Thompson Joanne, Fernandez-Reyes Delmiro, Sharling Lisa, Moore Sally G, Eling Wijnand M, Kyes Sue A, Newbold Christopher I, Kafatos Fotis C, Janse Chris J, Waters Andrew P
Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3JT, UK.
Cell Microbiol. 2007 Jun;9(6):1466-80. doi: 10.1111/j.1462-5822.2006.00885.x. Epub 2007 Jan 23.
The Cysteine Repeat Modular Proteins (PCRMP1-4) of Plasmodium, are encoded by a small gene family that is conserved in malaria and other Apicomplexan parasites. They are very large, predicted surface proteins with multipass transmembrane domains containing motifs that are conserved within families of cysteine-rich, predicted surface proteins in a range of unicellular eukaryotes, and a unique combination of protein-binding motifs, including a >100 kDa cysteine-rich modular region, an epidermal growth factor-like domain and a Kringle domain. PCRMP1 and 2 are expressed in life cycle stages in both the mosquito and vertebrate. They colocalize with PfEMP1 (P. falciparum Erythrocyte Membrane Antigen-1) during its export from P. falciparum blood-stage parasites and are exposed on the surface of haemolymph- and salivary gland-sporozoites in the mosquito, consistent with a role in host tissue targeting and invasion. Gene disruption of pcrmp1 and 2 in the rodent malaria model, P. berghei, demonstrated that both are essential for transmission of the parasite from the mosquito to the mouse and has established their discrete and important roles in sporozoite targeting to the mosquito salivary gland. The unprecedented expression pattern and structural features of the PCRMPs thus suggest a variety of roles mediating host-parasite interactions throughout the parasite life cycle.
疟原虫的半胱氨酸重复模块化蛋白(PCRMP1 - 4)由一个小基因家族编码,该家族在疟疾及其他顶复门寄生虫中保守。它们是非常大的预测表面蛋白,具有多次跨膜结构域,包含在一系列单细胞真核生物中富含半胱氨酸的预测表面蛋白家族内保守的基序,以及独特的蛋白结合基序组合,包括一个大于100 kDa的富含半胱氨酸的模块化区域、一个表皮生长因子样结构域和一个kringle结构域。PCRMP1和2在蚊子和脊椎动物的生命周期阶段均有表达。在恶性疟原虫血期寄生虫输出PfEMP1(恶性疟原虫红细胞膜抗原-1)的过程中,它们与PfEMP1共定位,并且在蚊子的血淋巴和唾液腺子孢子表面暴露,这与它们在宿主组织靶向和入侵中的作用一致。在啮齿动物疟疾模型伯氏疟原虫中对pcrmp1和2进行基因破坏表明,二者对于寄生虫从蚊子传播到小鼠都是必不可少的,并确定了它们在子孢子靶向蚊子唾液腺中的独特且重要的作用。因此,PCRMPs前所未有的表达模式和结构特征表明,它们在整个寄生虫生命周期中介导宿主 - 寄生虫相互作用中发挥着多种作用。