基因和端粒的变异性:热带禽类杂交区的启示。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ben J. Vernasco, Kira M. Long, Michael J. Braun, Jeffrey D. Brawn
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引用次数: 0

摘要

端粒长度和端粒动态可与寿命、行为和个体素质相关联。这种关系激发了人们对了解人群内部和人群之间端粒长度及其动态变化的兴趣。许多研究已经确定了环境过程如何影响端粒动态,但遗传变异的作用还不太清楚。为了提供端粒变异与遗传变异之间关系的新视角,我们在一个狭窄的杂交区(n = 127个样本)内对个体进行了纵向采样,在该杂交区内有两个以全基因组杂合度对比为特征的马纳库斯物种进行杂交。我们测量了个体(n = 66)和种群(n = 3)全基因组杂合度的差异,并利用 RADseq 生成的 SNP 测量了杂交种之间的遗传混杂量。我们检测了端粒长度和端粒动态的种群差异。然后,我们研究了端粒长度和端粒动态与种群内全基因组杂合度的协整关系。与相邻亲本种群的个体相比,杂交个体的端粒平均较长。在端粒动态方面没有观察到种群差异。在杂合度相对较低的亲本种群中,较高的全基因组杂合度与较短的端粒和较高的端粒缩短率相关--这种模式在其他种群中不太明显。尽管雌雄人面鸟的生活史截然不同,但所有这些关系都与性别无关。我们的研究强调了种群比较如何揭示遗传变异和端粒之间的相互关系,以及自然发生的杂交和全基因组杂合度如何与端粒长度和端粒动态相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genetic and telomeric variability: Insights from a tropical avian hybrid zone

Genetic and telomeric variability: Insights from a tropical avian hybrid zone

Telomere lengths and telomere dynamics can correlate with lifespan, behaviour and individual quality. Such relationships have spurred interest in understanding variation in telomere lengths and their dynamics within and between populations. Many studies have identified how environmental processes can influence telomere dynamics, but the role of genetic variation is much less well characterized. To provide a novel perspective on how telomeric variation relates to genetic variability, we longitudinally sampled individuals across a narrow hybrid zone (n = 127 samples), wherein two Manacus species characterized by contrasting genome-wide heterozygosity interbreed. We measured individual (n = 66) and population (n = 3) differences in genome-wide heterozygosity and, among hybrids, amount of genetic admixture using RADseq-generated SNPs. We tested for population differences in telomere lengths and telomere dynamics. We then examined how telomere lengths and telomere dynamics covaried with genome-wide heterozygosity within populations. Hybrid individuals exhibited longer telomeres, on average, than individuals sampled in the adjacent parental populations. No population differences in telomere dynamics were observed. Within the parental population characterized by relatively low heterozygosity, higher genome-wide heterozygosity was associated with shorter telomeres and higher rates of telomere shortening—a pattern that was less apparent in the other populations. All of these relationships were independent of sex, despite the contrasting life histories of male and female manakins. Our study highlights how population comparisons can reveal interrelationships between genetic variation and telomeres, and how naturally occurring hybridization and genome-wide heterozygosity can relate to telomere lengths and telomere dynamics.

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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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