TY - JOUR
T1 - Characterization of a rice nuclear-encoded plastid RNA polymerase gene OsRpoTp
AU - Kusumi, Kensuke
AU - Yara, Asanori
AU - Mitsui, Naoko
AU - Tozawa, Yuzuru
AU - Iba, Koh
N1 - Funding Information:
We thank Dr. Y. Niwa (University of Shizuoka) for kindly supplying DNA materials, Dr. H. Satoh (Kyushu University) and Dr. A. Yoshimura (Kyushu University) for supplying the rice seed, Dr. S. Kit-ada (Kyushu University) for the antibody against MPPα, and J. Kusumi (Kyushu University) for the phylogenetic analysis. This work was supported by grants from the Ministry of Agriculture, Forestry and Fisheries of Japan (Rice Genome Projects MP-1112 and IP-5005).
PY - 2004/9
Y1 - 2004/9
N2 - We isolated and characterized two rice genes, OsRpoTp and OsRpoTm, that encode putative phage-type RNA polymerases. Predicted amino acid sequences showed high homology of these genes to known RpoT genes. A transient expression assay using green fluorescent protein indicated that the encoded proteins were localized to plastids and mitochondria, respectively. We demonstrated by reverse transcription-PCR experiments and immunoblot analysis that OsRpoTp expression occurred at an early stage of leaf development, prior to the transcript accumulation of the genes that were transcribed by the nuclear-encoded plastid RNA polymerase (NEP). Expression analyses of the chloroplast-deficient rice mutant, virescent-1, showed a discrepancy between OsRpoTp protein accumulation and the level of transcripts of NEP-transcribed genes. Our results suggest that NEP activation is regulated by a process after transcription, and is affected by the developmental state of chloroplast biogenesis.
AB - We isolated and characterized two rice genes, OsRpoTp and OsRpoTm, that encode putative phage-type RNA polymerases. Predicted amino acid sequences showed high homology of these genes to known RpoT genes. A transient expression assay using green fluorescent protein indicated that the encoded proteins were localized to plastids and mitochondria, respectively. We demonstrated by reverse transcription-PCR experiments and immunoblot analysis that OsRpoTp expression occurred at an early stage of leaf development, prior to the transcript accumulation of the genes that were transcribed by the nuclear-encoded plastid RNA polymerase (NEP). Expression analyses of the chloroplast-deficient rice mutant, virescent-1, showed a discrepancy between OsRpoTp protein accumulation and the level of transcripts of NEP-transcribed genes. Our results suggest that NEP activation is regulated by a process after transcription, and is affected by the developmental state of chloroplast biogenesis.
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U2 - 10.1093/pcp/pch133
DO - 10.1093/pcp/pch133
M3 - Article
C2 - 15509842
AN - SCOPUS:7944231496
SN - 0032-0781
VL - 45
SP - 1194
EP - 1201
JO - Plant and Cell Physiology
JF - Plant and Cell Physiology
IS - 9
ER -