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Construction of a cDNA library from female adult of Toxocara canis, and analysis of EST and immune-related genes expressions

机译:犬弓形虫成年女性cDNA文库的构建及EST及免疫相关基因表达分析

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Toxocara canis is a widespread intestinal nematode parasite of dogs, which can also cause disease in humans. We employed an expressed sequence tag (EST) strategy in order to study gene-expression including development, digestion and reproduction of T. canis. ESTs provided a rapid way to identify genes, particularly in organisms for which we have very little molecular information. In this study, a cDNA library was constructed from a female adult of T. canis and 215 high-quality ESTs from 5'-ends of the cDNA clones representing 79 unigenes were obtained. The titer of the primary cDNA library was 1.83 x 10(6) pfu/mL with a recombination rate of 99.33%. Most of the sequences ranged from 300 to 900 bp with an average length of 656 bp. Cluster analysis of these ESTs allowed identification of 79 unique sequences containing 28 contigs and 51 singletons. BLASTX searches revealed that 18 unigenes (22.78% of the total) or 70 ESTs (32.56% of the total) were novel genes that had no significant matches to any protein sequences in the public databases. The rest of the 61 unigenes (77.22% of the total) or 145 ESTs (67.44% of the total) were closely matched to the known genes or sequences deposited in the public databases. These genes were classified into seven groups based on their known or putative biological functions. We also confirmed the gene expression patterns of several immune-related genes using RT-PCR examination. This work will provide a valuable resource for the further investigations in the stage-, sex- and tissue-specific gene transcription or expression
机译:犬弓形虫是狗的一种广泛的肠道线虫寄生虫,也可能导致人类疾病。为了研究基因表达,包括犬小肠球菌的发育,消化和繁殖,我们采用了表达序列标签(EST)策略。 ESTs提供了一种鉴定基因的快速方法,特别是在我们缺乏分子信息的生物中。在这项研究中,从雌性成年犬T. canis构建了一个cDNA文库,并从代表79个单基因的cDNA克隆的5'端获得了215个高质量的EST。初级cDNA文库的滴度为1.83 x 10(6)pfu / mL,重组率为99.33%。大多数序列范围为300至900 bp,平均长度为656 bp。这些EST的聚类分析允许鉴定包含28个重叠群和51个单例的79个独特序列。 BLASTX搜索显示18个单基因(占总数的22.78%)或70个EST(占总数的32.56%)是与公共数据库中的任何蛋白质序列均无显着匹配的新基因。 61个单基因的其余部分(占总数的77.22%)或145个EST(占总数的67.44%)与公共数据库中存放的已知基因或序列紧密匹配。根据它们的已知或假定的生物学功能,将这些基因分为七个组。我们还使用RT-PCR检查确认了几种免疫相关基因的基因表达模式。这项工作将为进一步研究阶段,性别和组织特异性基因转录或表达提供有价值的资源

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