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脂肪生成细胞系1246中一种与分化相关的信使核糖核酸的分子克隆

Molecular cloning of a differentiation-related mRNA in the adipogenic cell line 1246.

作者信息

Jiang H P, Harris S E, Serrero G

机构信息

W. Alton Jones Cell Science Center, Inc., Lake Placid, New York 12946-1099.

出版信息

Cell Growth Differ. 1992 Jan;3(1):21-30.

PMID:1376140
Abstract

The 1246 cell line is a C3H mouse teratoma-derived adipogenic cell line that can proliferate and differentiate in defined medium. We have constructed a recombinant phage library containing complementary DNAs (cDNAs) prepared from mRNA of differentiated 1246 cells. This library was screened using a differential hybridization technique. We have isolated five different cDNA clones corresponding to mRNAs that are induced during adipogenesis of 1246 cells and one cDNA clone corresponding to mRNA that is decreased during adipogenesis. Among the mRNAs expressed during adipose differentiation, some are not expressed in undifferentiated cells, whereas some are expressed at very low levels under these conditions. Moreover, the level of induction during differentiation and the temporal expression of the mRNAs corresponding to these cDNAs varied. Our results indicate that one of the cDNA clones isolated, called 154, which selects a 2.2-kilobase mRNA, was induced 100-fold at a very early time during the onset of the differentiation program in 1246 cells and also in adipocyte precursors in primary culture. Direct sequencing of 154 cDNA insert revealed no homology with sequences in GenBank and PIR protein databases. The expression of 154 mRNA was stimulated by accelerators of differentiation such as dexamethasone and isobutylmethylxanthine and inhibited by tumor necrosis factor alpha, transforming growth factor beta, and epidermal growth factor, which are known inhibitors of 1246 cell differentiation. In addition, 154 mRNA level in adipocytes was down-regulated by tumor necrosis factor alpha, but not by transforming growth factor beta or epidermal growth factor. These results suggest that the increase in 154 mRNA expression is related to the onset of adipose differentiation. Further analysis of this clone should allow characterization of a novel protein induced early during the process of differentiation.

摘要

1246细胞系是一种源自C3H小鼠畸胎瘤的脂肪生成细胞系,可在限定培养基中增殖和分化。我们构建了一个重组噬菌体文库,其中包含从分化的1246细胞的mRNA制备的互补DNA(cDNA)。使用差异杂交技术对该文库进行筛选。我们分离出了五个与1246细胞脂肪生成过程中诱导产生的mRNA相对应的不同cDNA克隆,以及一个与脂肪生成过程中表达量降低的mRNA相对应的cDNA克隆。在脂肪分化过程中表达的mRNA中,有些在未分化细胞中不表达,而有些在这些条件下表达水平极低。此外,分化过程中的诱导水平以及与这些cDNA相对应的mRNA的时间表达各不相同。我们的结果表明,分离出的一个名为154的cDNA克隆,它选择了一个2.2千碱基的mRNA,在1246细胞以及原代培养的脂肪细胞前体的分化程序开始的非常早期就被诱导了100倍。对154 cDNA插入片段的直接测序显示与GenBank和PIR蛋白质数据库中的序列没有同源性。154 mRNA的表达受到地塞米松和异丁基甲基黄嘌呤等分化促进剂的刺激,并受到肿瘤坏死因子α、转化生长因子β和表皮生长因子的抑制,这些都是已知的1246细胞分化抑制剂。此外,脂肪细胞中154 mRNA的水平被肿瘤坏死因子α下调,但不受转化生长因子β或表皮生长因子的影响。这些结果表明154 mRNA表达的增加与脂肪分化的开始有关。对该克隆的进一步分析应该能够鉴定出在分化过程早期诱导产生的一种新蛋白质的特征。

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