全基因组时间基因表达揭示了线虫C. briggsae的生殖后转移。

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Wouter van den Berg, Bhagwati P Gupta
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引用次数: 0

摘要

秀丽隐杆线虫及其著名的表亲秀丽隐杆线虫为影响生理过程的遗传途径的比较研究提供了许多特征。生殖就是这样一个直接影响寿命的过程,因为它需要大量的能量。为了研究这两种线虫在生殖和生殖后阶段的基因表达变化,我们在不同的成虫阶段进行了全基因组转录组分析。结果表明,两个物种的大部分差异表达(DE)基因在繁殖期间下调。有趣的是,在C. briggsae中,这种趋势在繁殖后发生逆转,四分之三的DE基因变得上调。另一小部分DE基因则呈现相反的表达趋势,即先上调后生殖后下调。总的来说,我们把这种现象称为“后生育转变”。相比之下,生殖后的转变在秀丽隐杆线虫中就不那么明显了。在C. briggsae中,DE基因在生殖期与基质、肌肉发育和功能相关的过程中富集。生殖后下调基因在DNA损伤修复、应激反应和免疫反应中富集。此外,与脂肪酸代谢、分解代谢和转录调控相关的术语表现出复杂的模式。通过实验操作来影响C. briggsae的生殖状态,可预测地改变了基因表达,为生殖后转变提供了体内支持。总的来说,我们的研究揭示了C. briggsae在生殖和生殖后变化过程中新的基因表达模式。这些数据为线虫和其他动物模型的横断面比较研究提供了宝贵的资源,以了解影响生殖和衰老的遗传途径的进化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome-Wide Temporal Gene Expression Reveals a Post-Reproductive Shift in the Nematode Caenorhabditis briggsae.

The nematodes Caenorhabditis briggsae and its well-known cousin Caenorhabditis elegans offer many features for comparative investigations of genetic pathways that affect physiological processes. Reproduction is one such process that directly impacts longevity due to its significant energetic demands. To study gene expression changes during reproductive and post-reproductive phases in both these nematodes, we conducted whole-genome transcriptome profiling at various adult stages. The results revealed that the majority of differentially expressed (DE) genes were downregulated during the reproductive period in both species. Interestingly, in C. briggsae, this trend reversed during post-reproduction, with three-quarters of the DE genes becoming upregulated. Additionally, a smaller set of DE genes showed an opposite expression trend, i.e. upregulation followed by post-reproductive downregulation. Overall, we termed this phenomenon the "post-reproductive shift". In contrast, the post-reproductive shift was much less pronounced in C. elegans. In C. briggsae, DE genes were enriched in processes related to the matrisome, muscle development and function during the reproductive period. Post-reproductive downregulated genes were enriched in DNA damage repair, stress response, and immune response. Additionally, terms related to fatty acid metabolism, catabolism, and transcriptional regulation exhibited complex patterns. Experimental manipulations in C. briggsae to affect their reproductive status predictably altered gene expression, providing in vivo support for the post-reproductive shift. Overall, our study reveals novel gene expression patterns during reproductive and post-reproductive changes in C. briggsae. The data provide a valuable resource for cross-sectional comparative studies in nematodes and other animal models to understand evolution of genetic pathways affecting reproduction and aging.

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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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