Yarden Y, Kuang W J, Yang-Feng T, Coussens L, Munemitsu S, Dull T J, Chen E, Schlessinger J, Francke U, Ullrich A
Department of Developmental Biology, Genentech, Inc., South San Francisco 94080.
EMBO J. 1987 Nov;6(11):3341-51. doi: 10.1002/j.1460-2075.1987.tb02655.x.
Structural features of v-kit, the oncogene of HZ4 feline sarcoma virus, suggested that this gene arose by transduction and truncation of cellular sequences. Complementary DNA cloning of the human proto-oncogene coding for a receptor tyrosine kinase confirmed this possibility: c-kit encodes a transmembrane glycoprotein that is structurally related to the receptor for macrophage growth factor (CSF-1) and the receptor for platelet-derived growth factor. The c-kit gene is widely expressed as a single, 5-kb transcript, and it is localized to human chromosome 4 and to mouse chromosome 5. A c-kit peptide antibody permitted the identification of a 145,000 dalton c-kit gene product that is inserted in the cellular plasma membrane and is capable of self-phosphorylation on tyrosine residues in both human glioblastoma cells and transfected mouse fibroblasts. Our results suggest that p145c-kit functions as a cell surface receptor for an as yet unidentified ligand. Furthermore, carboxy- and amino-terminal truncations that occurred during the viral transduction process are likely to have generated the transformation potential of v-kit.
HZ4猫肉瘤病毒的致癌基因v-kit的结构特征表明,该基因是通过细胞序列的转导和截短产生的。编码受体酪氨酸激酶的人类原癌基因的互补DNA克隆证实了这种可能性:c-kit编码一种跨膜糖蛋白,其结构与巨噬细胞生长因子(CSF-1)受体和血小板衍生生长因子受体相关。c-kit基因以单一的5kb转录本广泛表达,它定位于人类4号染色体和小鼠5号染色体。一种c-kit肽抗体能够鉴定出一种145,000道尔顿的c-kit基因产物,该产物插入细胞质膜,并且在人类胶质母细胞瘤细胞和转染的小鼠成纤维细胞中都能够在酪氨酸残基上进行自我磷酸化。我们的结果表明,p145c-kit作为一种尚未确定配体的细胞表面受体发挥作用。此外,病毒转导过程中发生的羧基末端和氨基末端截短可能产生了v-kit的转化潜能。