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豌豆与真菌病原体亲和互作过程中12-氧代植物二烯酸10,11-还原酶基因的表达

Expression of the 12-oxophytodienoic acid 10,11-reductase gene in the compatible interaction between pea and fungal pathogen.

作者信息

Ishiga Yasuhiro, Funato Akiko, Tachiki Tomoyuki, Toyoda Kazuhiro, Shiraishi Tomonori, Yamada Tetsuji, Ichinose Yuki

机构信息

Laboratory of Plant Pathology and Genetic Engineering, Faculty of Agriculture, Okayama University, Tsushima-naka, 1-1-1 Okayama, 700-8530 Japan.

出版信息

Plant Cell Physiol. 2002 Oct;43(10):1210-20. doi: 10.1093/pcp/pcf144.

Abstract

Suppressors produced by Mycosphaerella pinodes are glycopeptides to block pea defense responses induced by elicitors. A clone, S64, was isolated as cDNA for suppressor-inducible gene from pea epicotyls. The treatment of pea epicotyls with suppressor alone induced an increase of S64 mRNA within 1 h, and it reached a maximum level at 3 h after treatment. The induction was not affected by application of the elicitor, indicating that the suppressor has a dominant action to regulate S64 gene expression. S64 was also induced by inoculation with a virulent pathogen, M. pinodes, but not by inoculation with a non-pathogen, Ascochyta rabiei, nor by treatment with fungal elicitor. The deduced structure of S64 showed high homology to 12-oxophytodienoic acid reductase (OPR) in Arabidopsis thaliana. A recombinant protein derived from S64 had OPR activity, suggesting compatibility-specific activation of the octadecanoid pathway in plants. Treatment with jasmonic acid (JA) or methyl jasmonic acid, end products of the octadecanoid pathway, inhibited the elicitor-induced accumulation of PAL mRNA in pea. These results indicate that the suppressor-induced S64 gene expression leads to the production of JA or related compounds, which might contribute to the establishment of compatibility by inhibiting the phenylpropanoid biosynthetic pathway.

摘要

由豌豆小球腔菌产生的抑制因子是糖肽,可阻断激发子诱导的豌豆防御反应。从豌豆上胚轴中分离出一个克隆体S64,作为抑制因子诱导基因的cDNA。单独用抑制因子处理豌豆上胚轴会在1小时内诱导S64 mRNA增加,处理后3小时达到最高水平。这种诱导不受激发子应用的影响,表明抑制因子在调节S64基因表达方面具有主导作用。接种强致病性病原体豌豆小球腔菌也可诱导S64,但接种非病原体菜豆壳二孢菌或用真菌激发子处理则不能诱导。推导的S64结构与拟南芥中的12-氧代植物二烯酸还原酶(OPR)具有高度同源性。源自S64的重组蛋白具有OPR活性,表明植物中十八烷酸途径存在相容性特异性激活。用十八烷酸途径的终产物茉莉酸(JA)或茉莉酸甲酯处理可抑制激发子诱导的豌豆中苯丙氨酸解氨酶(PAL)mRNA的积累。这些结果表明,抑制因子诱导的S64基因表达导致JA或相关化合物的产生,这可能通过抑制苯丙烷生物合成途径有助于建立相容性。

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