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

被引:55
作者
Watada, H
Mirmira, RG
Leung, J
German, MS
机构
[1] Univ Calif San Francisco, Hormone Res Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
关键词
D O I
10.1074/jbc.M004981200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:34224 / 34230
页数:7
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