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两种截然不同的共生体中进化出了雄性杀手的常见和独特策略。

Common and unique strategies of male killing evolved in two distinct symbionts.

机构信息

Global Health Institute, School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Station 19, CH-1015 Lausanne, Switzerland

Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8566, Japan.

出版信息

Proc Biol Sci. 2018 Mar 28;285(1875). doi: 10.1098/rspb.2017.2167.

Abstract

Male killing is a selfish reproductive manipulation caused by symbiotic bacteria, where male offspring of infected hosts are selectively killed. The underlying mechanisms and the process of their evolution are of great interest not only in terms of fundamental biology, but also their potential applications. The two bacterial symbionts, and , have independently evolved male-killing ability. This raises the question whether the underlying mechanisms share some similarities or are specific to each bacterial species. Here, we analyse pathogenic phenotypes of infected with its natural male-killing strain and compare them with those of infected with male-killing We show that male progeny infected with the strain die during embryogenesis with abnormal apoptosis. Interestingly, male-killing infection induces DNA damage and segregation defects in the dosage-compensated chromosome in male embryos, which are reminiscent of the phenotypes caused by male-killing in By contrast, host neural development seems to proceed normally unlike male-killing infection. Our results demonstrate that the dosage-compensated chromosome is a common target of two distinct male killers, yet uniquely evolved the ability to damage neural tissue of male embryos.

摘要

雄性致死是一种由共生细菌引起的自私生殖操纵,受感染宿主的雄性后代会被选择性杀死。这些机制以及它们进化的过程不仅在基础生物学方面具有重要意义,而且在潜在应用方面也具有重要意义。两种细菌共生体 和 已经独立进化出了雄性致死能力。这就提出了一个问题,即潜在的机制是否存在一些相似之处,还是每种细菌都有其独特的机制。在这里,我们分析了受其自然雄性致死菌株感染的 以及受雄性致死菌株感染的 的致病性表型。我们发现,感染 菌株的雄性后代在胚胎发生过程中因异常凋亡而死亡。有趣的是,雄性致死 感染会导致雄性胚胎中剂量补偿染色体的 DNA 损伤和分离缺陷,这让人联想到雄性致死 在 中引起的表型。相比之下,宿主的神经发育似乎与雄性致死 感染不同,进展正常。我们的结果表明,剂量补偿染色体是两种不同雄性杀手的共同靶标,但 独特地进化出了破坏雄性胚胎神经组织的能力。

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