Population structure and punctuated genomic hyper-diversity in Caenorhabditis briggsae.

IF 6.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nicolas D Moya, Bowen Wang, Robyn E Tanny, Michael E G Sauria, Lance M O'Connor, Ayeh Khorshidian, Ryan McKeown, Charlie Gosse, Clayton M Dilks, Timothy A Crombie, Gaotian Zhang, Emha Rais, Lise Frézal, Viet Dai Dang, Elkana Haryoso, Mia P Devi, Clotilde Gimond, Daniel E Cook, Jung-Chen Hsu, Amanda O Shaver, Stefan Zdraljevic, Aurélien Richaud, Tongshu Wen, Aatira Mehraj, Sharanya H, Karthick Raja Arulprakasam, Emily J Koury, Nicole M Roberto, Etta S Schaye, Varsha Singh, Hagus Tarno, Michael Ailion, Annalise B Paaby, Zhongying Zhao, Asher D Cutter, John Wang, Matthew V Rockman, Marie-Anne Félix, Christian Braendle, Erik C Andersen
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引用次数: 0

Abstract

Comparative genomics provides a powerful framework to uncover the molecular and evolutionary mechanisms that shape genetic diversity, revealing how shared or lineage-specific processes influence their evolutionary trajectories. The nematode Caenorhabditis briggsae is distributed world-wide and is a comparative model to Caenorhabditis elegans in the biology of development, cellular mechanisms, neurobiology, complex trait mappings, and evolution. Following massive collection efforts by the nematode research community, we present the isolation of over 1,900 wild strains and analyses of genome sequences that catalog over six million single-nucleotide and insertion-deletion variants. These resources provide a powerful means to interrogate the causal genetic bases of phenotypic variation. Additionally, we describe C. briggsae population structure and discover new, genetically distinct groups within this primarily self-fertilizing species, including groups of highly related strains sampled across entire continents. We leveraged expansive genetic variation to decipher the effects of linkage and selection on the distribution of genetic diversity across the genome and across geographic regions. Within the species, we find genomic regions with extremely high levels of genetic variation similar to hyper-divergent regions found in C. elegans and other species. These regions harbor new genes and variation enriched for environmental sensing and pathogen responses. Based on comparisons to the outbreeding sister species Caenorhabditis nigoni, we conclude that long-term balancing selection has maintained substantial functional variation, likely associated with ecological variation, within C. briggsae since its divergence from an outbreeding ancestor. Overall, this massive strain resource enables future comparative genetics studies, including genome-wide association study contrasts between Caenorhabditis species.

briggsae杆状线虫种群结构和间断的基因组超多样性。
比较基因组学提供了一个强大的框架来揭示塑造遗传多样性的分子和进化机制,揭示共享或谱系特异性过程如何影响其进化轨迹。秀丽隐杆线虫分布在世界各地,是秀丽隐杆线虫在发育生物学、细胞机制、神经生物学、复杂性状映射和进化方面的比较模型。经过线虫研究界的大量收集工作,我们提出了超过1900种野生菌株的分离和基因组序列的分析,目录超过600万个单核苷酸和插入-删除变体。这些资源为询问表型变异的因果遗传基础提供了有力的手段。此外,我们描述了C. briggsae种群结构,并在这个主要自交受精的物种中发现了新的、遗传上不同的群体,包括在整个大陆取样的高度相关菌株群体。我们利用广泛的遗传变异来破译连锁和选择对遗传多样性在基因组和跨地理区域分布的影响。在该物种中,我们发现具有极高水平遗传变异的基因组区域,类似于秀丽隐杆线虫和其他物种中发现的高度分化区域。这些区域蕴藏着新的基因和变异,丰富了环境感知和病原体反应。通过与远交姐妹种nigoni Caenorhabditis的比较,我们得出结论,自其与远交祖先分化以来,长时间的平衡选择保持了大量的功能变异,可能与生态变异有关。总的来说,这种巨大的菌株资源使未来的比较遗传学研究成为可能,包括线虫物种之间的全基因组关联研究对比。
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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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