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鼠白血病病毒衣壳蛋白基因中的单氨基酸变化确定了Fv1抗性的靶点。

Single amino acid changes in the murine leukemia virus capsid protein gene define the target of Fv1 resistance.

作者信息

Kozak C A, Chakraborti A

机构信息

Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0460, USA.

出版信息

Virology. 1996 Nov 15;225(2):300-5. doi: 10.1006/viro.1996.0604.

Abstract

The mouse Fv1 genetic locus controls resistance to subgroups of ecotropic, MCF, and amphotropic murine leukemia viruses (MuLVs). In addition to the four previously defined alleles of Fv1 (Fv1(n), Fv1(b), Fv1(nr), Fv1(0)), we present evidence that the novel restriction pattern characteristic of DBA/2J mice maps to the Fv1 locus and therefore represents a novel allele, here designated Fv1(d). Previous studies had demonstrated that the Fv1-mediated viral tropism is determined within the capsid protein gene, and that N- and B-tropic virus capsids differ only in two adjacent amino acids. We introduced various amino acid substitutions at these two sites in the N-tropic AKV MLV capsid gene, and typed resulting viruses for host range on cells carrying all five Fv1 alleles as well as on cells from additional wild mouse species with Fv1-like differences in virus susceptibility. Results indicate that alteration of the first of the two amino acids does not alter tropism, but alteration of the second alone is sufficient to convert the N-tropic AKV MLV to a B-tropic virus. Substitution of leucine for arginine at this site produced a virus with an unusual tropism not characteristic of any of the naturally occurring or laboratory strains of MuLV.

摘要

小鼠Fv1基因位点控制对亲嗜性、MCF和兼嗜性鼠白血病病毒(MuLVs)亚组的抗性。除了先前定义的Fv1的四个等位基因(Fv1(n)、Fv1(b)、Fv1(nr)、Fv1(0))外,我们还提供证据表明,DBA/2J小鼠特有的新限制模式定位于Fv1基因位点,因此代表一个新的等位基因,这里命名为Fv1(d)。先前的研究表明,Fv1介导的病毒嗜性由衣壳蛋白基因决定,且N嗜性和B嗜性病毒衣壳仅在两个相邻氨基酸上存在差异。我们在N嗜性AKV MLV衣壳基因的这两个位点引入了各种氨基酸替换,并对产生的病毒在携带所有五个Fv1等位基因的细胞以及来自病毒易感性具有Fv1样差异的其他野生小鼠物种的细胞上进行宿主范围分型。结果表明,两个氨基酸中的第一个氨基酸的改变不会改变嗜性,但仅第二个氨基酸的改变就足以将N嗜性AKV MLV转化为B嗜性病毒。在该位点用亮氨酸替换精氨酸产生了一种具有异常嗜性的病毒,这种嗜性并非任何天然存在的或实验室的MuLV菌株所具有。

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