TY - JOUR
T1 - Expression patterns of two tobacco isoflavone reductase-like genes and their possible roles in secondary metabolism in tobacco
AU - Shoji, Tsubasa
AU - Winz, Robert
AU - Iwase, Tadayuki
AU - Nakajima, Keiji
AU - Yamada, Yasuyuki
AU - Hashimoto, Takashi
N1 - Funding Information:
We would like to thank N.G. Lewis, Washington State University, for DDC, DDDC, TDDC and pSBETa, J.-P. Nap, Center for Plant Breeding and Reproduction, for pLM9, and K. Nakamura, Nagoya University, for ODC cDNA. This research was supported by a grant (JSPS-RFTR00L01605) from the Japan Society for the Promotion of Science to T.H. T.S. was supported by a Japan Society for the Promotion of Science Research Fellowship for Young Scientists (No. 6537).
PY - 2002/10
Y1 - 2002/10
N2 - Plants contain a large number of proteins homologous to isoflavone reductase, an NADPH-dependent reductase involved in the biosynthesis of isoflavonoid phytoalexins in legumes. Although some are bona fide isoflavone reductases, others may catalyze distinct reductase reactions. Two tobacco genes, TP7 and A622, encoding isoflavone reductase-like proteins, had been previously identified from their unique expression patterns, but their functions were not known. We show here that TP7 is a tobacco phenylcoumaran benzylic ether reductase involved in lignan biosynthesis, but that A622 is not. To gain insight into the possible function of A622, we analyzed in detail the expression patterns of the A622 gene by RNA and protein blots, immunohistochemistry, and its promoter expression in transgenic Nicotiana sylvestris roots. The A622 expression patterns were qualitatively similar to those of putrescine N-methyltransferase, the first enzyme in nicotine biosynthesis, suggesting that A622 may function in the metabolism of nicotine or related alkaloids.
AB - Plants contain a large number of proteins homologous to isoflavone reductase, an NADPH-dependent reductase involved in the biosynthesis of isoflavonoid phytoalexins in legumes. Although some are bona fide isoflavone reductases, others may catalyze distinct reductase reactions. Two tobacco genes, TP7 and A622, encoding isoflavone reductase-like proteins, had been previously identified from their unique expression patterns, but their functions were not known. We show here that TP7 is a tobacco phenylcoumaran benzylic ether reductase involved in lignan biosynthesis, but that A622 is not. To gain insight into the possible function of A622, we analyzed in detail the expression patterns of the A622 gene by RNA and protein blots, immunohistochemistry, and its promoter expression in transgenic Nicotiana sylvestris roots. The A622 expression patterns were qualitatively similar to those of putrescine N-methyltransferase, the first enzyme in nicotine biosynthesis, suggesting that A622 may function in the metabolism of nicotine or related alkaloids.
KW - Jasmonate
KW - Lignan
KW - NADPH-dependent oxidoreductase
KW - Nicotiana
KW - Nicotine
KW - Phenylcoumaran benzylic ether reductase
UR - http://www.scopus.com/inward/record.url?scp=0036791456&partnerID=8YFLogxK
U2 - 10.1023/A:1019867732278
DO - 10.1023/A:1019867732278
M3 - 学術論文
C2 - 12369619
AN - SCOPUS:0036791456
SN - 0167-4412
VL - 50
SP - 427
EP - 440
JO - Plant Molecular Biology
JF - Plant Molecular Biology
IS - 3
ER -