季节性热应激对安哥拉兔睾丸形态和转录组的负面影响。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Haisheng Ding, Yuanlang Wang, Huiling Zhao, Jinzi Wang, Dongwei Huang
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引用次数: 0

摘要

背景:暴露在高温条件下的睾丸温度会影响牲畜的繁殖性能。本研究旨在探讨安哥拉兔在春季(无热应激)、夏季(强热应激)和秋季(无热应激)三个季节睾丸精液质量、睾丸形态结构和基因表达谱的差异。结果:夏季热应激显著降低精液质量,损害睾丸形态和精子发生,秋季恢复到正常水平,但精液质量恢复明显缓慢。RNA-Seq分析显示,8703个基因在夏季表达水平发生显著变化,而在秋季表达水平恢复到春季水平,这与不同季节睾丸形态分析结果一致。富集分析显示,deg主要与精子发生、精子活力、精子发育、细胞死亡、凋亡过程的调节以及对外部刺激的反应有关。MAPK、Rap1、TNF、Ras、凋亡和Wnt信号通路调节热应激下的生殖。此外,在秋季和春季之间,睾丸形态和基因表达谱的变化很小。基因表达谱分析显示,夏季高表达基因主要参与细胞凋亡、免疫和热应激反应的调控,而夏季低表达基因主要参与精子发生的调控。结论:本研究考察了不同季节对雄性安哥拉兔生殖性能的影响,初步揭示了夏季睾丸对热应激反应的分子调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Negative effect of seasonal heat stress on testis morphology and transcriptomes in Angora rabbit.

Background: The temperature of testes exposed to hyperthermic conditions can affect livestock reproductive performance. This study aimed to explore the difference in semen quality, testicular morphological structure, and gene expression profiles of testes of Angora rabbits in spring (no heat stress), summer (intense heat stress), and autumn (no heat stress) seasons.

Results: Heat stress during summer significantly reduced semen quality and damaged testicular morphology and spermatogenesis, which recovered to normal levels in autumn, although semen quality recovery was notably slow. RNA-Seq analysis showed that the expression levels of 8703 genes changed significantly in summer, but their expression levels in autumn returned to those in spring, which was consistent with the testicular morphology analysis results in different seasons. Enrichment analysis revealed that the DEGs were primarily associated with spermatogenesis, sperm motility, spermatid development, cell death, regulation of apoptotic processes, and responses to external stimuli. The MAPK, Rap1, TNF, Ras, Apoptosis, and Wnt signaling pathways regulated reproduction under heat stress. In addition, minimal variations in testicular morphology and gene expression profiles were observed between autumn and spring. Gene expression pattern analysis showed that genes with high expression in summer mainly participated in the regulation of cell apoptosis, immunity, and response to heat stress, whereas genes with low expression in summer mainly participated in the regulation of spermatogenesis.

Conclusions: This study investigated the influence of different seasons on the reproductive performance of male Angora rabbits and provided initial insights into the molecular regulatory mechanisms underlying the testicular response to heat stress during summer.

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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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