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胰岛素瘤与成纤维体细胞杂种中人类胰岛素基因表达的缺失涉及顺式作用DNA元件。

Extinction of the human insulin gene expression in insulinoma x fibroblast somatic cell hybrids involves cis-acting DNA elements.

作者信息

Besnard C, Monthioux E, Loràs P, Jami J, Daegelen D

机构信息

Unité INSERM 257, Institut Jacques Monod du CNRS, Université Paris VII, France.

出版信息

J Cell Physiol. 1991 Mar;146(3):349-55. doi: 10.1002/jcp.1041460303.

Abstract

Insulin gene expression in rat insulinoma (RIN) cells is extinct in RIN x fibroblast hybrids and can reappear upon loss of DNA contributed by the fibroblast parent. (Besnard et al., Exp. Cell Res. 185:101-108, 1989). In the present study, we looked for the role of 5'-flanking sequences of the human insulin gene in the negative control observed in the hybrids. RIN cells were transformed with composite genes which consisted of the coding sequence of the gpt gene placed under the control of 5'-flanking regions of the human insulin gene (Ins.gpt gene). Upon hybridization of these cells with mouse fibroblasts, the expression of both Ins.gpt and endogenous rat insulin genes were suppressed together. The results obtained indicate that cis-acting DNA elements are involved in the negative control of the gene. These elements are located in a fragment spread from -258 to +241 of the transcription origin of the human insulin gene.

摘要

大鼠胰岛素瘤(RIN)细胞中的胰岛素基因表达在RIN与成纤维细胞的杂种细胞中消失,并且在成纤维细胞亲本贡献的DNA丢失后可能重新出现。(贝斯纳德等人,《实验细胞研究》185:101 - 108,1989年)。在本研究中,我们探究了人胰岛素基因5'侧翼序列在杂种细胞中观察到的负调控中的作用。用复合基因转化RIN细胞,这些复合基因由置于人胰岛素基因5'侧翼区域(Ins.gpt基因)控制下的gpt基因编码序列组成。当这些细胞与小鼠成纤维细胞杂交时,Ins.gpt基因和内源性大鼠胰岛素基因的表达同时受到抑制。所得结果表明顺式作用DNA元件参与了该基因的负调控。这些元件位于人胰岛素基因转录起始点从 - 258到 + 241的片段中。

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