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一种通过限制酶切位点重建进行DNA片段亚克隆的通用方法:应用于对加兹达尔鼠肉瘤病毒转化基因的氨基末端编码区进行测序

A generalized method of subcloning DNA fragments by restriction site reconstruction: application to sequencing the amino-terminal coding region of the transforming gene of Gazdar murine sarcoma virus.

作者信息

Donoghue D J, Hunter T

出版信息

Nucleic Acids Res. 1982 Apr 24;10(8):2549-64. doi: 10.1093/nar/10.8.2549.

Abstract

The technique of restriction site reconstruction was generalized so as to allow the subcloning of any DNA fragment and its subsequent reexcision with EcoRI, XbaI, XhoI or HindIII. After excision, the 3' terminus of each strand will be derived from the starting nucleic acid, permitting the use of such fragments as primers for nucleotide sequencing by primer extension methods. The technique was used to subclone a 56 base pair BstNI-DdeI fragment of Moloney murine sarcoma virus (Mo-MSV) as a unique HindIII-HindIII fragment. This fragment then served as a primer to sequence a portion of the RNA genome of Gazdar murine sarcoma virus (Gz-MSV). The nucleotide sequence which was obtained indicated that the transforming gene of Gz-MSV arose by at least two recombination events involving murine leukemia virus (MLV) and the cellular homologue c-mos. This analysis suggests that a virus indistinguishable from Mo-MSV was an intermediate in the formation of Gz-MSV.

摘要

限制酶切位点重建技术得到了推广,以便能够亚克隆任何DNA片段,并随后用EcoRI、XbaI、XhoI或HindIII进行再次切割。切割后,每条链的3'末端将源自起始核酸,从而允许将此类片段用作引物,通过引物延伸法进行核苷酸测序。该技术用于将莫洛尼鼠肉瘤病毒(Mo-MSV)的一个56碱基对的BstNI-DdeI片段亚克隆为一个独特的HindIII-HindIII片段。然后,该片段用作引物,对加兹达尔鼠肉瘤病毒(Gz-MSV)的RNA基因组的一部分进行测序。获得的核苷酸序列表明,Gz-MSV的转化基因至少通过涉及鼠白血病病毒(MLV)和细胞同源物c-mos的两次重组事件产生。该分析表明,一种与Mo-MSV无法区分的病毒是Gz-MSV形成过程中的中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0385/320633/ee315ed0cf34/nar00377-0072-a.jpg

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