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本文引用的文献

1
Conserved Patterns of Sex Chromosome Dosage Compensation in the Lepidoptera (WZ/ZZ): Insights from a Moth Neo-Z Chromosome.鳞翅目(WZ/ZZ)性染色体剂量补偿的保守模式:来自一种蛾类新Z染色体的见解
Genome Biol Evol. 2017 Mar 1;9(3):802-816. doi: 10.1093/gbe/evx039.
2
Male-killing symbiont damages host's dosage-compensated sex chromosome to induce embryonic apoptosis.雄性致死共生菌破坏宿主的剂量补偿性性染色体,诱导胚胎凋亡。
Nat Commun. 2016 Sep 21;7:12781. doi: 10.1038/ncomms12781.
3
Wolbachia Protein TomO Targets nanos mRNA and Restores Germ Stem Cells in Drosophila Sex-lethal Mutants.沃尔巴克氏体蛋白TomO靶向果蝇nanos信使核糖核酸并恢复性致死突变体中的生殖干细胞。
Curr Biol. 2016 Sep 12;26(17):2223-32. doi: 10.1016/j.cub.2016.06.054. Epub 2016 Aug 4.
4
Male-Killing Spiroplasma Alters Behavior of the Dosage Compensation Complex during Drosophila melanogaster Embryogenesis.杀雄螺原体改变黑腹果蝇胚胎发育过程中剂量补偿复合体的行为。
Curr Biol. 2016 May 23;26(10):1339-45. doi: 10.1016/j.cub.2016.03.050. Epub 2016 May 5.
5
Riboflavin Provisioning Underlies Wolbachia's Fitness Contribution to Its Insect Host.核黄素供应是沃尔巴克氏体对其昆虫宿主适应性做出贡献的基础。
mBio. 2015 Nov 10;6(6):e01732-15. doi: 10.1128/mBio.01732-15.
6
Misdirection of dosage compensation underlies bidirectional sex-specific death in Wolbachia-infected Ostrinia scapulalis.剂量补偿的错误导向是感染沃尔巴克氏体的二化螟双向性别特异性死亡的基础。
Insect Biochem Mol Biol. 2015 Nov;66:72-6. doi: 10.1016/j.ibmb.2015.10.001. Epub 2015 Oct 8.
7
The Endosymbiotic Bacterium Wolbachia Selectively Kills Male Hosts by Targeting the Masculinizing Gene.内共生细菌沃尔巴克氏体通过靶向雄性化基因选择性杀死雄性宿主。
PLoS Pathog. 2015 Jul 14;11(7):e1005048. doi: 10.1371/journal.ppat.1005048. eCollection 2015 Jul.
8
Dosage compensation in Drosophila.果蝇中的剂量补偿效应。
Cold Spring Harb Perspect Biol. 2015 May 1;7(5):a019398. doi: 10.1101/cshperspect.a019398.
9
Reproductive parasitism: maternally inherited symbionts in a biparental world.生殖寄生:双亲世界中的母系遗传共生体。
Cold Spring Harb Perspect Biol. 2015 May 1;7(5):a017699. doi: 10.1101/cshperspect.a017699.
10
Genome sequence of the Drosophila melanogaster male-killing Spiroplasma strain MSRO endosymbiont.果蝇雄性致死螺原体菌株MSRO内共生菌的基因组序列
mBio. 2015 Mar 31;6(2):e02437-14. doi: 10.1128/mBio.02437-14.

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.

DOI:10.1098/rspb.2017.2167
PMID:29563258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5897628/
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。