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Identification of the pepper SAR8.2 gene as a molecular marker for pathogen infection, abiotic elicitors and environmental stresses in Capsicum annuum

机译:辣椒SAR8.2基因鉴定为辣椒中病原体感染,非生物激发子和环境胁迫的分子标记

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Pepper (Capsicum annuum L.) SAR8.2 genes, designated CASAR82A, B and C, which are induced by all the biotic and abiotic stresses, were isolated from a pepper cDNA library constructed with the mRNAs from pepper plants infected with Xanthomonas campestris pv. vesicatoria. The pepper CASAR82A, B and C gene products, which are very similar to each other in amino acid sequences, have 43–50% homology with those of tobacco SAR8.2 genes. The CASAR8.2 genes were not constitutively expressed in any of the organs of healthy pepper plants. In contrast, the CASAR82A gene was locally or systemically induced in pepper plants infected by X. campestris pv. vesicatoria, Colletotrichum coccodes or Phytophthora capsici. Strong induction of the CASAR82A gene also was found in pepper leaves treated with ethylene, methyl jasmonate, indole-3-acetic acid, abscisic acid, salicylic acid, benzothiadiazole, DL-β-n-amino butyric acid or hydrogen peroxide. Interestingly, the transcription of the CASAR82A gene was rapidly triggered by high salinity, drought or low-temperature stresses, but not by mechanical wounding. In situ hybridization results revealed that the CASAR82A mRNAs were localized in phloem and epidermal cells of pepper leaf and stem tissues infected by C. coccodes and P. capsici, or treated with salicylic acid. These results thus suggest that pepper SAR8.2 genes may be valuable as a molecular marker for the detection of various pathogen infections, abiotic elicitors and environmental stresses.
机译:从由所有生物和非生物胁迫诱导的辣椒(Capsicum annuum L.)SAR8.2基因中,从由受到Xanthomonas campestris pv感染的辣椒植物的mRNA构建的辣椒cDNA文库中分离,该基因由所有生物和非生物胁迫诱导。 vesicatoria。辣椒的CASAR82A,B和C基因产物在氨基酸序列上非常相似,与烟草SAR8.2基因具有43-50%的同源性。在健康辣椒植物的任何器官中均未组成性表达CASAR8.2基因。相比之下,CASAR82A基因是在被X. campestris pv感染的辣椒植物中局部或全身诱导的。 vesicatoria,Colletotrichum编码或辣椒疫霉。在用乙烯,茉莉酸甲酯,吲哚-3-乙酸,脱落酸,水杨酸,苯并噻二唑,DL-β-正氨基丁酸或过氧化氢处理的辣椒叶中也发现了CASAR82A基因的强诱导作用。有趣的是,高盐度,干旱或低温胁迫迅速触发了CASAR82A基因的转录,但机械损伤并未迅速触发。原位杂交结果表明,CASAR82A mRNAs定位于辣椒叶和茎组织的韧皮部和表皮细胞中,并被C. coccodes和辣椒辣椒感染,或用水杨酸处理。因此,这些结果表明,胡椒SAR8.2基因作为检测各种病原体感染,非生物诱因和环境胁迫的分子标记可能有价值。

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