4.7 Article

Arabidopsis ORANGE protein regulates plastid pre-protein import through interacting with Tic proteins

期刊

JOURNAL OF EXPERIMENTAL BOTANY
卷 72, 期 4, 页码 1059-1072

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jxb/eraa528

关键词

Import efficiency; OR; plastid import machinery; protein-protein interaction; Tic40; Tic110

资金

  1. Agriculture and Food Research Initiative competitive award from the U.S. Department of Agriculture (USDA) National Institute of Food and Agriculture [2016-67013-24612]
  2. USDA-Agricultural Research Service fund

向作者/读者索取更多资源

The study reveals that the DnaJ-like chaperone protein ORANGE (OR) interacts with core components of the TIC complex in chloroplasts, impacting the turnover rate of Tic40 protein and interfering with its interaction with Tic110. This interaction aids in the translocation and processing of pre-proteins, indicating a regulatory role for OR in plastid pre-protein import.
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.

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