Nested likelihood-ratio testing of the nonsynonymous:synonymous ratio suggests greater adaptation in the piRNA machinery of Drosophila melanogaster compared with Drosophila ananassae and Drosophila willistoni, two species with higher repeat content.

IF 2.2 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2025-04-17 DOI:10.1093/g3journal/jkaf017
Justin P Blumenstiel, Sarah B Kingan, Daniel Garrigan, Tom Hill, Jeffrey Vedanayagam
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Abstract

Numerous studies have revealed a signature of strong adaptive evolution in the piwi-interacting RNA (piRNA) machinery of Drosophila melanogaster, but the cause of this pattern is not understood. Several hypotheses have been proposed. One hypothesis is that transposable element (TE) families and the piRNA machinery are co-evolving under an evolutionary arms race, perhaps due to antagonism by TEs against the piRNA machinery. A related, though not co-evolutionary, hypothesis is that recurrent TE invasion drives the piRNA machinery to adapt to novel TE strategies. A third hypothesis is that ongoing fluctuation in TE abundance leads to adaptation in the piRNA machinery that must constantly adjust between sensitivity for detecting new elements and specificity to avoid the cost of off-target gene silencing. Rapid evolution of the piRNA machinery may also be driven independently of TEs, and instead from other functions such as the role of piRNAs in suppressing sex-chromosome meiotic drive. We sought to evaluate the impact of TE abundance on adaptive evolution of the piRNA machinery in D. melanogaster and 2 species with higher repeat content-Drosophila ananassae and Drosophila willistoni. This comparison was achieved by employing a likelihood-based hypothesis testing framework based on the McDonald-Kreitman test. We show that we can reject a faster rate of adaptive evolution in the piRNA machinery of these 2 species. We propose that the high rate of adaptation in D. melanogaster is either driven by a recent influx of TEs that have occurred during range expansion or selection on other functions of the piRNA machinery.

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非同义:同义比值的巢式似然比检验表明,与重复含量较高的果蝇ananassae和Drosophila willistoni相比,黑腹果蝇对piRNA机制的适应性更强。
大量研究揭示了黑腹果蝇piwi相互作用RNA (piRNA)机制的强适应性进化特征,但这种模式的原因尚不清楚。人们提出了几个假设。一种假说认为,转座因子(TE)家族和piRNA机制在进化军备竞赛中共同进化,可能是由于TE对piRNA机制的拮抗作用。一个相关的,尽管不是共同进化的假设是,复发性TE入侵驱使piRNA机制适应新的TE策略。第三种假设是,TE丰度的持续波动导致piRNA机制的适应,必须不断调整检测新元素的敏感性和特异性,以避免脱靶基因沉默的代价。piRNA机制的快速进化也可能独立于TEs,而不是其他功能,如piRNA在抑制性染色体减数分裂驱动中的作用。我们试图评估TE丰度对黑腹果蝇和2种重复序列含量较高的果蝇(Drosophila ananassae)和果蝇(Drosophila willistoni) piRNA机制适应性进化的影响。这种比较是通过采用基于McDonald-Kreitman检验的基于似然的假设检验框架实现的。我们表明,我们可以在这两个物种的piRNA机制中拒绝更快的适应性进化速率。我们认为,黑腹巨鳄的高适应率可能是由最近在范围扩张过程中发生的te涌入或对piRNA机制其他功能的选择所驱动的。
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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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