Suppr超能文献

劳斯肉瘤病毒部分转化突变体感染细胞中的转化参数及pp60src定位

Transformation parameters and pp60src localization in cells infected with partial transformation mutants of Rous sarcoma virus.

作者信息

Rohrschneider L, Rosok M J

出版信息

Mol Cell Biol. 1983 Apr;3(4):731-46. doi: 10.1128/mcb.3.4.731-746.1983.

Abstract

Rous sarcoma virus (RSV)-induced transformation is mediated by the action of the viral src gene product pp60src. This transforming protein is found at several cytoplasmic locations, including the adhesion plaques of RSV-transformed cells. In these studies, we have focused on the adhesion plaque location of pp60src and determined whether any of the induced transformation parameters correlate with the presence of pp60src in the adhesion plaques. A series of partial transformation mutants of RSV that induce distinct transformation phenotypes were used, and infected chicken embryo cells were examined for (i) intracellular pp60src location, (ii) vinculin localization, (iii) abundance of phosphotyrosine on vinculin, (iv) integrity of stress fibers, and (v) expression of cell surface fibronectin. The results indicate that, among the limited number of mutants studied here, the presence of pp60src in adhesion plaques is independent of growth in soft agar and the increased phosphorylation of vinculin on tyrosine, but it does correlate with the loss of cell surface fibronectin. An elevated abundance of phosphotyrosine on vinculin is insufficient to cause stress fiber dissolution and is independent of the loss of fibronectin from the extracellular matrix. However, the increased relative amount of phosphotyrosine on vinculin is related to the ability of the cells to grow in soft agar. The adhesion plaque binding and tyrosine-specific kinase activities seem to represent two independent functions of pp60src.

摘要

劳氏肉瘤病毒(RSV)诱导的细胞转化是由病毒src基因产物pp60src的作用介导的。这种转化蛋白存在于几个细胞质位置,包括RSV转化细胞的黏着斑。在这些研究中,我们聚焦于pp60src在黏着斑的位置,并确定是否有任何诱导的转化参数与黏着斑中pp60src的存在相关。我们使用了一系列诱导不同转化表型的RSV部分转化突变体,并对感染的鸡胚细胞进行了以下检测:(i)细胞内pp60src的位置;(ii)纽蛋白的定位;(iii)纽蛋白上磷酸酪氨酸的丰度;(iv)应力纤维的完整性;(v)细胞表面纤连蛋白的表达。结果表明,在此研究的有限数量的突变体中,黏着斑中pp60src的存在与在软琼脂中的生长以及纽蛋白酪氨酸磷酸化增加无关,但它确实与细胞表面纤连蛋白的缺失相关。纽蛋白上磷酸酪氨酸丰度的升高不足以导致应力纤维溶解,并且与细胞外基质中纤连蛋白的缺失无关。然而,纽蛋白上磷酸酪氨酸相对量的增加与细胞在软琼脂中生长的能力有关。黏着斑结合和酪氨酸特异性激酶活性似乎代表了pp60src的两种独立功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7b2/368589/bf0f86aaebbe/molcellb00158-0246-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验