无性线虫基因组杂合性的得失。

IF 1.8 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Molecular Evolution Pub Date : 2025-08-01 Epub Date: 2025-08-06 DOI:10.1007/s00239-025-10259-3
Ali Amini, John R Bracht
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引用次数: 0

摘要

无性生殖往往导致遗传多样性的丧失,但一些机制已经进化到维持杂合性。地下线虫,Halicephalobus mephisto,孤雌生殖,在这里,我们研究了它的遗传多样性- 1.15%的SNP杂合性-是如何代代相传的。为了检测杂合性的缺失,我们在两个不同的位点对56只动物进行了pcr分型;种群中未见纯合子。此外,对亲本和后代的全基因组分析表明,在超过62万个snp中,没有从杂合子到纯合子的转变。令人惊讶的是,这些snp并不是均匀分布在整个基因组中,因为我们发现在没有变异的地方存在多束杂合性缺失(LOH)。覆盖430万个碱基对(Mb)全基因组,这些LOH束与最近的减数分裂重组事件或染色体分离错误最一致。为了支持这一点,我们观察到生殖过程中的染色体关联可能反映了某种程度的突触,潜在地实现了重组。然而,对双亲-后代对的全基因组分析显示,基因组的当前状态保持稳定,没有检测到新的LOH,这表明H. mephisto的历史比以前认为的更动态,杂合性并不总是保持完美的保真度。这一观察结果的潜在功能和进化后果,以及促进这一不寻常的基因组历史的潜在机制进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gain and Loss of Heterozygosity in the Genome of the Asexual Nematode Halicephalobus mephisto.

Asexual reproduction often leads to loss of genetic diversity, but several mechanisms have evolved to maintain heterozygosity. The subterrestrial nematode, Halicephalobus mephisto, reproduces parthenogenetically, and here, we investigate how its genetic diversity - 1.15% SNP heterozygosity-is retained from generation to generation. To test for loss of heterozygosity, we PCR-typed 56 individual animals at two different loci; no homozygotes were observed in the population. Furthermore, whole-genome analysis of parent and progeny demonstrated no transition from heterozygote to homozygote across over 620,000 SNPs. Surprisingly, these SNPs are not uniformly distributed throughout the genome, as we find multiple tracts of loss of heterozygosity (LOH) where no variation exists. Covering 4.3 million base pairs (Mb) genome-wide, these LOH tracts are most consistent with a recent meiotic recombination event or an error of chromosomal segregation. Supporting this, we observed chromosomal associations during reproduction that may reflect some degree of synapsis, potentially enabling recombination. However, full-genome analysis of parent-progeny pairs shows the current state of the genome remains stable, with no new LOH detectable, suggesting that history of H. mephisto is more dynamic than previously appreciated, and that heterozygosity has not always been retained with perfect fidelity. The potential functional and evolutionary consequences of this observation are discussed along with potential mechanisms contributing to this unusual genomic history.

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来源期刊
Journal of Molecular Evolution
Journal of Molecular Evolution 生物-进化生物学
CiteScore
5.50
自引率
2.60%
发文量
36
审稿时长
3 months
期刊介绍: Journal of Molecular Evolution covers experimental, computational, and theoretical work aimed at deciphering features of molecular evolution and the processes bearing on these features, from the initial formation of macromolecular systems through their evolution at the molecular level, the co-evolution of their functions in cellular and organismal systems, and their influence on organismal adaptation, speciation, and ecology. Topics addressed include the evolution of informational macromolecules and their relation to more complex levels of biological organization, including populations and taxa, as well as the molecular basis for the evolution of ecological interactions of species and the use of molecular data to infer fundamental processes in evolutionary ecology. This coverage accommodates such subfields as new genome sequences, comparative structural and functional genomics, population genetics, the molecular evolution of development, the evolution of gene regulation and gene interaction networks, and in vitro evolution of DNA and RNA, molecular evolutionary ecology, and the development of methods and theory that enable molecular evolutionary inference, including but not limited to, phylogenetic methods.
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