Signatures of Adaptation and Purifying Selection in Highland Populations of Dasiphora fruticosa.

IF 11 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fu-Sheng Yang, Min Liu, Xing Guo, Chao Xu, Juan Jiang, Weixue Mu, Dongming Fang, Yong-Chao Xu, Fu-Min Zhang, Ying-Hui Wang, Ting Yang, Hongyun Chen, Sunil Kumar Sahu, Ruirui Li, Guanlong Wang, Qiang Wang, Xun Xu, Song Ge, Huan Liu, Ya-Long Guo
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Abstract

High mountains harbor a considerable proportion of biodiversity, but we know little about how diverse plants adapt to the harsh environment. Here we finished a high-quality genome assembly for Dasiphora fruticosa, an ecologically important plant distributed in the Qinghai-Tibetan Plateau and lowland of the Northern Hemisphere, and resequenced 592 natural individuals to address how this horticulture plant adapts to highland. Demographic analysis revealed D. fruticosa underwent a bottleneck after Naynayxungla Glaciation. Selective sweep analysis of two pairs of lowland and highland populations identified 63 shared genes related to cell wall organization or biogenesis, cellular component organization, and dwarfism, suggesting parallel adaptation to highland habitats. Most importantly, we found that stronger purging of estimated genetic load due to inbreeding in highland populations apparently contributed to their adaptation to the highest mountain. Our results revealed how plants could tolerate the extreme plateau, which could provide potential insights for species conservation and crop breeding.

Dasiphora fruticosa高原种群的适应和净化选择特征。
高山蕴藏着相当大比例的生物多样性,但我们对多种植物如何适应严酷的环境知之甚少。在这里,我们完成了分布于青藏高原和北半球低地的重要生态植物Dasiphora fruticosa的高质量基因组组装,并对592个自然个体进行了重新测序,以探讨这种园艺植物如何适应高原环境。人口统计学分析表明,D. fruticosa在纳雍格拉冰川期后经历了一个瓶颈期。对两对低地和高地种群的选择性扫描分析发现了 63 个与细胞壁组织或生物发生、细胞组分组织和矮化有关的共享基因,这表明它们对高地生境的适应是平行的。最重要的是,我们发现高地种群对近亲繁殖造成的估计遗传负荷进行了更强的清除,这显然有助于它们适应最高的山地。我们的研究结果揭示了植物是如何耐受极端高原的,这将为物种保护和作物育种提供潜在的启示。
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
Molecular biology and evolution
Molecular biology and evolution 生物-进化生物学
CiteScore
19.70
自引率
3.70%
发文量
257
审稿时长
1 months
期刊介绍: Molecular Biology and Evolution Journal Overview: Publishes research at the interface of molecular (including genomics) and evolutionary biology Considers manuscripts containing patterns, processes, and predictions at all levels of organization: population, taxonomic, functional, and phenotypic Interested in fundamental discoveries, new and improved methods, resources, technologies, and theories advancing evolutionary research Publishes balanced reviews of recent developments in genome evolution and forward-looking perspectives suggesting future directions in molecular evolution applications.
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