Ex situ reared black-footed ferrets exhibit altered sperm DNA methylation.

IF 2.5 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Alexandra L DeCandia, Stavi R Tennenbaum, Rachel Santymire, Travis Livieri, Robyn Bortner, Della Garelle, Adrienne Crosier, Paul Marinari, Budhan S Pukazhenthi, Pierre Comizzoli, Jesús E Maldonado, Klaus-Peter Koepfli, Bridgett M vonHoldt
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引用次数: 0

Abstract

Many endangered species rely on ex situ management for survival when external threats exist on the landscape. Yet ex situ settings pose challenges through space limitation, altered environment, and diet. This can lead to environmentally-determined inbreeding depression, where ex situ animals exhibit reduced reproductive fitness compared to their in situ counterparts, despite originating from the same genetic stock. We investigated epigenetic differences as a potential mechanism underlying environmentally-determined inbreeding depression in black-footed ferrets (Mustela nigripes), an North American endemic species reliant on ex situ conservation. More specifically, we explored how environmental context may influence sperm DNA methylation in samples collected from 12 ex situ and 5 in situ males. Average sperm DNA methylation was significantly higher in ex situ individuals. We additionally identified >500 differentially methylated regions between ex situ and in situ sperm samples that were enriched for gene ontology terms pertaining to reproduction and development. Putative genes of interest included NPR2, WEE2, SLC15A1, PDE10A, PIP5K1B, CACNA1E, and CACNA1A, all of which have previously been linked to spermatogenesis, sperm motility, or fertilization in mammals. Results suggest that environmental conditions may alter sperm DNA methylation in black-footed ferrets, with possible links to decreased reproductive success in ex situ settings. These findings provide valuable insights to the molecular mechanisms underlying environmentally-determined inbreeding depression in black-footed ferrets and other conservation-reliant species, and can serve as a foundation for future research on improving reproductive health in endangered wildlife.

非原位饲养的黑足雪貂表现出精子DNA甲基化的改变。
当景观受到外部威胁时,许多濒危物种依靠迁地管理生存。然而,通过空间限制、环境改变和饮食,迁地设置带来了挑战。这可能导致由环境决定的近亲繁殖衰退,尽管来自相同的遗传种群,但与原位动物相比,非原位动物表现出更低的生殖适应性。我们研究了黑足雪貂(Mustela nigripes)的表观遗传差异作为环境决定近交抑制的潜在机制,黑足雪貂是一种依赖于迁地保护的北美特有物种。更具体地说,我们探讨了环境背景如何影响从12个非原位和5个原位男性收集的样本中的精子DNA甲基化。非原位个体的平均精子DNA甲基化明显更高。此外,我们在非原位和原位精子样本之间发现了bb500000个差异甲基化区域,这些区域丰富了与生殖和发育有关的基因本体术语。推测的相关基因包括NPR2、WEE2、SLC15A1、PDE10A、PIP5K1B、CACNA1E和CACNA1A,所有这些基因之前都被认为与哺乳动物的精子发生、精子活力或受精有关。结果表明,环境条件可能会改变黑足雪貂的精子DNA甲基化,这可能与非原位环境下繁殖成功率降低有关。这些发现为研究环境决定的黑足雪貂和其他依赖保护的物种近亲繁殖抑制的分子机制提供了有价值的见解,并可为未来改善濒危野生动物生殖健康的研究奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Heredity
Journal of Heredity 生物-遗传学
CiteScore
5.20
自引率
6.50%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Over the last 100 years, the Journal of Heredity has established and maintained a tradition of scholarly excellence in the publication of genetics research. Virtually every major figure in the field has contributed to the journal. Established in 1903, Journal of Heredity covers organismal genetics across a wide range of disciplines and taxa. Articles include such rapidly advancing fields as conservation genetics of endangered species, population structure and phylogeography, molecular evolution and speciation, molecular genetics of disease resistance in plants and animals, genetic biodiversity and relevant computer programs.
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