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Cited 47 time in webofscience Cited 46 time in scopus
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Abnormal chloroplast development and growth inhibition in rice thioredoxin m knock-down plantsopen access

Authors
Chi, Yong HunMoon, Jeong ChanPark, Jin HoKim, Ho-SeungZulfugarov, Ismayil S.Fanata, Wahyu IndraJang, Ho HeeLee, Jung RoLee, Young MeeKim, Sun TaeChung, Yong-YoonLim, Chae OhKim, Jae-YeanYun, Dae-JinLee, Choon-HwanLee, Kyun OhLee, Sang Yeol
Issue Date
Oct-2008
Publisher
AMER SOC PLANT BIOLOGISTS
Citation
PLANT PHYSIOLOGY, v.148, no.2, pp.808 - 817
Indexed
SCIE
SCOPUS
Journal Title
PLANT PHYSIOLOGY
Volume
148
Number
2
Start Page
808
End Page
817
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/27251
DOI
10.1104/pp.108.123547
ISSN
0032-0889
Abstract
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 mu mol 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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