Sarah E Wolf, Elizabeth M George, Jess Dong, Kimberly A Rosvall
{"title":"卵巢中端粒相关基因网络在环境因素中的变化。","authors":"Sarah E Wolf, Elizabeth M George, Jess Dong, Kimberly A Rosvall","doi":"10.1002/jez.70003","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":15711,"journal":{"name":"Journal of experimental zoology. Part A, Ecological and integrative physiology","volume":" ","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Telomere-Related Gene Networks in the Ovary Shift Across Environmental Factors.\",\"authors\":\"Sarah E Wolf, Elizabeth M George, Jess Dong, Kimberly A Rosvall\",\"doi\":\"10.1002/jez.70003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":15711,\"journal\":{\"name\":\"Journal of experimental zoology. Part A, Ecological and integrative physiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of experimental zoology. 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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.
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.