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Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes: molecular insight into sex-specific processes and translational repression.恶性疟原虫配子体的转录组和蛋白质组综合分析:对性别特异性过程和翻译抑制的分子洞察
Nucleic Acids Res. 2016 Jul 27;44(13):6087-101. doi: 10.1093/nar/gkw536. Epub 2016 Jun 13.
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Changes in lipid composition during sexual development of the malaria parasite Plasmodium falciparum.恶性疟原虫在性发育过程中脂质组成的变化。
Malar J. 2016 Feb 6;15:73. doi: 10.1186/s12936-016-1130-z.
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Global transcriptional repression: An initial and essential step for Plasmodium sexual development.全球转录抑制:疟原虫有性发育的初始且关键步骤。
Proc Natl Acad Sci U S A. 2015 Oct 13;112(41):12824-9. doi: 10.1073/pnas.1504389112. Epub 2015 Sep 28.
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Profiling the Essential Nature of Lipid Metabolism in Asexual Blood and Gametocyte Stages of Plasmodium falciparum.剖析恶性疟原虫无性血液期和配子体期脂质代谢的本质特性。
Cell Host Microbe. 2015 Sep 9;18(3):371-81. doi: 10.1016/j.chom.2015.08.003.
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Genetic investigation of tricarboxylic acid metabolism during the Plasmodium falciparum life cycle.恶性疟原虫生命周期中三羧酸代谢的遗传学研究。
Cell Rep. 2015 Apr 7;11(1):164-74. doi: 10.1016/j.celrep.2015.03.011. Epub 2015 Apr 2.
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Transcriptional profiling defines dynamics of parasite tissue sequestration during malaria infection.转录谱分析定义了疟疾感染过程中寄生虫组织隔离的动态变化。
Genome Med. 2015 Feb 27;7(1):19. doi: 10.1186/s13073-015-0133-7. eCollection 2015.
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The cell biology of malaria infection of mosquito: advances and opportunities.疟原虫感染蚊子的细胞生物学:进展与机遇
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Changes in metabolic phenotypes of Plasmodium falciparum in vitro cultures during gametocyte development.恶性疟原虫配子体发育过程中体外培养代谢表型的变化。
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Translational regulation during stage transitions in malaria parasites.疟原虫阶段转换过程中的翻译调控。
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Organization and function of an actin cytoskeleton in Plasmodium falciparum gametocytes.恶性疟原虫配子体中肌动蛋白细胞骨架的组织与功能
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从成熟雄配子体和雌配子体蛋白质组揭示人类疟原虫的性别特异性生物学特性。

Sex-Specific Biology of the Human Malaria Parasite Revealed from the Proteomes of Mature Male and Female Gametocytes.

作者信息

Miao Jun, Chen Zhao, Wang Zenglei, Shrestha Sony, Li Xiaolian, Li Runze, Cui Liwang

机构信息

From the ‡Department of Entomology, The Pennsylvania State University, 501 ASI Building, University Park, Pennsylvania 16802;

§Department of Statistics, The Pennsylvania State University, 413 Thomas Building, University Park, Pennsylvania 16802.

出版信息

Mol Cell Proteomics. 2017 Apr;16(4):537-551. doi: 10.1074/mcp.M116.061804. Epub 2017 Jan 26.

DOI:10.1074/mcp.M116.061804
PMID:28126901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5383777/
Abstract

The gametocytes of the malaria parasites are obligate for perpetuating the parasite's life cycle through mosquitoes, but the sex-specific biology of gametocytes is poorly understood. We generated a transgenic line in the human malaria parasite , which allowed us to accurately separate male and female gametocytes by flow cytometry. In-depth analysis of the proteomes by liquid chromatography-tandem mass spectrometry identified 1244 and 1387 proteins in mature male and female gametocytes, respectively. GFP-tagging of nine selected proteins confirmed their sex-partitions to be agreeable with the results from the proteomic analysis. The sex-specific proteomes showed significant differences that are consistent with the divergent functions of the two sexes. Although the male-specific proteome (119 proteins) is enriched in proteins associated with the flagella and genome replication, the female-specific proteome (262 proteins) is more abundant in proteins involved in metabolism, translation and organellar functions. Compared with the sex-specific proteomes, this study revealed both extensive conservation and considerable divergence between these two species, which reflect the disparities between the two species in proteins involved in cytoskeleton, lipid metabolism and protein degradation. Comparison with three sex-specific proteomes allowed us to obtain high-confidence lists of 73 and 89 core male- and female-specific/biased proteins conserved in The identification of sex-specific/biased proteomes in lays a solid foundation for understanding the molecular mechanisms underlying the unique sex-specific biology in this early-branching eukaryote.

摘要

疟原虫的配子体对于通过蚊子延续寄生虫的生命周期至关重要,但配子体的性别特异性生物学却知之甚少。我们在人类疟原虫中构建了一个转基因品系,这使我们能够通过流式细胞术准确分离雄性和雌性配子体。通过液相色谱-串联质谱对蛋白质组进行深入分析,分别在成熟雄性和雌性配子体中鉴定出1244种和1387种蛋白质。对九种选定蛋白质进行绿色荧光蛋白标记,证实它们的性别划分与蛋白质组分析结果一致。性别特异性蛋白质组显示出显著差异,这与两性的不同功能一致。虽然雄性特异性蛋白质组(119种蛋白质)富含与鞭毛和基因组复制相关的蛋白质,但雌性特异性蛋白质组(262种蛋白质)在参与代谢、翻译和细胞器功能的蛋白质中更为丰富。与性别特异性蛋白质组相比,本研究揭示了这两个物种之间既有广泛的保守性,也有相当大的差异,这反映了这两个物种在参与细胞骨架、脂质代谢和蛋白质降解的蛋白质方面的差异。与三个性别特异性蛋白质组进行比较,使我们获得了在[具体物种]中保守的73种和89种核心雄性和雌性特异性/偏向性蛋白质的高可信度列表。在[具体物种]中鉴定性别特异性/偏向性蛋白质组为理解这种早期分支真核生物独特的性别特异性生物学的分子机制奠定了坚实基础。