Miao Jun, Chen Zhao, Wang Zenglei, Shrestha Sony, Li Xiaolian, Li Runze, Cui Liwang
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.
Mol Cell Proteomics. 2017 Apr;16(4):537-551. doi: 10.1074/mcp.M116.061804. Epub 2017 Jan 26.
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.
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。