Department for Integrative Evolutionary Biology, Max Planck Institute for Biology Tübingen, Max Planck Ring 9, 72076 Tübingen, Germany.
Genome Biol Evol. 2022 Dec 7;14(12). doi: 10.1093/gbe/evac169.
Whole genome duplication (WGD) is often considered a major driver of evolution that leads to phenotypic novelties. However, the importance of WGD for evolution is still controversial because most documented WGD events occurred anciently and few experimental systems amenable to genetic analysis are available. Here, we report a recent WGD event in the hermaphroditic nematode Allodiplogaster sudhausi and present a comparison with a gonochoristic (male/female) sister species that did not undergo WGD. Self-fertilizing reproduction of A. sudhausi makes it amenable to functional analysis and an ideal system to study WGD events. We document WGD in A. sudhausi through karyotype analysis and whole genome sequencing, the latter of which allowed us to 1) identify functional bias in retention of protein domains and metabolic pathways, 2) show most duplicate genes are under evolutionary constraint, 3) show a link between sequence and expression divergence, and 4) characterize differentially expressed duplicates. We additionally show WGD is associated with increased body size and an abundance of repeat elements (36% of the genome), including a recent expansion of the DNA-hAT/Ac transposon family. Finally, we demonstrate the use of CRISPR/Cas9 to generate mutant knockouts, whereby two WGD-derived duplicate genes display functional redundancy in that they both need to be knocked out to generate a phenotype. Together, we present a novel experimental system that is convenient for examining and characterizing WGD-derived genes both computationally and functionally.
全基因组复制(WGD)通常被认为是导致表型新颖性的进化的主要驱动力。然而,WGD 对进化的重要性仍然存在争议,因为大多数有记录的 WGD 事件发生在很久以前,并且可用的适合遗传分析的实验系统很少。在这里,我们报告了雌雄同体线虫 Allodiplogaster sudhausi 中的一个近期 WGD 事件,并与未经历 WGD 的雌雄异体(雄性/雌性)姐妹种进行了比较。A. sudhausi 的自交繁殖使其适合功能分析,是研究 WGD 事件的理想系统。我们通过染色体组分析和全基因组测序来证明 A. sudhausi 中的 WGD,后者使我们能够 1)确定保留蛋白结构域和代谢途径的功能偏倚,2)表明大多数重复基因受到进化约束,3)显示序列和表达分化之间的联系,以及 4)描述差异表达的重复基因。我们还表明,WGD 与体型增大和重复元件(基因组的 36%)丰度增加有关,包括 DNA-hAT/Ac 转座子家族的近期扩张。最后,我们展示了使用 CRISPR/Cas9 产生突变敲除,其中两个 WGD 衍生的重复基因表现出功能冗余,因为它们都需要敲除才能产生表型。总之,我们提出了一种新的实验系统,方便对 WGD 衍生基因进行计算和功能分析。