Smith Matthew D, Hiltbrunner Andreas, Kessler Felix, Schnell Danny J
Department of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA 01003, USA.
J Cell Biol. 2002 Dec 9;159(5):833-43. doi: 10.1083/jcb.200208017.
The multimeric translocon at the outer envelope membrane of chloroplasts (Toc) initiates the recognition and import of nuclear-encoded preproteins into chloroplasts. Two Toc GTPases, Toc159 and Toc33/34, mediate preprotein recognition and regulate preprotein translocation. Although these two proteins account for the requirement of GTP hydrolysis for import, the functional significance of GTP binding and hydrolysis by either GTPase has not been defined. A recent study indicates that Toc159 is equally distributed between a soluble cytoplasmic form and a membrane-inserted form, raising the possibility that it might cycle between the cytoplasm and chloroplast as a soluble preprotein receptor. In the present study, we examined the mechanism of targeting and insertion of the Arabidopsis thaliana orthologue of Toc159, atToc159, to chloroplasts. Targeting of atToc159 to the outer envelope membrane is strictly dependent only on guanine nucleotides. Although GTP is not required for initial binding, the productive insertion and assembly of atToc159 into the Toc complex requires its intrinsic GTPase activity. Targeting is mediated by direct binding between the GTPase domain of atToc159 and the homologous GTPase domain of atToc33, the Arabidopsis Toc33/34 orthologue. Our findings demonstrate a role for the coordinate action of the Toc GTPases in assembly of the functional Toc complex at the chloroplast outer envelope membrane.
叶绿体外被膜上的多聚体转运体(Toc)启动了核编码前体蛋白向叶绿体的识别与导入过程。两种Toc GTP酶,即Toc159和Toc33/34,介导前体蛋白的识别并调节前体蛋白的转运。尽管这两种蛋白说明了导入过程中对GTP水解的需求,但任一GTP酶的GTP结合及水解的功能意义尚未明确。最近一项研究表明,Toc159在可溶性细胞质形式和膜插入形式之间均匀分布,这增加了它可能作为可溶性前体蛋白受体在细胞质和叶绿体之间循环的可能性。在本研究中,我们研究了拟南芥Toc159的同源物atToc159靶向并插入叶绿体的机制。atToc159靶向叶绿体外被膜严格仅依赖于鸟嘌呤核苷酸。虽然初始结合不需要GTP,但atToc159有效插入并组装到Toc复合体中需要其内在的GTP酶活性。靶向作用是由atToc159的GTP酶结构域与拟南芥Toc33/34的同源物atToc33的同源GTP酶结构域之间的直接结合介导的。我们的研究结果证明了Toc GTP酶在叶绿体外被膜上功能性Toc复合体组装中的协同作用。