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β细胞分化因子Nkx6.1的转录和翻译调控

Transcriptional and translational regulation of beta-cell differentiation factor Nkx6.1.

作者信息

Watada H, Mirmira R G, Leung J, German M S

机构信息

Hormone Research Institute, University of California, San Francisco, California 94143-0534, USA.

出版信息

J Biol Chem. 2000 Nov 3;275(44):34224-30. doi: 10.1074/jbc.M004981200.

DOI:10.1074/jbc.M004981200
PMID:10938085
Abstract

In the mature pancreas, the homeodomain transcription factor Nkx6.1 is uniquely restricted to beta-cells. Nkx6.1 also is expressed in developing beta-cells and plays an essential role in their differentiation. Among cell lines, both beta- and alpha-cell lines express nkx6.1 mRNA; but no protein can be detected in the alpha-cell lines, suggesting that post-transcriptional regulation contributes to the restriction of Nkx6.1 to beta-cells. To investigate the regulator of Nkx6.1 expression, we outlined the structure of the mouse nkx6.1 gene, and we identified regions that direct cell type-specific expression. The nkx6.1 gene has a long 5'-untranslated region (5'-UTR) downstream of a cluster of transcription start sites. nkx6.1 gene sequences from -5.6 to +1.0 kilobase pairs have specific promoter activity in beta-cell lines but not in NIH3T3 cells. This activity is dependent on sequences located at about -800 base pairs and on the 5'-UTR. Electrophoretic mobility shift assays demonstrate that homeodomain transcription factors PDX1 and Nkx2.2 can bind to the sequence element located at -800 base pairs. In addition, dicistronic assays establish that the 5'-UTR region functions as a potent internal ribosomal entry site, providing cell type-specific regulation of translation. These data demonstrate that complex regulation of both Nkx6.1 transcription and translation provides the specificity of expression required during pancreas development.

摘要

在成熟胰腺中,同源结构域转录因子Nkx6.1仅在β细胞中表达。Nkx6.1也在发育中的β细胞中表达,并在其分化过程中发挥重要作用。在细胞系中,β细胞系和α细胞系均表达nkx6.1 mRNA;但在α细胞系中未检测到蛋白质,这表明转录后调控导致Nkx6.1仅在β细胞中表达。为了研究Nkx6.1表达的调节因子,我们概述了小鼠nkx6.1基因的结构,并确定了指导细胞类型特异性表达的区域。nkx6.1基因在转录起始位点簇下游有一个长的5'非翻译区(5'-UTR)。从-5.6到+1.0千碱基对的nkx6.1基因序列在β细胞系中具有特异性启动子活性,但在NIH3T3细胞中没有。这种活性依赖于位于约-800碱基对处的序列和5'-UTR。电泳迁移率变动分析表明,同源结构域转录因子PDX1和Nkx2.2可以结合位于-800碱基对处的序列元件。此外,双顺反子分析表明,5'-UTR区域作为一个有效的内部核糖体进入位点,提供细胞类型特异性的翻译调控。这些数据表明,Nkx6.1转录和翻译的复杂调控为胰腺发育过程中所需的表达特异性提供了保障。

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