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通过突变分析鉴定的 DOC2 蛋白是质膜胞吐所必需的。

A DOC2 protein identified by mutational profiling is essential for apicomplexan parasite exocytosis.

机构信息

Department of Biology, Boston College, Chestnut Hill, MA 02467, USA.

出版信息

Science. 2012 Jan 13;335(6065):218-21. doi: 10.1126/science.1210829.

Abstract

Exocytosis is essential to the lytic cycle of apicomplexan parasites and required for the pathogenesis of toxoplasmosis and malaria. DOC2 proteins recruit the membrane fusion machinery required for exocytosis in a Ca(2+)-dependent fashion. Here, the phenotype of a Toxoplasma gondii conditional mutant impaired in host cell invasion and egress was pinpointed to a defect in secretion of the micronemes, an apicomplexan-specific organelle that contains adhesion proteins. Whole-genome sequencing identified the etiological point mutation in TgDOC2.1. A conditional allele of the orthologous gene engineered into Plasmodium falciparum was also defective in microneme secretion. However, the major effect was on invasion, suggesting that microneme secretion is dispensable for Plasmodium egress.

摘要

胞吐作用对于顶复门寄生虫的裂解周期至关重要,也是弓形体病和疟疾发病机制所必需的。DOC2 蛋白以 Ca2+依赖性方式募集胞吐作用所需的膜融合机制。在这里,宿主细胞入侵和退出缺陷的条件性 Toxoplasma gondii 突变体的表型被精确定位到微线体分泌缺陷,微线体是一种顶复门特有的细胞器,包含粘附蛋白。全基因组测序确定了 TgDOC2.1 中的病因点突变。在疟原虫中构建的同源基因的条件等位基因也在微线体分泌中缺陷。然而,主要影响是入侵,表明微线体分泌对于疟原虫退出是可有可无的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7cf/3354045/14623f02ebd3/nihms360643f1.jpg

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