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Eicosapentaenoic and Arachidonic Acids from Phytophthora infestans Elicit Fungitoxic Sesquiterpenes in the Potato.疫霉脂肪酸激发马铃薯产生真菌毒性倍半萜
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Involvement of 3-hydroxy-3-methylglutaryl coenzyme a reductase in the regulation of sesquiterpenoid phytoalexin synthesis in potato.3-羟基-3-甲基戊二酰辅酶 A 还原酶在马铃薯倍半萜类植物抗毒素合成中的调控作用。
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Elicitor induction of mRNA activity. Rapid effects of elicitor on phenylalanine ammonia-lyase and chalcone synthase mRNA activities in bean cells.激发子诱导的mRNA活性。激发子对菜豆细胞中苯丙氨酸解氨酶和查尔酮合酶mRNA活性的快速影响。
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Mechanisms of inhibition by mevinolin (MK 803) of microsome-bound radish and of partially purified yeast HMG-CoA reductase (EC.1.1.1.34).美伐他汀(MK 803)对微粒体结合的萝卜和部分纯化的酵母HMG-CoA还原酶(EC.1.1.1.34)的抑制机制。
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Transcriptional activation of plant defense genes by fungal elicitor, wounding, and infection.真菌激发子、创伤和感染对植物防御基因的转录激活。
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创伤和病原体攻击对马铃薯3-羟基-3-甲基戊二酰辅酶A还原酶基因的差异激活作用

Differential activation of potato 3-hydroxy-3-methylglutaryl coenzyme A reductase genes by wounding and pathogen challenge.

作者信息

Yang Z, Park H, Lacy G H, Cramer C L

机构信息

Department of Plant Pathology, Physiology, and Weed Science, Virginia Polytechnic Institute and State University, Blacksburg 24061-0330.

出版信息

Plant Cell. 1991 Apr;3(4):397-405. doi: 10.1105/tpc.3.4.397.

DOI:10.1105/tpc.3.4.397
PMID:1840919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC160009/
Abstract

Potato genes encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR) were expressed in response to pathogen, elicitor, and wounding. HMGR catalyzes the rate-limiting step in isoprenoid biosynthesis leading to accumulation of phytoalexins and steroid glycoalkaloids. Wounding caused increases in HMGR mRNA levels. A rapid and transient peak occurred 30 minutes after wounding, followed by a slower peak at 14 hours; both were correlated with increased enzyme activity. Induction of HMGR mRNA by the soft rot pathogen Erwinia carotovora subsp carotovora or arachidonic acid began 8 hours after challenge and continued through 22 hours. Potato HMGR is encoded by a gene family. An HMGR gene-specific probe was used to demonstrate that one isogene of the HMGR family is pathogen activated and is distinct from isogene(s) that are wound activated. This provides evidence that defense-related increases in HMGR activity are due to mRNA level increases and that HMGR isogenes are activated differentially by wounding or pathogen challenge.

摘要

编码3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)的马铃薯基因在病原体、激发子和创伤刺激下表达。HMGR催化类异戊二烯生物合成中的限速步骤,导致植保素和甾体糖生物碱的积累。创伤导致HMGR mRNA水平升高。创伤后30分钟出现快速且短暂的峰值,随后在14小时出现较慢的峰值;两者均与酶活性增加相关。软腐病原菌胡萝卜软腐欧文氏菌胡萝卜亚种或花生四烯酸对HMGR mRNA的诱导在侵染后8小时开始,并持续至22小时。马铃薯HMGR由一个基因家族编码。使用HMGR基因特异性探针证明,HMGR家族的一个同基因被病原体激活,且与被创伤激活的同基因不同。这提供了证据,表明与防御相关的HMGR活性增加是由于mRNA水平升高,并且HMGR同基因在创伤或病原体侵染时被差异激活。