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鼠γ-疱疹病毒68编码胸苷激酶和糖蛋白H的同源物:嘧啶激酶活性的序列、表达及特性分析

Murine gammaherpesvirus-68 encodes homologues of thymidine kinase and glycoprotein H: sequence, expression, and characterization of pyrimidine kinase activity.

作者信息

Pepper S D, Stewart J P, Arrand J R, Mackett M

机构信息

CRC Department of Molecular Biology, Paterson Institute for Cancer Research, Christie CRC Research Centre, Christie Hospit, Withington, Manchester, United Kingdom.

出版信息

Virology. 1996 May 15;219(2):475-9. doi: 10.1006/viro.1996.0274.

Abstract

We have sequenced a 4.5-kb fragment of DNA spanning the junction of the BamHI D and E fragments of murine gammaherpesvirus-68 (MHV-68). This sequence was found to code for two major open reading frames (orfs) of 1934 and 2192 bp which showed significant homology to the thymidine kinase (TK) and glycoprotein H (gH) sequences of other gammaherpesviruses. Upstream from the TK gene another orf was found which showed amino acid sequence homology to the HSV1 UL24 gene. Analysis of the 1934-bp orf revealed the presence of all six of the recognized sites that are conserved between herpesvirus TKs although, uniquely among sequenced herpesvirus TK enzymes, MHV-68 lacks the consensus nucleotide binding site GXXGXGK, the second glycine being replaced by alanine. The MHV-68 TK has a predicted M(r) of 68,443, while the gH is predicted to have a M(r) of 82,890. Northern blot analysis showed an early TK message of 2.6 kb and a late gH-specific message of 2.5 kb. Both TK and gH probes detected a 4.3-kb late message, implying that this late message spans gH and TK. The TK coding sequence was expressed using an in vitro transcription translation system and was shown to encode functional TK activity.

摘要

我们对一段4.5kb的DNA片段进行了测序,该片段跨越鼠γ疱疹病毒68(MHV - 68)的BamHI D和E片段的连接处。发现该序列编码两个主要的开放阅读框(orfs),长度分别为1934bp和2192bp,它们与其他γ疱疹病毒的胸苷激酶(TK)和糖蛋白H(gH)序列具有显著同源性。在TK基因上游发现了另一个orf,其氨基酸序列与HSV1 UL24基因同源。对1934bp的orf分析表明,疱疹病毒TK之间保守的所有六个公认位点均存在,不过,在已测序的疱疹病毒TK酶中,MHV - 68独特地缺乏共有核苷酸结合位点GXXGXGK,第二个甘氨酸被丙氨酸取代。MHV - 68 TK的预测分子量为68,443,而gH的预测分子量为82,890。Northern印迹分析显示,有一个2.6kb的早期TK信使RNA和一个2.5kb的晚期gH特异性信使RNA。TK和gH探针均检测到一个4.3kb的晚期信使RNA,这意味着该晚期信使RNA跨越gH和TK。使用体外转录翻译系统表达了TK编码序列,并证明其编码功能性TK活性。

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