Thousands of Pristionchus pacificus orphan genes were integrated into developmental networks that respond to diverse environmental microbiota.

IF 4.5 2区 生物学 Q1 Agricultural and Biological Sciences PLoS Genetics Pub Date : 2023-07-01 DOI:10.1371/journal.pgen.1010832
Marina Athanasouli, Nermin Akduman, Waltraud Röseler, Penghieng Theam, Christian Rödelsperger
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Abstract

Adaptation of organisms to environmental change may be facilitated by the creation of new genes. New genes without homologs in other lineages are known as taxonomically-restricted orphan genes and may result from divergence or de novo formation. Previously, we have extensively characterized the evolution and origin of such orphan genes in the nematode model organism Pristionchus pacificus. Here, we employ large-scale transcriptomics to establish potential functional associations and to measure the degree of transcriptional plasticity among orphan genes. Specifically, we analyzed 24 RNA-seq samples from adult P. pacificus worms raised on 24 different monoxenic bacterial cultures. Based on coexpression analysis, we identified 28 large modules that harbor 3,727 diplogastrid-specific orphan genes and that respond dynamically to different bacteria. These coexpression modules have distinct regulatory architecture and also exhibit differential expression patterns across development suggesting a link between bacterial response networks and development. Phylostratigraphy revealed a considerably high number of family- and even species-specific orphan genes in certain coexpression modules. This suggests that new genes are not attached randomly to existing cellular networks and that integration can happen very fast. Integrative analysis of protein domains, gene expression and ortholog data facilitated the assignments of biological labels for 22 coexpression modules with one of the largest, fast-evolving module being associated with spermatogenesis. In summary, this work presents the first functional annotation for thousands of P. pacificus orphan genes and reveals insights into their integration into environmentally responsive gene networks.

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数以千计的太平洋囚徒孤儿基因被整合到响应不同环境微生物群的发育网络中。
新基因的产生可以促进生物体对环境变化的适应。在其他谱系中没有同系物的新基因被称为分类限制性孤儿基因,可能是分化或新生形成的结果。以前,我们已经广泛地描述了这种孤儿基因在线虫模式生物太平洋Pristionchus中的进化和起源。在这里,我们采用大规模转录组学来建立潜在的功能关联,并测量孤儿基因之间的转录可塑性程度。具体来说,我们分析了24份来自24种不同单氧细菌培养的太平洋p.p ificus成虫的RNA-seq样本。基于共表达分析,我们确定了28个大模块,其中包含3,727个双胃特异性孤儿基因,并对不同的细菌动态响应。这些共表达模块具有独特的调控结构,并且在整个发育过程中表现出不同的表达模式,这表明细菌反应网络与发育之间存在联系。系统地层学揭示了在某些共表达模块中有相当多的家族甚至物种特异性孤儿基因。这表明,新的基因并不是随机附着在现有的细胞网络上,这种整合可以非常迅速地发生。蛋白质结构域、基因表达和同源数据的综合分析促进了22个共表达模块的生物标记分配,其中最大的、快速进化的模块与精子发生有关。总之,这项工作提出了第一个功能注释数千太平洋p.p ificus孤儿基因,并揭示了他们整合到环境响应基因网络的见解。
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来源期刊
PLoS Genetics
PLoS Genetics 生物-遗传学
CiteScore
8.10
自引率
2.20%
发文量
438
审稿时长
1 months
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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