Tigriopus californicus 的 F1 代杂交种在耐缺氧性方面缺乏异质性。

IF 3 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Aimee Deconinck, Olivia Madalone, Chris Willett
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引用次数: 0

摘要

杂交会产生从有利到不利的一系列结果,而基因研究的一个目标就是了解产生这些结果的基因相互作用。线粒体等细胞质元素与细胞核之间的相互作用,由于进化速度不同,可能特别容易产生不利组合。然而,线粒体与细胞核之间的不相容性往往要到 F2 代及以后几代才会产生明显的影响。我们利用有丝分裂核互不相容的模式系统加利福尼亚褐虎(Tigriopus californicus)来测试缺氧是否比其他环境胁迫因素对有丝分裂核相互作用造成更大的胁迫。我们从四个群体杂交中产生了 284 个亲本和 436 个 F1 杂交种(共 720 个),并比较了亲本和 F1 群体对低氧的耐受性。我们观察到,平均而言,与亲本相比,F1 杂交种在低氧胁迫测试中存活的可能性较低(亲本:F1 系数从-0.04 到 0.14 不等,无显著差异)。这表明缺氧对有丝分裂核协调可能是一种特别强烈的压力,杂交结果因性状而异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absence of heterosis for hypoxia tolerance in F1 hybrids of Tigriopus californicus.

Hybridization produces a range of outcomes from advantageous to disadvantageous, and a goal of genetic research is to understand the gene interactions that generate these outcomes. Interactions between cytoplasmic elements, such as mitochondria, and the nucleus may be particularly vulnerable to accruing disadvantageous combinations as a result of their different rates of evolution. However, mitonuclear incompatibilities often do not have an observable effect until the F2 and later generations. We used Tigriopus californicus, a model system for mitonuclear incompatibilities that is also known for exhibiting heterosis in the F1 generation, to test whether hypoxia was more stressful for mitonuclear interactions than other environmental stressors. We generated 284 parental and 436 F1 hybrids from four population crosses (720 total) and compared parental and F1 populations for hypoxia tolerance. We observed that, on average, F1 hybrids were less likely to survive a hypoxia stress test than parental populations (Parental:F1 coefficients ranged from -0.04 to 0.14 with none significantly different from 0). This suggests that hypoxia may be a particularly intense stressor for mitonuclear coordination, and that hybridization outcomes vary by trait.

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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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