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首页> 外文期刊>Physiological and Molecular Plant Pathology >Expression of specific (13)-beta-glucanase genes in leaves of near-isogenic resistant and susceptible barley lines infected with the leaf scald fungus (Rhynchosporium secalis).
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Expression of specific (13)-beta-glucanase genes in leaves of near-isogenic resistant and susceptible barley lines infected with the leaf scald fungus (Rhynchosporium secalis).

机译:特定(1 <右箭头> 3)-β-葡聚糖酶基因在被叶鳞真菌(Rhynchosporium secalis)感染的近等基因抗性和易感大麦系的叶片中的表达。

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摘要

Near-isogenic resistant and susceptible lines of barley were inoculated with a virulent race of the leaf scald pathogen R. secalis. The expression patterns of specific barley (13)-beta-glucan endohydrolase (EC 3.2.1.39) isoenzymes weremonitored. Induction of (13)-beta-glucanase activity occurred 1 day earlier and to higher levels in the resistant backcross BC-200 than in the susceptible parent line. The resistant plants of the backcross line responded more rapidly to pathogen invasion than susceptible lines. The increased (13)-beta-glucanase activity was predominantly attributable to a 2-3 day period in which mRNA transcripts of genes that encode isoenzymes GII and GI accumulated. It is suggested that thesegenes may be important in the defence responses of barley backcross line BC-200 to pathogen attack. A second scald-resistant backcross line, BC-30, developed levels of (13)-beta-glucanase similar to BC-200 upon infection, but max. levels were reached later than in BC-200. The third resistant backcross line, BC-35, showed the same pattern of expression as the susceptible parent cultivar, Clipper. The differences in expression of (13)-beta-glucanase between the resistant backcross lines show that there are physiologically distinct modes of resistance to the scald fungus in barley and that one of these at least is accompanied by (13)-beta-glucanase induction.
机译:将近等基因抗性和易感大麦品系接种到叶鳞病原菌R. secalis的强毒小种上。监测特定大麦(1右箭头3)-β-葡聚糖内切酶(EC 3.2.1.39)同工酶的表达模式。 (1右箭头3)-β-葡聚糖酶活性的诱导提前1天发生,并且在抗性回交BC-200中比易感亲本中的水平更高。回交系的抗性植物比易感系对病原体入侵的反应更快。增加的(1 <右箭头> 3)-β-葡聚糖酶活性主要归因于2-3天的时间段,其中编码同工酶GII和GI的基因的mRNA转录物积累。提示这些基因在大麦回交系BC-200对病原体侵袭的防御反应中可能是重要的。第二个耐烫伤性回交系BC-30在感染后发展出与BC-200相似的(1 <右箭头> 3)-β-葡聚糖酶水平,但最高。到达水平比在BC-200以后。第三个抗性回交系BC-35显示了与易感亲本快剪相同的表达模式。抗性回交线之间的(1 <右箭头> 3)-β-葡聚糖酶表达差异表明,大麦对烫伤性真菌具有生理学上不同的抗性模式,并且其中至少一种伴有(1 <右箭头> 3)-β-葡聚糖酶诱导。

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