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弗氏脾脏集落形成前病毒感染性克隆的完整核苷酸序列:gp55是一种包膜融合糖蛋白。

Complete nucleotide sequence of an infectious clone of Friend spleen focus-forming provirus: gp55 is an envelope fusion glycoprotein.

作者信息

Clark S P, Mak T W

出版信息

Proc Natl Acad Sci U S A. 1983 Aug;80(16):5037-41. doi: 10.1073/pnas.80.16.5037.

Abstract

The Friend spleen focus-forming provirus is 6,296 base pairs (bp) in length. Compared to Moloney murine leukemia virus, it has undergone five major deletions, three substitutions, and a number of minor alterations. Otherwise, these viruses are about 90% homologous. A 16-bp palindrome is found in the region thought to be involved in packaging and dimerization of the RNA genome. Premature termination of translation of the gag polyprotein is attributed to a 13-bp deletion in the p12 region. A substitution of xenotropic env sequences was identified in the 5' region of the env gene; 150 nucleotides 3' to this substitution, a deletion of 585 bp removes the site where the normal env precursor protein is cleaved to form gp70 and p15(E), resulting in a fusion protein of Mr 44,725. Due to these changes, the env product gp55 is expected to have a substantially different conformation on the cell surface compared to either a xenotropic or ecotropic gp70 protein, and may be responsible for the rapid erythroleukemic potential of spleen focus-forming virus.

摘要

Friend脾集落形成前病毒长度为6296个碱基对(bp)。与莫洛尼鼠白血病病毒相比,它经历了五次主要缺失、三次替换以及一些小的改变。除此之外,这些病毒约90%同源。在被认为与RNA基因组包装和二聚化有关的区域发现了一个16 bp的回文序列。gag多蛋白翻译的过早终止归因于p12区域的一个13 bp缺失。在env基因的5'区域鉴定出了异嗜性env序列的替换;在该替换位点下游3'端150个核苷酸处,一个585 bp的缺失去除了正常env前体蛋白被切割形成gp70和p15(E)的位点,导致产生一个分子量为44725的融合蛋白。由于这些变化,预计env产物gp55在细胞表面的构象与异嗜性或亲嗜性gp70蛋白相比有很大不同,并且可能是脾集落形成病毒快速致红白血病潜能的原因。

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