TY - JOUR
T1 - Alternative transcription initiation of the nitrilase gene (BrNIT2) caused by infection with Plasmodiophora brassicae Woron. in Chinese cabbage (Brassica rapa L.)
AU - Ando, Sugihiro
AU - Tsushima, Seiya
AU - Kamachi, Shinichiro
AU - Konagaya, Ken Ichi
AU - Tabei, Yutaka
N1 - Funding Information:
Acknowledgements We thank Dr. T. Suzuki (former researcher at the National Institute of Vegetable and Tea Sciences) for providing the double-haploid B. rapa (cv. Muso), Dr. K. Kageyama (Gifu University) for providing P. brassicae single-spore isolate Ibaraki-1, and Dr. S. Takashita (Nippon Norin Seed Co.) for providing P. brassicae race Kitami. The seeds of B. carinata and B. nigra were kindly gifted by Dr. Y. Matsuzawa and Dr. Y. Kaneko (University of Utsunomiya). The binary vector pSMAH628 was kindly provided by Dr. H. Ichikawa (National Institute of Agrobiological Sciences). This study was supported in part by a Research Fellowship from the Japan Society for the Promotion of Science by Young Scientists (to S. Ando).
Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2008/12
Y1 - 2008/12
N2 - In clubroot disease, gall formation is induced by infection with the obligate biotroph Plasmodiophora brassicae, and cell hypertrophy is dependent on increased auxin levels. The enzyme nitrilase is suggested to play an important role in auxin biosynthesis in plants. Here, we investigated the expression of nitrilase genes in clubroot disease in Chinese cabbage (Brassica rapa L.). We isolated four isogenes of nitrilase (BrNIT1, BrNIT2, BrNIT3, and BrNIT4) from Chinese cabbage. When a BrNIT2-specific probe was used for Northern blot hybridization, enhanced accumulation of a 1.4 kb mRNA and additional shorter transcripts (1.1 kb) were only detected in clubbed roots 25 days postinoculation (dpi) onward. The expression of BrNIT1 was not strongly affected by infection with P. brassicae. BrNIT3 expression was detected in the roots at 10 and 20 dpi, and the expression was less in clubbed roots than in healthy roots at 20 dpi. Analysis of the transcription initiation point of the BrNIT2 gene suggests that 1.1 kb transcripts were generated by alternative transcription initiation between the second intron and the third exon. The sequence from the second intron to half of the third exon (+415 to +1037, 623 bp) had promoter activity in Arabidopsis during clubroot formation. Therefore, our results suggest that transcriptional regulation of BrNIT2 might be involved in auxin overproduction during clubroot development.
AB - In clubroot disease, gall formation is induced by infection with the obligate biotroph Plasmodiophora brassicae, and cell hypertrophy is dependent on increased auxin levels. The enzyme nitrilase is suggested to play an important role in auxin biosynthesis in plants. Here, we investigated the expression of nitrilase genes in clubroot disease in Chinese cabbage (Brassica rapa L.). We isolated four isogenes of nitrilase (BrNIT1, BrNIT2, BrNIT3, and BrNIT4) from Chinese cabbage. When a BrNIT2-specific probe was used for Northern blot hybridization, enhanced accumulation of a 1.4 kb mRNA and additional shorter transcripts (1.1 kb) were only detected in clubbed roots 25 days postinoculation (dpi) onward. The expression of BrNIT1 was not strongly affected by infection with P. brassicae. BrNIT3 expression was detected in the roots at 10 and 20 dpi, and the expression was less in clubbed roots than in healthy roots at 20 dpi. Analysis of the transcription initiation point of the BrNIT2 gene suggests that 1.1 kb transcripts were generated by alternative transcription initiation between the second intron and the third exon. The sequence from the second intron to half of the third exon (+415 to +1037, 623 bp) had promoter activity in Arabidopsis during clubroot formation. Therefore, our results suggest that transcriptional regulation of BrNIT2 might be involved in auxin overproduction during clubroot development.
KW - Auxin
KW - Chinese cabbage
KW - Clubroot
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U2 - 10.1007/s11103-008-9390-9
DO - 10.1007/s11103-008-9390-9
M3 - Article
C2 - 18726557
AN - SCOPUS:54849436834
SN - 0167-4412
VL - 68
SP - 557
EP - 569
JO - Plant Molecular Biology
JF - Plant Molecular Biology
IS - 6
ER -