Robert W. Holley Center for Agriculture and Health, USDA-ARS, Cornell University, Ithaca, NY, USA.
Plant Breeding and Genetics Section, School of Integrative Plant Science, Cornell University, Ithaca, NY, USA.
J Exp Bot. 2021 Feb 24;72(4):1059-1072. doi: 10.1093/jxb/eraa528.
Chloroplast-targeted proteins are actively imported into chloroplasts via the machinery spanning the double-layered membranes of chloroplasts. While the key translocons at the outer (TOC) and inner (TIC) membranes of chloroplasts are defined, proteins that interact with the core components to facilitate pre-protein import are continuously being discovered. A DnaJ-like chaperone ORANGE (OR) protein is known to regulate carotenoid biosynthesis as well as plastid biogenesis and development. In this study, we found that OR physically interacts with several Tic proteins including Tic20, Tic40, and Tic110 in the classic TIC core complex of the chloroplast import machinery. Knocking out or and its homolog or-like greatly affects the import efficiency of some photosynthetic and non-photosynthetic pre-proteins. Consistent with the direct interactions of OR with Tic proteins, the binding efficiency assay revealed that the effect of OR occurs at translocation at the inner envelope membrane (i.e. at the TIC complex). OR is able to reduce the Tic40 protein turnover rate through its chaperone activity. Moreover, OR was found to interfere with the interaction between Tic40 and Tic110, and reduces the binding of pre-proteins to Tic110 in aiding their release for translocation and processing. Our findings suggest that OR plays a new and regulatory role in stabilizing key translocons and in facilitating the late stage of plastid pre-protein translocation to regulate plastid pre-protein import.
质体靶向蛋白通过跨越质体双层膜的机制被主动导入质体。虽然已经定义了质体中外膜(TOC)和内膜(TIC)的关键转运体,但不断发现与核心组件相互作用以促进前体蛋白导入的蛋白质。已知 DnaJ 样伴侣蛋白 ORANGE(OR)蛋白可调节类胡萝卜素生物合成以及质体生物发生和发育。在这项研究中,我们发现 OR 与包括 Tic20、Tic40 和 Tic110 在内的几种 Tic 蛋白在质体导入机制的经典 TIC 核心复合物中发生物理相互作用。敲除或及其同源物或样蛋白会极大地影响一些光合和非光合前体蛋白的导入效率。与 OR 与 Tic 蛋白的直接相互作用一致,结合效率测定表明,OR 的作用发生在内膜转运(即在 TIC 复合物处)。OR 能够通过其伴侣活性降低 Tic40 蛋白的周转率。此外,发现 OR 干扰 Tic40 和 Tic110 之间的相互作用,并降低 Tic110 与前体蛋白的结合,以帮助它们释放进行转运和加工。我们的研究结果表明,OR 在稳定关键转运体和促进质体前体蛋白的晚期转运以调节质体前体蛋白导入方面发挥了新的调节作用。