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首页> 外文期刊>Turkish Journal of Agriculture & Forestry >Cloning, characterization, and expression of the gene encoding polygalacturonase- inhibiting proteins from strawberry
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Cloning, characterization, and expression of the gene encoding polygalacturonase- inhibiting proteins from strawberry

机译:草莓中聚半乳糖醛酸酶抑制蛋白编码基因的克隆,鉴定与表达

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摘要

Polygalacturonase-inhibiting proteins (PGIP) play important roles in the defense against plant pathogens, especially fungi. The sequence of strawberry PGIP gene was obtained using reverse transcription PCR (RT-PCR) and its expression in different tissues was studied by semi-quantitative RT-PCR. A cDNA fragment of FaPGIP gene was cloned and the sequence analysis shows that the fragment contains a full ORF of 999 bp encoding 332 amino acids. The FaPGIP gene from genomic DNA shows a single 168bp intron that is efficiently spliced out of the FaPGIP pre-mRNA transcript. The FaPGIP has a high degree of identity with previously isolated PGIP genes and the encoded polypeptide shows all the characteristic features of PGIP peptides. The 3 dimensional model of the protein contains 12 a -helices and 21 b -sheets, and the center LRR structural domain is composed of 10 tandem LRR motifs. The semi-quantitative RT-PCR revealed FaPGIP gene displaying high expression levels in fruit and leaf, middle expression in flower and root, and weak expression in stem. The expression level of FaPGIP gene is particular to tissues. Key words: Strawberry, polygalacturonase-inhibiting proteins (PGIP), cDNA cloning, tissue expression
机译:聚半乳糖醛酸酶抑制蛋白(PGIP)在防御植物病原体(尤其是真菌)中起着重要作用。利用逆转录PCR(RT-PCR)获得了草莓PGIP基因的序列,并通过半定量RT-PCR研究了其在不同组织中的表达。克隆了FaPGIP基因的cDNA片段,序列分析表明该片段包含一个999 bp的完整ORF,编码332个氨基酸。来自基因组DNA的FaPGIP基因显示单个168bp内含子,该内含子可以有效地从FaPGIP mRNA转录前剪接出来。 FaPGIP与先前分离的PGIP基因具有高度同一性,并且编码的多肽显示PGIP肽的所有特征。该蛋白质的3维模型包含12个a螺旋和21个b折叠,并且中心LRR结构域由10个串联LRR基序组成。半定量RT-PCR显示FaPGIP基因在果实和叶片中高表达,在花和根中高表达,在茎中低表达。 FaPGIP基因的表达水平特定于组织。关键词:草莓;聚半乳糖醛酸酶抑制蛋白(PGIP); cDNA克隆;组织表达

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