卵巢中端粒相关基因网络在环境因素中的变化。

IF 1.9 3区 生物学 Q1 ZOOLOGY
Sarah E Wolf, Elizabeth M George, Jess Dong, Kimberly A Rosvall
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引用次数: 0

摘要

卵巢是将环境因素与后代发育的时间和质量联系起来的关键。以自由生活的雌性树燕(Tachycineta bicolor)为研究对象,我们测量了参与端粒长度调节的基因在卵巢表达的时间变化。使用qPCR,我们定量了庇护蛋白(TERF1, TERF2, TERF2IP, TPP1, POT1),端粒酶(TERT),抗氧化剂(SOD1, PRDX-1, GPX)和糖皮质激素受体(MR, GR)的mRNA丰度。我们询问了它们在繁殖阶段和社会环境中的差异,然后我们评估了基因共表达的影响,这反映了相互作用基因网络中的协调变化。我们假设端粒的维持在繁殖过程中,即在产卵之前和在社会挑战之后,被上调和更强烈地协同调节。我们没有发现环境背景对mRNA丰度的主要影响,但我们确实发现了基因共表达网络的细微差异。雌性在孵育过程中表现出更强的庇护蛋白间的协同调节和与糖皮质激素受体间更强的串扰。在面对同种挑战时,抗氧化剂与庇护素和糖皮质激素受体的协同调节较弱或呈负相关,表明这些端粒调节网络具有半独立的社会调节作用。虽然这些转录差异的后果需要更多的研究,但我们的研究结果表明,环境可能有助于保护卵巢,包括其端粒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Telomere-Related Gene Networks in the Ovary Shift Across Environmental Factors.

The ovary is key to linking environmental factors with the timing and quality of offspring development. Focused on free-living female tree swallows (Tachycineta bicolor), we measured temporal variation in ovarian expression of genes involved in the regulation of telomere length. Using qPCR, we quantified mRNA abundance of shelterin proteins (TERF1, TERF2, TERF2IP, TPP1, POT1), telomerase (TERT), antioxidants (SOD1, PRDX-1, GPX), and glucocorticoid receptors (MR, GR). We asked how they differ across breeding stages and social environments, and then we assessed effects on gene co-expression, which reflects coordinated changes across this network of interacting genes. We hypothesized that maintenance of telomeres is upregulated and more strongly coregulated in the lead up to reproduction, i.e., before egg-laying and following a social challenge. We did not find a main effect of environmental context on mRNA abundance, but we did detect subtle differences in gene co-expression networks. Females exhibited stronger coregulation among shelterin proteins and stronger crosstalk with glucocorticoid receptors during incubation. In response to a conspecific challenger, coregulation of antioxidants with shelterin and glucocorticoid receptors was weaker or more negatively correlated, suggesting semi-independent social modulation of these telomere regulatory networks. While the consequences of these transcriptional differences require more research, our results suggest that the environment could contribute to protection of the ovary, including its telomeres.

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来源期刊
Journal of experimental zoology. Part A, Ecological and integrative physiology
Journal of experimental zoology. Part A, Ecological and integrative physiology Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
4.90
自引率
3.60%
发文量
0
期刊介绍: The Journal of Experimental Zoology – A publishes articles at the interface between Development, Physiology, Ecology and Evolution. Contributions that help to reveal how molecular, functional and ecological variation relate to one another are particularly welcome. The Journal publishes original research in the form of rapid communications or regular research articles, as well as perspectives and reviews on topics pertaining to the scope of the Journal. Acceptable articles are limited to studies on animals.
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