发情周期山羊不同生殖力子宫相关环状rna的鉴定及表达谱分析。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Xiaolong Du, Yufang Liu, Xiaoyun He, Lin Tao, Meiying Fang, Mingxing Chu
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引用次数: 0

摘要

背景:云上黑山羊是中国著名的肉用山羊品种,以其优越的繁殖能力而闻名。尽管如此,品种内仍有相当大的表型变异性。在生殖周期中,子宫起着举足轻重的作用,其功能随着周期的不同阶段而变化。本研究以高繁殖力(HF)和低繁殖力(LF)云上黑山羊在发情周期的增殖期(FP)和分泌期(LP)的子宫组织为研究对象,包括子宫内膜和子宫肌层。通过检查这些组织,我们旨在阐明观察到的生殖成功差异的潜在分子和生理机制。结果:进行了高通量测序,然后进行了生物信息学分析,确定了circRNAs的表达谱。通过整合find_circ和CIRI2软件的发现,共鉴定出7445个circrna。FPLF与FPHF、LPLF与LPHF的比较分析显示,分别有149个差异表达(DE)环状rna(94个上调,55个下调)和276个DE环状rna(56个上调,220个下调)。富集分析表明,参与的主要通路为鞘脂信号通路、MAPK信号通路和GnRH信号通路,它们都与细胞生长发育密切相关。此外,还鉴定了几个关键的候选基因,如FGF2和MBTPS1。我们还预测了总共281个miRNA-circRNA结合对,包括263个circrna和60个mirna,同时预测了14个编码circrna。结论:在此基础上,我们分别建立了卵泡期和黄体期circRNAs的表达谱。此外,利用各种分析方法和来自不同时期高产和低产量实验对照组的数据,我们已经确定了影响山羊高繁殖能力的多个环状rna。通过对这些环状rna宿主基因的富集分析,我们发现了几个关键的候选基因。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification and expression profile analysis of circRNAs associated with goat uterus with different fecundity during estrous cycle.

Background: 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.

Results: 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.

Conclusion: 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.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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