Du Xiaolong, Liu Yufang, He Xiaoyun, Tao Lin, Fang Meiying, Chu Mingxing
State Key Laboratory of Animal Biotech Breeding, Institute of Animal Science, Chinese Academy of Agricultural Sciences (CAAS), Beijing, 100193, China.
Department of Animal Genetics and Breeding, Laboratory of Animal Genetics and Breeding, College of Animal Science and Technology, National Engineering Laboratory for Animal Breeding, MARA, China Agricultural University, Beijing, 100193, China.
BMC Genomics. 2025 Apr 7;26(1):349. doi: 10.1186/s12864-025-11489-x.
The Yunshang Black Goat, a distinguished meat goat breed native to China, is renowned for its superior reproductive capabilities. Despite this, there is considerable phenotypic variability within the breed. During the reproductive cycle, the uterus plays a pivotal role, with its functions evolving in line with the different stages of the cycle. This study focuses on the uterine tissues, including both the endometrium and myometrium, of Yunshang Black Goats with high fecundity (HF) and low fecundity (LF) during the proliferative (FP) and secretory (LP) phases of the estrous cycle. By examining these tissues, we aim to elucidate the underlying molecular and physiological mechanisms of the observed differences in reproductive success.
High-throughput sequencing was conducted, followed by bioinformatics analysis to identify the expression profiles of circRNAs. A total of 7,445 circRNAs were identified through the integration of findings from find_circ and CIRI2 software. Comparative analyses between the FPLF vs. FPHF and LPLF vs. LPHF revealed 149 differentially expressed (DE) circRNAs (94 up-regulated and 55 down-regulated) and 276 DE circRNAs (56 up-regulated and 220 down-regulated), respectively. The enrichment analysis indicated that the primary pathways involved were the Sphingolipid signaling pathway, MAPK signaling pathway, and GnRH signaling pathway, all of which are closely associated with cellular growth and development. Additionally, several key candidate genes were identified, such as FGF2 and MBTPS1. We also predicted a total of 281 miRNA-circRNA binding pairs, encompassing 263 circRNAs and 60 miRNAs, and simultaneously, 14 coding circRNAs were anticipated.
Based on the analysis, we have established the expression profiles of circRNAs during the follicular and luteal phases, respectively. Furthermore, using various analytical methods and data from high- and low-yield experimental control groups over different periods, we have identified multiple circRNAs that affect the high reproductive capacity of goats. Through enrichment analysis of the host genes of these circRNAs, we have discovered several key candidate genes. These findings provide fundamental data for the study of the molecular mechanisms underlying the fecundity of goats and pave the way for future genetic improvement strategies.
云上黑山羊是中国特有的优良肉用山羊品种,以其卓越的繁殖能力而闻名。尽管如此,该品种内仍存在相当大的表型变异。在生殖周期中,子宫起着关键作用,其功能随着周期的不同阶段而演变。本研究聚焦于发情周期增殖期(FP)和分泌期(LP)高繁殖力(HF)和低繁殖力(LF)的云上黑山羊的子宫组织,包括子宫内膜和肌层。通过对这些组织的研究,我们旨在阐明观察到的繁殖成功率差异背后的分子和生理机制。
进行了高通量测序,随后进行生物信息学分析以确定环状RNA(circRNA)的表达谱。通过整合find_circ和CIRI2软件的结果,共鉴定出7445个circRNA。FPLF与FPHF以及LPLF与LPHF之间的比较分析分别揭示了149个差异表达(DE)的circRNA(94个上调和55个下调)和276个DE circRNA(56个上调和220个下调)。富集分析表明,主要涉及的途径是鞘脂信号通路、丝裂原活化蛋白激酶(MAPK)信号通路和促性腺激素释放激素(GnRH)信号通路,所有这些都与细胞生长和发育密切相关。此外,还鉴定了几个关键候选基因,如成纤维细胞生长因子2(FGF2)和膜内蛋白酶位点1(MBTPS1)。我们还总共预测了281个miRNA-circRNA结合对,包括263个circRNA和60个miRNA,同时,预计有14个编码circRNA。
基于分析,我们分别建立了卵泡期和黄体期circRNA的表达谱。此外,利用不同时期高产和低产实验对照组的各种分析方法和数据,我们鉴定了多个影响山羊高繁殖力的circRNA。通过对这些circRNA宿主基因的富集分析,我们发现了几个关键候选基因。这些发现为研究山羊繁殖力的分子机制提供了基础数据,并为未来的遗传改良策略铺平了道路。