裸眼蝇x连锁减数分裂驱动的单细胞结果。

IF 3.7 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2025-09-18 eCollection Date: 2025-09-01 DOI:10.1371/journal.pgen.1011816
Peter D Price, Sylvie M Parkus, Victoria J Lloyd, Ben T Alston, Sasha L Bradshaw, Sadé Bates, Margaret A Hughes, Steve Paterson, Terry Burke, Iulia Darolti, Andrew Pomiankowski, Alison E Wright
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引用次数: 0

摘要

性别连锁减数分裂驱动因素限制了异配子性别中交替性染色体的遗传,从而扭曲了后代的性别比例。因此,它们对基因组进化、适应以及性选择特征的出现和维持产生了重大影响。尽管如此,我们对它们的分子基础及其对配子体发生和性染色体调节的影响的理解更广泛地集中在少数模式生物上,主要是果蝇和小鼠,这些生物并不能代表自然界中广泛的生殖模式和驱动系统的多样性。在这里,我们采用单细胞RNA测序(scRNA-seq)来研究马来西亚长柄眼蝇(Teleopsis dalmanni)的性别连锁减数分裂驱动因子。首先,我们制作了一个完整的雄性雄性雄性雄性生殖腺单细胞图谱,并确定了主要的睾丸细胞类型。然后,我们提供了睾丸细胞和转录景观的综合概况,为缺乏完全减数分裂性染色体失活和剂量补偿的复杂轨迹提供了证据。其次,通过对比驱动和标准睾丸之间的单细胞表达数据,我们深入了解了减数分裂驱动对睾丸转录组景观和性染色体调节的影响。重要的是,我们表明减数分裂驱动因子的存在不会扰乱x连锁调控的基本模式。我们的研究结果揭示了减数分裂驱动因子如何将其传递给下一代,并强调了表达紊乱的基因是精子发生破坏的潜在后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-cell consequences of X-linked meiotic drive in stalk-eyed flies.

Sex-linked meiotic drivers limit the inheritance of the alternate sex chromosome in the heterogametic sex, subsequently skewing the offspring sex ratio. They consequently have large impacts on genome evolution, adaptation, and the emergence and maintenance of sexually selected traits. Despite this, our understanding of their molecular basis and consequences for gametogenesis and sex chromosome regulation more broadly has focused on a handful of model organisms, primarily Drosophila and mouse, which are not representative of the broad diversity of reproductive modes and drive systems in nature. Here, we employ single-cell RNA sequencing (scRNA-seq) to investigate a sex-linked meiotic driver in the Malaysian stalk-eyed fly, Teleopsis dalmanni. First, we produce a comprehensive single-cell atlas of the male T. dalmanni gonad and identify major testis cell types. We then provide a comprehensive profile of the cellular and transcriptional landscape of the testis, providing evidence for a lack of complete meiotic sex chromosome inactivation and complex trajectory of dosage compensation. Second, by contrasting single-cell expression data between drive and standard testes, we provide insight into the consequences of a meiotic driver for the transcriptomic landscape of the testis and sex chromosome regulation. Importantly, we show that the presence of a meiotic driver does not perturb fundamental patterns of X-linked regulation. Our results provide insight into how the meiotic driver might bias its transmission to the next generation and highlight genes with perturbed expression as a potential consequence of the disruption of spermatogenesis.

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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
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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