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劳斯氏肉瘤病毒膜糖蛋白基因突变导致致白血病性降低。

Reduced leukemogenicity caused by mutations in the membrane glycoprotein gene of Rauscher spleen focus-forming virus.

作者信息

Machida C A, Bestwick R K, Kabat D

出版信息

J Virol. 1984 Feb;49(2):394-402. doi: 10.1128/JVI.49.2.394-402.1984.

Abstract

We isolated and characterized two spontaneous, weakly leukemogenic mutants of Rauscher spleen focus-forming virus (R-SFFV) that contain mutations in nonoverlapping regions of the membrane envelope (env) glycoprotein gene. As reported previously (M. Ruta and D. Kabat, J. Virol. 35:844-853, 1980), the replication-defective R-SFFV encodes a membrane glycoprotein with an apparent Mr of 54,000 (gp54) which is structurally and immunologically related to the membrane envelope glycoproteins of dual-tropic murine leukemia viruses. Mutant R-SFFV clones 3-25 and 4-3 encode abnormally sized gp54-related glycoproteins with apparent Mrs of 52,000 (gp52) and 45,000 (gp45), respectively. Northern and Southern blot analyses of the mutant R-SFFV nucleic acids indicated that an insertion has occurred in the 3-25 env gene and that a deletion has occurred in the 4-3 env gene. Furthermore, restriction endonuclease analyses and comparisons of the fragmentation patterns of the wild-type and mutant glycoproteins generated by partial proteolysis with Staphylococcus aureus V8 protease indicated that the mutations affect nonoverlapping domains of the envelope glycoprotein (amino-terminal fragment affected in 3-25 glycoprotein and carboxyl-terminal fragment affected in 4-3 glycoprotein). Glycosylation inhibition studies indicated that the reduced size of gp52 is caused at least partly by loss of an asparagine-linked oligosaccharide. In addition, these mutant viruses have dramatically reduced leukemogenicities compared with wild-type R-SFFV. We conclude that the gp54 structural gene is required for initiation or amplification of the splenic erythroblast hyperplasia which characterizes the preleukemic phase of Rauscher disease.

摘要

我们分离并鉴定了劳舍尔脾脏病灶形成病毒(R-SFFV)的两个自发的、弱致白血病突变体,它们在膜包膜(env)糖蛋白基因的非重叠区域含有突变。如先前报道(M. Ruta和D. Kabat,《病毒学杂志》35:844 - 853,1980),复制缺陷型R-SFFV编码一种表观分子量为54,000的膜糖蛋白(gp54),其在结构和免疫上与双嗜性鼠白血病病毒的膜包膜糖蛋白相关。突变型R-SFFV克隆3 - 25和4 - 3分别编码大小异常的与gp54相关的糖蛋白,表观分子量分别为52,000(gp52)和45,000(gp45)。对突变型R-SFFV核酸的Northern和Southern印迹分析表明,3 - 25 env基因发生了插入,4 - 3 env基因发生了缺失。此外,用金黄色葡萄球菌V8蛋白酶进行部分蛋白水解产生的野生型和突变型糖蛋白片段模式的限制性内切酶分析和比较表明,这些突变影响包膜糖蛋白的非重叠结构域(3 - 25糖蛋白中受影响的氨基末端片段和4 - 3糖蛋白中受影响的羧基末端片段)。糖基化抑制研究表明,gp52大小的减小至少部分是由于天冬酰胺连接的寡糖的丢失。此外,与野生型R-SFFV相比,这些突变病毒的致白血病性显著降低。我们得出结论,gp54结构基因是启动或扩增脾脏成红细胞增生所必需的,而脾脏成红细胞增生是劳舍尔病白血病前期的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/370e/255478/93bd2a5963b8/jvirol00137-0101-a.jpg

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