju(Shandong Academy of Agricultural Sciences), Qiang Jiang(Shandong Academy of Agricultural Sciences), Xueming Zhao(Chinese Academy of Agricultural Sciences), Yong Liu(Shandong Academy of Agricultural Sciences), Han Zhao(Shandong Normal University), Jinpeng Wang(Shandong Academy of Agricultural Sciences), Yan Sun(Shandong Academy of Agricultural Sciences), Changfa Wang(Shandong Academy of Agricultural Sciences), Huabin Zhu(Chinese Academy of Agricultural Sciences), Jinming Huang(Shandong Normal University)
Scientific Reports
February 14, 2019
Cited by 63Open Access
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Abstract

Sperm motility is the main index used to assess the quality of bull semen. It may also be used to evaluate the fertility potential of bulls. Protein-coding mRNA and long noncoding RNA (lncRNA) participate in the regulation of spermatogenesis. Here, we employed strand-specific RNA sequencing to profile the semen transcriptome (mRNA and lncRNA) of six paired full-sibling Holstein bulls with divergent sperm motility and to determine the functions of mRNA and lncRNA in sperm motility. Among 20,875 protein-encoding genes detected in semen, 19 were differentially expressed between the high sperm motility group (H: H1, H2, and H3) and low sperm motility group (L: L1, L2, and L3). Of the 11,561 lncRNAs identified in sperm, 2,517 were differentially expressed between the H and L groups. We found that TCONS_00041733 lncRNA targets the node gene EFNA1 (ephrin A1), involved in male reproductive physiology. Our study provides a global mRNA and lncRNA transcriptome of bull semen, as well as novel insights into the regulation of neighboring protein coding by lncRNAs and the influence of mRNAs on sperm motility.


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