Evidence map›Paper›PMID 42518043›Full record

ArticleScience China. Life sciences2026

Cross-species comparative transcriptomic analysis of spermatozoa reveals species-specific regulatory networks linked to fertilization-associated genes in cattle, sheep and goats.

Yue Zhao, Linfeng Bai, Qiqi Jiang, Hao Xiao, Fangyuan Liu, Bilige Wuyun, Rihan Wu, Chunxia Hao, Rui Ding, Peng Yuan and 6 more

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Article in Science China. Life sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Yue Zhao *State Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Linfeng Bai *State Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Qiqi JiangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Hao XiaoState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Fangyuan LiuState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Bilige WuyunState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Rihan WuState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Chunxia HaoState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Rui DingInner Mongolia SaiKexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Peng YuanInner Mongolia SaiKexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Lizhi WangInner Mongolia SaiKexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Ying LuCollege of Fisheries and Life Science, Shanghai Ocean University, Shanghai, 201306, China.
Qingyuan SunFertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou, 510403, China.
Zhigang WangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.
Yongli SongState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China. ylsong@imu.edu.cn.
Xihe LiState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, 010070, China. lixh@imu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian sperm RNAs, encompassing coding and non-coding sequences, have historically been considered residual by-products of spermatogenesis. However, accumulating evidence has revealed that mature sperm-derived RNAs not only participate in zygote formation and embryonic cleavage but also exhibit multifaceted biological functions. Notably, interspecies variations in sperm transcriptomic profiles among cattle, sheep, and goats, particularly those linked to species-specific regulatory networks with fertilization-associated genes, remain underexplored. This study systematically characterized mRNAs, miRNAs, and circRNAs components within sperm transcriptomes across these three ruminant species, with comparative analysis of interspecies divergence. High-throughput sequencing identified distinct RNA repertoires: cattle sperm contained 15,661 mRNAs, 442 miRNAs, and 3,358 circRNAs; sheep sperm comprised 13,883 mRNAs, 474 miRNAs, and 3,449 circRNAs; goat sperm exhibited 15,725 mRNAs, 588 miRNAs, and 5,081 circRNAs. Cross-species comparisons revealed that 5,782 differentially expressed mRNAs, 11 differentially expressed miRNAs, and 60 differentially expressed circRNAs were shared by the three species, alongside species-unique gene clusters. A competitive endogenous RNAs (ceRNA) network integrating mRNAs, miRNAs, and circRNAs was constructed, and species-specific regulatory networks associated with fertilization were identified, including circMEMOl-bta-miR-497-IZUMO4, circAKT2-novel-bta-miR433-3p-CATSPERD, circFBXW7-novel-bta-miR382-3p-CATSPER2, circSTAU1-novel-oar-miR1301-5p-PRM3, and circJMJD1C-novel-chi-miR2159-3p-IZUMO2. This study demonstrates the interspecies divergences in sperm transcriptomic profiles and regulatory networks among cattle, sheep, and goats, establishing a novel research paradigm centered on 'coding & non-coding RNAs interplay' in mammalian sperm transcriptomic regulation, and thereby providing a generalizable systematic analytical tool for deciphering complex reproductive biological processes.

Indexed as

cattleceRNA networkcross-species analysisgoatsheepsperm whole-transcriptome

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.