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从豌豆根瘤mRNA中分离脂氧合酶cDNA克隆。

Isolation of lipoxygenase cDNA clones from pea nodule mRNA.

作者信息

Wisniewski J P, Gardner C D, Brewin N J

机构信息

John Innes Centre, Norwich, UK.

出版信息

Plant Mol Biol. 1999 Mar;39(4):775-83. doi: 10.1023/a:1006184516754.

Abstract

The pattern of lipoxygenase (LOX) gene expression was investigated in pea nodule tissues using the technique of in situ hybridization. Five lipoxygenase cDNAs were cloned from nodule mRNA by the RT-PCR and 3' RACE procedures. These clones (loxN1 to loxN5) show a high degree of sequence homology, except in the 3'-untranslated region. Gene-specific riboprobes were therefore generated from subclones carrying the 3'-untranslated regions in order to investigate tissue-specific gene expression. Northern blotting analysis revealed that loxN1 corresponded to a transcript that was expressed exclusively in roots and nodules but not in the aerial parts of the plant. However, none of the LOX genes appeared to be up-regulated in nodule tissue relative to uninfected roots. Starting with the incomplete cDNA clone for loxN1, the full coding sequence termed lox1:P.s:1 was obtained by further rounds of RT-PCR and 5' RACE procedures. In situ hybridization with nodule tissues revealed several different patterns of expression for the various LOX probes. However, none of the corresponding transcripts was expressed exclusively in the invasion zone, as might have been expected if one LOX gene product had been uniquely associated with the invasion process. In conclusion, this study provides no evidence for a direct role for any LOX gene product in plant-microbe interaction or host defence, but the fact that all the transcripts were expressed at the nodule apex suggests that LOX could be involved in the development of this organ.

摘要

利用原位杂交技术研究了豌豆根瘤组织中脂氧合酶(LOX)基因的表达模式。通过逆转录聚合酶链反应(RT-PCR)和3'端快速扩增cDNA末端(3' RACE)程序,从根瘤信使核糖核酸(mRNA)中克隆出5个脂氧合酶cDNA。这些克隆(loxN1至loxN5)除了在3'非翻译区外,显示出高度的序列同源性。因此,从携带3'非翻译区的亚克隆中生成了基因特异性核糖探针,以研究组织特异性基因表达。Northern印迹分析表明,loxN1对应于一种仅在根和根瘤中表达而不在植物地上部分表达的转录本。然而,相对于未感染的根,没有一个LOX基因在根瘤组织中上调表达。从loxN1的不完整cDNA克隆开始,通过进一步的RT-PCR和5' RACE程序获得了称为lox1:P.s:1的完整编码序列。与根瘤组织的原位杂交揭示了各种LOX探针的几种不同表达模式。然而,没有一个相应的转录本仅在侵入区表达,而如果有一种LOX基因产物与侵入过程唯一相关,情况可能就是这样。总之,本研究没有提供任何证据表明任何LOX基因产物在植物-微生物相互作用或宿主防御中起直接作用,但所有转录本都在根瘤顶端表达这一事实表明,LOX可能参与了该器官的发育。

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