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在小鼠成骨细胞(MC3T3-E1)中由促肿瘤的12-O-十四烷酰佛波醇-13-乙酸酯诱导产生且在ras转化细胞中组成性表达的基因序列的分离。

Isolation of a gene sequence induced later by tumor-promoting 12-O-tetradecanoylphorbol-13-acetate in mouse osteoblastic cells (MC3T3-E1) and expressed constitutively in ras-transformed cells.

作者信息

Nose K, Saito H, Kuroki T

机构信息

Department of Cancer Cell Research, University of Tokyo, Japan.

出版信息

Cell Growth Differ. 1990 Nov;1(11):511-8.

PMID:2088477
Abstract

Growth factors and tumor-promoting phorbol esters induce various types of "early response" genes, most of which encode transcription factors. To identify possible target genes for these early response gene products, we isolated complementary DNA clones of genes that were induced later by 12-O-tetradecanoylphorbol-13-acetate. A complementary DNA library was constructed using mRNA from mouse osteoblastic cells (MC3T3-E1) treated with 12-O-tetradecanoylphorbol-13-acetate for 4 h, and the library was screened by differential hybridization. Five independent clones were isolated. All of these genes were induced maximally 4 to 8 h after 12-O-tetradecanoylphorbol-13-acetate addition. Sequencing showed that three of them (OTS-1, -3, and -4) were those of the metallothionein II gene, and one (OTS-5) was identical to the osteopontin/2ar gene. The other (OTS-8) had no significant homology with known sequences and was considered to be a novel gene. The induction of OTS-5 and OTS-8 was decreased in the presence of cycloheximide. In mice, OTS-8 mRNA was detected in the lungs but not at appreciable levels in other organs. Open reading frame of OTS-8 complementary DNA and its in vitro transcription/translation product suggested that this gene encodes an Mr 26,000 protein. OTS-8 mRNA was induced by epidermal growth factor but not by serum. The steady-state levels of OTS-5 and OTS-8 mRNAs were significantly elevated in v-ras-transformed MC3T3 cells.

摘要

生长因子和促肿瘤佛波酯可诱导多种类型的“早期反应”基因,其中大多数编码转录因子。为了确定这些早期反应基因产物可能的靶基因,我们分离了由12-O-十四烷酰佛波醇-13-乙酸酯(TPA)随后诱导的基因的互补DNA克隆。使用经TPA处理4小时的小鼠成骨细胞(MC3T3-E1)的mRNA构建互补DNA文库,并通过差异杂交筛选该文库。分离出五个独立的克隆。所有这些基因在添加TPA后4至8小时达到最大诱导。测序表明其中三个(OTS-1、-3和-4)是金属硫蛋白II基因的克隆,一个(OTS-5)与骨桥蛋白/2ar基因相同。另一个(OTS-8)与已知序列无明显同源性,被认为是一个新基因。在放线菌酮存在下,OTS-5和OTS-8的诱导作用减弱。在小鼠中,OTS-8 mRNA在肺中可检测到,但在其他器官中含量不高。OTS-8互补DNA的开放阅读框及其体外转录/翻译产物表明该基因编码一种分子量为26,000的蛋白质。OTS-8 mRNA由表皮生长因子诱导,但不由血清诱导。在v-ras转化的MC3T3细胞中,OTS-5和OTS-8 mRNA的稳态水平显著升高。

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