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弗瑞德白血病病毒的宿主限制:宿主范围变体的 gag 蛋白

Host restriction of Friend leukemia virus: gag proteins of host range variants.

作者信息

Duttagupta S, Soeiro R

出版信息

Proc Natl Acad Sci U S A. 1981 Apr;78(4):2320-4. doi: 10.1073/pnas.78.4.2320.

Abstract

The host response to murine ecotropic leukemia viruses is mainly controlled by the mouse Fv-1 gene. This locus controls virus replication at an intracellular stage and prevents provirus integration. Biological studies suggest that the Fv-1 effector molecule recognizes at least one virion structural protein. We have produced host range variants of B-tropic Friend murine leukemia virus in order to study the primary structure of potential viral target proteins. Our results show that conversion of B-tropism to NB-tropism is associated with changes in the primary structure of three gag proteins--p15, p12, and p30. These results suggest that host range conversion is due to a recombinational event, presumably between the parental virus and an endogenous murine virus. They also open the possibility that p12 and p30 may be involved in host range restriction.

摘要

宿主对鼠嗜亲性白血病病毒的反应主要由小鼠Fv-1基因控制。该基因座在细胞内阶段控制病毒复制,并阻止前病毒整合。生物学研究表明,Fv-1效应分子识别至少一种病毒粒子结构蛋白。为了研究潜在病毒靶蛋白的一级结构,我们制备了B嗜性Friend鼠白血病病毒的宿主范围变体。我们的结果表明,B嗜性向NB嗜性的转变与三种gag蛋白——p15、p12和p30的一级结构变化有关。这些结果表明,宿主范围的转变是由于重组事件,推测发生在亲代病毒和内源性鼠病毒之间。它们还开启了p12和p30可能参与宿主范围限制的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7499/319337/de5f96059e24/pnas00655-0364-a.jpg

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