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多嗜性鼠白血病病毒(MLV)分离株的抗原亚类反映了NFS/N小鼠中内源性多嗜性MLV相关序列的三个不同组。

Antigenic subclasses of polytropic murine leukemia virus (MLV) isolates reflect three distinct groups of endogenous polytropic MLV-related sequences in NFS/N mice.

作者信息

Evans Leonard H, Lavignon Marc, Taylor Marc, Alamgir A S M

机构信息

Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840, USA.

出版信息

J Virol. 2003 Oct;77(19):10327-38. doi: 10.1128/jvi.77.19.10327-10338.2003.

Abstract

Polytropic murine leukemia viruses (MLVs) are generated by recombination of ecotropic MLVs with members of a family of endogenous proviruses in mice. Previous studies have indicated that polytropic MLV isolates comprise two mutually exclusive antigenic subclasses, each of which is reactive with one of two monoclonal antibodies termed MAb 516 and Hy 7. A major determinant of the epitopes distinguishing the subclasses mapped to a single amino acid difference in the SU protein. Furthermore, distinctly different populations of the polytropic MLV subclasses are generated upon inoculation of different ecotropic MLVs. Here we have characterized the majority of endogenous polytropic MLV-related proviruses of NFS/N mice. Most of the proviruses contain intact sequences encoding the receptor-binding region of the SU protein and could be distinguished by sequence heterogeneity within that region. We found that the endogenous proviruses comprise two major groups that encode the major determinant for Hy 7 or MAb 516 reactivity. The Hy 7-reactive proviruses correspond to previously identified polytropic proviruses, while the 516-reactive proviruses comprise the modified polytropic proviruses as well as a third group of polytropic MLV-related proviruses that exhibit distinct structural features. Phylogenetic analyses indicate that the latter proviruses reflect features of phylogenetic intermediates linking xenotropic MLVs to the polytropic and modified polytropic proviruses. These studies elucidate the relationships of the antigenic subclasses of polytropic MLVs to their endogenous counterparts, identify a new group of endogenous proviruses, and identify distinguishing characteristics of the proviruses that should facilitate a more precise description of their expression in mice and their participation in recombination to generate recombinant viruses.

摘要

多嗜性鼠白血病病毒(MLVs)是由嗜亲性MLVs与小鼠内源性前病毒家族的成员重组产生的。先前的研究表明,多嗜性MLV分离株包含两个相互排斥的抗原亚类,每个亚类都与两种单克隆抗体(称为单克隆抗体516和Hy 7)中的一种发生反应。区分这些亚类的表位的主要决定因素映射到SU蛋白中的单个氨基酸差异。此外,接种不同的嗜亲性MLVs会产生明显不同的多嗜性MLV亚类群体。在这里,我们对NFS/N小鼠的大多数内源性多嗜性MLV相关前病毒进行了表征。大多数前病毒包含编码SU蛋白受体结合区域的完整序列,并且可以通过该区域内的序列异质性来区分。我们发现内源性前病毒包括两个主要组,它们编码Hy 7或单克隆抗体516反应性的主要决定因素。Hy 7反应性前病毒对应于先前鉴定的多嗜性前病毒,而516反应性前病毒包括修饰的多嗜性前病毒以及第三组具有独特结构特征的多嗜性MLV相关前病毒。系统发育分析表明,后一种前病毒反映了将异嗜性MLVs与多嗜性和修饰的多嗜性前病毒联系起来的系统发育中间体的特征。这些研究阐明了多嗜性MLVs的抗原亚类与其内源性对应物之间的关系,鉴定了一组新的内源性前病毒,并确定了前病毒的区别特征,这将有助于更精确地描述它们在小鼠中的表达以及它们参与重组以产生重组病毒的情况。

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