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Abnormal Chloroplast Development and Growth Inhibition in Rice ThioredoxinmKnock-Down Plants
Author(s) -
Yong Hun,
Jeong Chan Moon,
Jinho Park,
Ho-Seung Kim,
Ismayil S. Zulfugarov,
Wahyu Indra Duwi Fanata,
Ho Hee Jang,
Jung Ro Lee,
YoungMee Lee,
Sun Tae Kim,
Yong-Yoon Chung,
Chae Oh Lim,
JaeYean Kim,
DaeJin Yun,
Choon-Hwan Lee,
Kyun Oh Lee,
Sang Yeol Lee
Publication year - 2008
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.108.123547
Subject(s) - chloroplast , biology , thioredoxin , botany , gene , genetics
Plant cells contain several thioredoxin isoforms that are characterized by subcellular localization and substrate specificity. Here, we describe the functional characterization of a rice (Oryza sativa) thioredoxin m isoform (Ostrxm) using a reverse genetics technique. Ostrxm showed green tissue-specific and light-responsive mRNA expression. Ostrxm was localized in chloroplasts of rice mesophyll cells, and the recombinant protein showed dithiothreitol-dependent insulin beta-chain reduction activity in vitro. RNA interference (RNAi) of Ostrxm resulted in rice plants with developmental defects, including semidwarfism, pale-green leaves, abnormal chloroplast structure, and reduced carotenoid and chlorophyll content. Ostrxm RNAi plants showed remarkably decreased F(v)/F(m) values under high irradiance conditions (1,000 micromol m(-2) s(-1)) with delayed recovery. Two-dimensional electrophoresis and matrix-assisted laser-desorption/ionization time-of-flight analysis showed that the levels of several chloroplast proteins critical for photosynthesis and biogenesis were significantly decreased in Ostrxm RNAi plants. Furthermore, 2-Cys peroxiredoxin, a known target of thioredoxin, was present in oxidized forms, and hydrogen peroxide levels were increased in Ostrxm RNAi plants. The pleiotropic effects of Ostrxm RNAi suggest that Ostrxm plays an important role in the redox regulation of chloroplast target proteins involved in diverse physiological functions.

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