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FBR小鼠骨肉瘤病毒。I. 一种75,000道尔顿的gag-fos融合产物的分子分析与特性鉴定

FBR murine osteosarcoma virus. I. Molecular analysis and characterization of a 75,000-Da gag-fos fusion product.

作者信息

Curran T, Verma I M

出版信息

Virology. 1984 May;135(1):218-28. doi: 10.1016/0042-6822(84)90132-6.

Abstract

The FBR murine osteosarcoma virus complex induces bone tumors with a similar latency and pathology to those induced by the FBJ virus complex. FBR murine sarcoma virus ( FBR -MSV) has been isolated from its helper virus(es) by the establishment of transformed nonproducer cells. These cells were found to express a 75,000-Da protein (P75) which was antigenically related to the p55 oncogene product of the FBJ murine osteosarcoma virus ( FBJ -MSV). P75 also contained antigenic determinants of murine leukemia virus (MLV) gag gene p15, p12, and p30 proteins, and is therefore a gag- fos fusion protein ( P75gag - fos ). P75gag - fos is a phosphoprotein and is found primarily in the nucleus. Only a single species of RNA, of 3.3 kb, was identified in FBR -MSV-transformed nonproducer cells using both fos and MLV probes, which suggested that P75gag - fos was expressed from genome-sized RNA. Chromosomal DNA from one nonproducer cell line was found to contain a single EcoRI restriction fragment of 12 kb pairs (kbp) which encompassed the FBR -MSV provirus. This DNA fragment was molecularly cloned into bacteriophage Charon 30 (lambda FBR -1), and a 7.5-kbp HindIII restriction fragment containing the entire provirus was subsequently subcloned into pBR322 ( pFBR -1). DNA from pFBR -1 was capable of inducing morphological transformation of mouse and rat fibroblasts in tissue culture. In addition, transfected cells expressed the FBR -MSV P75gag - fos protein.

摘要

FBR小鼠骨肉瘤病毒复合体诱发的骨肿瘤,其潜伏期和病理与FBJ病毒复合体诱发的相似。通过建立转化的非生产性细胞,已从其辅助病毒中分离出FBR小鼠肉瘤病毒(FBR -MSV)。发现这些细胞表达一种75,000道尔顿的蛋白质(P75),该蛋白质与FBJ小鼠骨肉瘤病毒(FBJ -MSV)的p55癌基因产物具有抗原相关性。P75还含有鼠白血病病毒(MLV)gag基因p15、p12和p30蛋白的抗原决定簇,因此是一种gag - fos融合蛋白(P75gag - fos)。P75gag - fos是一种磷蛋白,主要存在于细胞核中。使用fos和MLV探针在FBR -MSV转化的非生产性细胞中仅鉴定出一种3.3 kb的RNA,这表明P75gag - fos是从基因组大小的RNA表达的。发现来自一个非生产性细胞系的染色体DNA含有一个12 kb对(kbp)的单一EcoRI限制片段,该片段包含FBR -MSV前病毒。该DNA片段被分子克隆到噬菌体Charon 30(λFBR -1)中,随后将包含整个前病毒的7.5-kbp HindIII限制片段亚克隆到pBR322(pFBR -1)中。来自pFBR -1的DNA能够在组织培养中诱导小鼠和大鼠成纤维细胞的形态转化。此外,转染的细胞表达FBR -MSV P75gag - fos蛋白。

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