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与五种1型单纯疱疹病毒基因同源的牛2型疱疹病毒核苷酸序列的基因组定位。

Genomic location of bovid herpesvirus type 2 nucleotide sequences homologous to five herpes simplex virus type 1 genes.

作者信息

Yeung K C, d'Offay J, Oakes J E

机构信息

Department of Microbiology and Immunology, College of Medicine, University of South Alabama, Mobile 3668822.

出版信息

Virus Res. 1988 Jun;10(4):369-80. doi: 10.1016/0168-1702(88)90077-9.

Abstract

The location of nucleotide sequences within the bovid herpesvirus 1 (BHV-2) genome homologous to herpes simplex virus 1 (HSV-1) DNA were investigated. BHV-2 DNA was digested with restriction endonucleases and blotted to nitrocellulose paper. The blots were then probed with plasmids containing HSV-1 genes for thymidine kinase (TK), the major DNA binding protein (ICP8), the major capsid protein (VP5) and genes for HSV-1 glycoproteins gB, gD, and gC. Except for HSV-1 gC, each HSV-1 gene tested hybridized to BHV-2 nucleotide sequences that were located either on both sides of a restriction endonuclease cleavage site, within a small restriction endonuclease fragment, or to an area common to two overlapping restriction fragments. Thus, we were able to localize BHV-2 nucleotide sequences homologous to the HSV-1 ICP8 gene between 0.38 and 0.41 map units (m.u.), and BHV-2 nucleotide sequences homologous to the HSV-1 VP5 gene between 0.24 and 0.27 m.u. In addition, BHV-2 nucleotide sequences homologous to HSV-1 genes for TK, gB and gD were found to lie on both sides of restriction endonuclease cleavage sites at 0.30, 0.35, and 0.94 m.u., respectively.

摘要

对牛疱疹病毒1型(BHV - 2)基因组中与单纯疱疹病毒1型(HSV - 1)DNA同源的核苷酸序列的位置进行了研究。用限制性内切酶消化BHV - 2 DNA,并将其印迹到硝酸纤维素纸上。然后用含有HSV - 1胸苷激酶(TK)基因、主要DNA结合蛋白(ICP8)基因、主要衣壳蛋白(VP5)基因以及HSV - 1糖蛋白gB、gD和gC基因的质粒对印迹进行杂交检测。除HSV - 1 gC外,所检测的每个HSV - 1基因均与位于限制性内切酶切割位点两侧、小的限制性内切酶片段内或两个重叠限制性片段共有的区域的BHV - 2核苷酸序列杂交。因此,我们能够将与HSV - 1 ICP8基因同源的BHV - 2核苷酸序列定位在0.38至0.41个图距单位(m.u.)之间,将与HSV - 1 VP5基因同源的BHV - 2核苷酸序列定位在0.24至0.27 m.u.之间。此外,发现与HSV - 1的TK、gB和gD基因同源的BHV - 2核苷酸序列分别位于0.30、0.35和0.94 m.u.的限制性内切酶切割位点两侧。

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