调控区域的差异和基因复制可能是沙漠象龟时间生物学适应的基础。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
N. Jade Mellor, Timothy H. Webster, Hazel Byrne, Avery S. Williams, Taylor Edwards, Dale F. DeNardo, Melissa A. Wilson, Kenro Kusumi, Greer A. Dolby
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引用次数: 0

摘要

许多细胞过程和有机体行为是时间依赖的,这些现象的异步性可以通过强化机制促进物种形成。莫哈韦沙漠象龟和索诺兰沙漠象龟(分别为Gopherus agassizii和G. morafkai)生活在具有不同季节性降雨模式的相邻沙漠中,它们表现出不同步的冬季繁殖和繁殖行为。我们使用了来自两种陆龟和一个外群的21个个体的全基因组测序来了解这些特征的潜在基因。在基因组中分化程度最高的1% (FST≥0.63)中,假设存在功能变异的基因在调控元件,特别是启动子区域上表现出广泛的分化。这些基因与紫外线核苷酸切除、修复、有丝核和体内平衡功能有关。介导时间生物学(细胞周期、昼夜节律和周期)过程的基因也在分化程度最高的区域(如XPA和ZFHX3)。假设的启动子变异显著富集了与调控机制相关的基因(ARC-Mediator complex),这表明由调控差异驱动的转录级联反应可能是这些物种之间行为差异的基础,导致了基于异步的前合子分离。进一步的研究表明,在地鼠体内,特别是莫拉凯地鼠体内,呼吸和肠粘蛋白(MUC5B和MUC5AC)广泛扩增。这种扩张可能是对水分保持的干旱适应和/或导致两个物种之间阿加西支原体感染率的差异,因为粘蛋白有助于清除吸入的灰尘和细菌。总体而言,研究结果强调了物种形成过程中存在的多样性遗传变化,包括分化、适应和强化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Divergence in Regulatory Regions and Gene Duplications May Underlie Chronobiological Adaptation in Desert Tortoises

Many cellular processes and organismal behaviours are time-dependent, and asynchrony of these phenomena can facilitate speciation through reinforcement mechanisms. The Mojave and Sonoran desert tortoises (Gopherus agassizii and G. morafkai respectively) reside in adjoining deserts with distinct seasonal rainfall patterns and they exhibit asynchronous winter brumation and reproductive behaviours. We used whole genome sequencing of 21 individuals from the two tortoise species and an outgroup to understand genes potentially underlying these characteristics. Genes within the most diverged 1% of the genome (FST ≥ 0.63) with putatively functional variation showed extensive divergence in regulatory elements, particularly promoter regions. Such genes related to UV nucleotide excision repair, mitonuclear and homeostasis functions. Genes mediating chronobiological (cell cycle, circadian and circannual) processes were also among the most highly diverged regions (e.g., XPA and ZFHX3). Putative promoter variants had significant enrichment of genes related to regulatory machinery (ARC-Mediator complex), suggesting that transcriptional cascades driven by regulatory divergence may underlie the behavioural differences between these species, leading to asynchrony-based prezygotic isolation. Further investigation revealed extensive expansion of respiratory and intestinal mucins (MUC5B and MUC5AC) within Gopherus, particularly G. morafkai. This expansion could be a xeric-adaptation to water retention and/or contribute to differential Mycoplasma agassizii infection rates between the two species, as mucins help clear inhaled dust and bacterial. Overall, results highlight the diverse array of genetic changes underlying divergence, adaptation and reinforcement during speciation.

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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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