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首页> 外文期刊>Biotechnology & Biotechnological Equipment >Cloning and allelic variation of two novel catalase genes ( SoCAT-1 and SsCAT-1 ) in Saccharum officinarum L. and Saccharum spontaneum L.
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Cloning and allelic variation of two novel catalase genes ( SoCAT-1 and SsCAT-1 ) in Saccharum officinarum L. and Saccharum spontaneum L.

机译:蔗糖和自发蔗糖中两个新过氧化氢酶基因(SoCAT-1和SsCAT-1)的克隆及其等位变异。

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摘要

Catalases (CAT) play important roles in plant defence mechanisms, stress response, cellular redox balance and aging delay. In order to clone CAT genes in cultivated ( Saccharum officinarum L.) and wild ( S. spontaneum L.) sugarcane, we designed two pairs of specific primers using a full length cDNA sequence of sorghum CAT gene (XM 002437586.1) as the probe. Two novel full-length sequences of CAT genes ( SoCAT-1 in S. officinarum and SsCAT-1 in S. spontaneum ) were cloned by nested polymerase chain reaction. Two allelic variants were found at SoCAT-1 ( SoCAT-1a and SoCAT-1b , GenBank accession nos. KF864224-25) and SsCAT-1 ( SsCAT-1a and SsCAT-1b , GenBank accession nos. KF864226-27) loci. The full lengths of SoCAT-1a, SoCAT-1b, SsCAT-1a and SsCAT-1b were 3816 bp, 3814 bp, 3777 bp and 3812 bp, respectively, and all contained eight exons and seven introns, with a similar gene structure. The length of cDNA for all four genes was 1532 bp, containing 10 bp 5'-untranslated region (UTR) and 43 bp 3'-UTR, and an open reading frame of 1479 bp encoding a polypeptide of 492 amino acids. High homology of DNA (99.0% for SoCAT-1 , 98.2% for SsCAT-1 ) and cDNA (99.3% for SoCAT-1 , 99.4% for SsCAT-1 ) were found. Eleven single nucleotide polymorphisms were found in cDNA SoCAT-1 and nine ones in SsCAT-1 , and nine and five amino-acid mutation sites in the predicted proteins, respectively. The predicted proteins encoded by SoCAT-1 and SsCAT-1 showed high homology with CAT in sorghum, rice, corn and other species.
机译:过氧化氢酶(CAT)在植物防御机制,胁迫响应,细胞氧化还原平衡和衰老延迟中起重要作用。为了在栽培的(Saccharum officinarum L.)和野生的(S.spontaneum L.)甘蔗中克隆CAT基因,我们使用高粱CAT基因的全长cDNA序列(XM 002437586.1)作为探针设计了两对特异性引物。通过巢式聚合酶链反应,克隆了两种新的CAT基因全长序列(S.officinarum中的SoCAT-1和S.stantaneum中的SsCAT-1)。在SoCAT-1(SoCAT-1a和SoCAT-1b,GenBank登录号为KF864224-25)和SsCAT-1(SsCAT-1a和SsCAT-1b,GenBank登录号为KF864226-27)的基因座上发现了两个等位基因变体。 SoCAT-1a,SoCAT-1b,SsCAT-1a和SsCAT-1b的全长分别为3816 bp,3814 bp,3777 bp和3812 bp,均包含八个外显子和七个内含子,具有相似的基因结构。所有四个基因的cDNA长度为1532 bp,包含10 bp 5'-非翻译区(UTR)和43 bp 3'-UTR,以及1479 bp的开放阅读框,编码492个氨基酸。发现了DNA(SoCAT-1为99.0%,SsCAT-1为98.2%)和cDNA(SoCAT-1为99.3%,SsCAT-1为99.4%)具有高度同源性。在cDNA SoCAT-1中发现了11个单核苷酸多态性,在SsCAT-1中发现了9个单核苷酸多态性,在预测的蛋白质中分别发现了9个和5个氨基酸突变位点。 SoCAT-1和SsCAT-1编码的预测蛋白在高粱,水稻,玉米和其他物种中与CAT具有高度同源性。

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