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H-rev107基因的消减克隆,该基因在对H-ras有抗性的成纤维细胞中特异性表达。

Subtraction cloning of H-rev107, a gene specifically expressed in H-ras resistant fibroblasts.

作者信息

Hajnal A, Klemenz R, Schäfer R

机构信息

Department of Pathology, University of Zürich, Switzerland.

出版信息

Oncogene. 1994 Feb;9(2):479-90.

PMID:8290259
Abstract

We have isolated by subtractive hybridization a novel gene, called H-rev107, which is specifically expressed in a phenotypic revertant of H-ras transformed 208F rat fibroblasts. Apart from oncogene revertants, strong expression of H-rev107 was found in REF52 and EK-3 cells, two fibroblast lines resistant to transformation by activated H-ras oncogenes. In contrast, transformation-sensitive fibroblasts like 208F or NIH3T3 cells expressed only very little H-rev107 RNA. In H-ras or v-src transformed fibroblasts, H-rev107 RNA was undetectable. Introduction of the adenovirus E1A nuclear oncogene into ras-resistant REF52 cells abolished their transformation resistance and repressed the H-rev107 gene. H-rev107 encodes a protein with a molecular weight of 18 kDa without any structural similarity to known proteins. p18H-rev107 exists in two forms which can be distinguished by their electrophoretic mobility; one is localized predominantly in cell membranes, the other in the cytoplasm. In confluent contact-inhibited 208F cells, p18H-rev107 accumulated in cell membranes, while growth arrest induced by serum starvation did not induce H-rev107. In REF52, cell density had no influence on the expression or localization of p18H-rev107. Repression of the H-rev107 gene may be closely associated with the loss of density-dependent growth inhibition and with the expression of the neoplastic phenotype.

摘要

我们通过消减杂交分离出一个名为H-rev107的新基因,该基因在H-ras转化的208F大鼠成纤维细胞的表型回复突变体中特异性表达。除了癌基因回复突变体,在REF52和EK-3细胞中也发现了H-rev107的强表达,这两种成纤维细胞系对活化的H-ras癌基因转化具有抗性。相比之下,像208F或NIH3T3细胞这样对转化敏感的成纤维细胞仅表达极少量的H-rev107 RNA。在H-ras或v-src转化的成纤维细胞中,无法检测到H-rev107 RNA。将腺病毒E1A核癌基因导入对ras有抗性的REF52细胞中,消除了它们的转化抗性并抑制了H-rev107基因。H-rev107编码一种分子量为18 kDa的蛋白质,与已知蛋白质没有任何结构相似性。p18H-rev107以两种形式存在,可通过它们的电泳迁移率区分;一种主要定位于细胞膜,另一种定位于细胞质。在汇合接触抑制的208F细胞中,p18H-rev107在细胞膜中积累,而血清饥饿诱导的生长停滞并未诱导H-rev107。在REF52中,细胞密度对p18H-rev107的表达或定位没有影响。H-rev107基因的抑制可能与密度依赖性生长抑制的丧失以及肿瘤表型的表达密切相关。

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