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小鼠met原癌基因的结构、组织特异性表达及转化活性

Structure, tissue-specific expression, and transforming activity of the mouse met protooncogene.

作者信息

Iyer A, Kmiecik T E, Park M, Daar I, Blair D, Dunn K J, Sutrave P, Ihle J N, Bodescot M, Vande Woude G F

机构信息

Rush Presbyterian St. Luke's Medical Center, Medical Oncology Department, Chicago, Illinois 60612.

出版信息

Cell Growth Differ. 1990 Feb;1(2):87-95.

PMID:2085463
Abstract

A 6.7-kilobase met complementary DNA (cDNA) was isolated from a pcD cDNA library prepared from C3H mouse fibroblast cell line polyadenylated RNA. Sequence analysis of 6.7-kilobase met cDNA insert revealed that it contained the entire open reading frame and shared an overall homology of 88.1% with the human met gene. Using the mouse met cDNA as probe, high levels of met expression were observed in the kidney, brain, lung, skin, and embryonic tissue as well as in several factor responsive mouse myeloid cell lines. Under SV40 promoter control, the mouse met protooncogene cDNA in the pCD vector was able to transform NIH 3T3 cells. These transformed cells possess multiple copies of mouse met cDNA and exhibit properties of malignant cells, including growth in soft agar and induction of tumors in nude mice. Tumor explant cell lines analyzed by Western blot also reveal the presence of high levels of Mr 170,000 and 140,000 met protein product(s).

摘要

从由C3H小鼠成纤维细胞系多聚腺苷酸化RNA制备的pcD cDNA文库中分离出一个6.7千碱基的met互补DNA(cDNA)。对6.7千碱基的met cDNA插入片段进行序列分析表明,它包含完整的开放阅读框,并且与人类met基因的总体同源性为88.1%。以小鼠met cDNA为探针,在肾脏、大脑、肺、皮肤和胚胎组织以及几种因子反应性小鼠髓样细胞系中观察到高水平的met表达。在SV40启动子控制下,pCD载体中的小鼠met原癌基因cDNA能够转化NIH 3T3细胞。这些转化细胞拥有多个小鼠met cDNA拷贝,并表现出恶性细胞的特性,包括在软琼脂中生长和在裸鼠中诱导肿瘤。通过蛋白质印迹分析的肿瘤外植体细胞系也显示存在高水平的分子量为170,000和140,000的met蛋白产物。

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