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Rapid Gene Family Evolution of a Nematode Sperm Protein Despite Sequence Hyper-conservation

机译:尽管序列超保守线虫精子蛋白的快速基因家族进化。

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摘要

Reproductive proteins are often observed to be the most rapidly evolving elements within eukaryotic genomes. The major sperm protein (MSP) is unique to the phylum Nematoda and is required for proper sperm locomotion and fertilization. Here, we annotate the MSP gene family and analyze their molecular evolution in 10 representative species across Nematoda. We show that MSPs are hyper-conserved across the phylum, having maintained an amino acid sequence identity of 83.5–97.7% for over 500 million years. This extremely slow rate of evolution makes MSPs some of the most highly conserved genes yet identified. However, at the gene family level, we show hyper-variability in both gene copy number and genomic position within species, suggesting rapid, lineage-specific gene family evolution. Additionally, we find evidence that extensive gene conversion contributes to the maintenance of sequence identity within chromosome-level clusters of MSP genes. Thus, while not conforming to the standard expectation for the evolution of reproductive proteins, our analysis of the molecular evolution of the MSP gene family is nonetheless consistent with the widely repeatable observation that reproductive proteins evolve rapidly, in this case in terms of the genomic properties of gene structure, copy number, and genomic organization. This unusual evolutionary pattern is likely generated by strong pleiotropic constraints acting on these genes at the sequence level, balanced against expansion at the level of the whole gene family.
机译:通常观察到生殖蛋白是真核生物基因组中发展最快的元素。主要的精子蛋白(MSP)是线虫门所特有的,是精子活动和受精所必需的。在这里,我们注释了MSP基因家族,并分析了其在整个线虫中的10种代表性物种的分子进化。我们显示,MSP在整个门上都是超保守的,在超过5亿年的时间里一直保持83.5–97.7%的氨基酸序列同一性。这种极慢的进化速度使MSP成为了一些迄今仍被高度保守的基因。但是,在基因家族水平上,我们在物种内的基因拷贝数和基因组位置均显示出高度变异性,表明物种谱系家族快速快速进化。此外,我们发现证据表明广泛的基因转换有助于维持MSP基因的染色体水平簇内的序列同一性。因此,尽管不符合生殖蛋白进化的标准期望,但我们对MSP基因家族的分子进化的分析与生殖蛋白迅速进化的广泛可重复观察一致,在这种情况下,就基因组特性而言的基因结构,拷贝数和基因组组织。这种不寻常的进化模式很可能是由在序列水平上作用于这些基因的强大多效性约束所产生的,与整个基因家族水平上的扩展相平衡。

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