| Literature DB >> 27978434 |
Damien Jacot1, Nicolò Tosetti1, Isa Pires2, Jessica Stock3, Arnault Graindorge1, Yu-Fu Hung2, Huijong Han2, Rita Tewari3, Inari Kursula4, Dominique Soldati-Favre5.
Abstract
Apicomplexa exhibit a unique form of substrate-dependent gliding motility central for host cell invasion and parasite dissemination. Gliding is powered by rearward translocation of apically secreted transmembrane adhesins via their interaction with the parasite actomyosin system. We report a conserved armadillo and pleckstrin homology (PH) domain-containing protein, termed glideosome-associated connector (GAC), that mediates apicomplexan gliding motility, invasion, and egress by connecting the micronemal adhesins with the actomyosin system. TgGAC binds to and stabilizes filamentous actin and specifically associates with the transmembrane adhesin TgMIC2. GAC localizes to the apical pole in invasive stages of Toxoplasma gondii and Plasmodium berghei, and apical positioning of TgGAC depends on an apical lysine methyltransferase, TgAKMT. GAC PH domain also binds to phosphatidic acid, a lipid mediator associated with microneme exocytosis. Collectively, these findings indicate a central role for GAC in spatially and temporally coordinating gliding motility and invasion.Entities:
Keywords: actin dynamic; apicomplexa; glideosome; gliding motility; invasion and egress; lysine methyltransferase; microneme; phosphatidic acid; plasmodium; toxoplasma
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Year: 2016 PMID: 27978434 DOI: 10.1016/j.chom.2016.10.020
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023