MHC II 类超型影响迁徙鸣禽的存活率和终生繁殖成功率。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
David Canal, Jacob Roved, Antonio Lara, Carlos Camacho, Jaime Potti, Simone Santoro
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引用次数: 0

摘要

主要组织相容性复合体(MHC)在针对病原体的免疫反应中发挥着关键作用。它的高度多态性被认为主要是宿主-病原体共同进化的结果,但对于自然种群来说,阐明驱动 MHC 进化的机制仍然具有挑战性。我们调查了斑鹊Ficedula hypoleuca野生种群中MHC II类基因的多样性,并测试了其与个体适应性的两个关键组成部分:终生繁殖成功率和存活率的关系。在研究种群的 180 只繁殖成鸟中,我们发现了 182 个独特的 MHC II 外显子 2 等位基因。这些等位基因显示出强烈的正选择信号,并根据推断出的抗原结合位点的理化特性分为九个功能超型。在超过 98% 的采样个体中发现了三种超类型,这表明它们在人群中几乎是固定的。我们在人群中没有发现罕见的超级类型,因为所有超级类型在大于 70% 的个体中都存在。三种超级类型与个体适应性的不同组成部分有关:其中两种与随时间推移后代产量降低有关,而第三种则与存活率呈正相关。总体而言,大量等位基因和功能多样性以及特定超级类型与适应性之间的关系符合平衡选择维持研究人群中 MHC II 类多样性的观点,可能波动选择是其基本机制。种群中不存在稀有超型,这表明平衡选择不是由稀有等位基因优势驱动的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MHC Class II Supertypes Affect Survival and Lifetime Reproductive Success in a Migratory Songbird

MHC Class II Supertypes Affect Survival and Lifetime Reproductive Success in a Migratory Songbird

The major histocompatibility complex (MHC) plays a critical role in the immune response against pathogens. Its high polymorphism is thought to be mainly the consequence of host-pathogen co-evolution, but elucidating the mechanism(s) driving MHC evolution remains challenging for natural populations. We investigated the diversity of MHC class II genes in a wild population of pied flycatchers Ficedula hypoleuca and tested its associations with two key components of individual fitness: lifetime reproductive success and survival. Among 180 breeding adults in our study population, we found 182 unique MHC class II exon 2 alleles. The alleles showed a strong signal of positive selection and grouped into nine functional supertypes based on physicochemical properties at the inferred antigen-binding sites. Three supertypes were found in > 98% of the sampled individuals, indicating that they are nearly fixed in the population. We found no rare supertypes in the population, as all supertypes were present in > 70% of individuals. Three supertypes were related to different components of individual fitness: two were associated with lower offspring production over time, while the third was positively associated with survival. Overall, the substantial allelic and functional diversity and the relationship between specific supertypes and fitness are in accordance with the notion that balancing selection maintains MHC class II diversity in the study population, possibly with fluctuating selection as the underlying mechanism. The absence of rare supertypes in the population suggests that the balancing selection is not driven by rare-allele advantage.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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