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克隆葡萄铬花叶线虫传多面体病毒的全长cDNA

Cloning full-length cDNA of grapevine chrome mosaic nepovirus.

作者信息

Le Gall O, Candresse T, Brault V, Bretout C, Hibrand L, Dunez J

机构信息

Station de Pathologie Végétale, INRA, Pont-de-la-Maye, France.

出版信息

Gene. 1988 Dec 15;73(1):67-75. doi: 10.1016/0378-1119(88)90313-7.

Abstract

Full-length cDNA copies of the genomic RNAs of grapevine chrome mosaic virus were obtained and cloned in Escherichia coli by a one-step procedure. The cloning protocol included size selections by agarose-gel electrophoresis of both the single-stranded and the double-stranded full-length cDNAs. First-strand cDNA synthesis was primed with oligodeoxythymidine while second-strand synthesis was primed with specific synthetic oligodeoxynucleotides, allowing cloning of the 3' poly(A) and of the last 5' nucleotides of the viral RNA template. For the 7.2-kb and 4.4-kb viral RNAs, up to 20% and 80%, respectively, of the clones were found to be full-length. Even for large templates, this procedure allows fast and efficient cloning of full-length cDNAs.

摘要

通过一步法获得了葡萄铬花叶病毒基因组RNA的全长cDNA拷贝,并将其克隆到大肠杆菌中。克隆方案包括通过琼脂糖凝胶电泳对单链和双链全长cDNA进行大小选择。第一链cDNA合成用寡聚脱氧胸苷引物,而第二链合成用特定的合成寡聚脱氧核苷酸引物,从而能够克隆病毒RNA模板的3'聚腺苷酸和最后的5'核苷酸。对于7.2kb和4.4kb的病毒RNA,分别发现高达20%和80%的克隆为全长。即使对于大模板,该方法也能快速高效地克隆全长cDNA。

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