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The zinc finger-containing transcription factor Gata-4 is expressed in the developing endocrine pancreas and activates glucagon gene expression

机译:含锌指的转录因子Gata-4在发育中的内分泌胰腺中表达并激活胰高血糖素基因表达

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摘要

Gene inactivation studies have shown that members of the Gata family of transcription factors are critical for endoderm development throughout evolution. We show here that Gata-4 and/or Gata-6 are not only expressed in the adult exocrine pancreas but also in glucagonoma and insulinoma cell lines, whereas Gata-5 is restricted to the exocrine pancreas. During pancreas development, Gata-4 is expressed already at embryonic d 10.5 and colocalizes with early glucagon+ cells at embryonic d 12.5. Gata-4 was able to transactivate the glucagon gene both in heterologous BHK-21 (nonislet Syrian baby hamster kidney) and in glucagon-producing InR1G9 cells. Using gel-mobility shift assays, we identified a complex formed with nuclear extracts from InR1G9 cells on the G5 control element (-140 to -169) of the glucagon gene promoter as Gata-4. Mutation of the GATA binding site on G5 abrogated the transcriptional activation mediated by Gata-4 and reduced basal glucagon gene promoter activity in glucagon-producing cells by 55%. Furthermore, Gata-4 acted more than additively with Forkhead box A (hepatic nuclear factor-3) to trans-activate the glucagon gene promoter. We conclude that, besides its role in endoderm differentiation, Gata-4 might be implicated in the regulation of glucagon gene expression in the fetal pancreas and that Gata activity itself may be modulated by interactions with different cofactors.
机译:基因失活研究表明,转录因子Gata家族成员对于整个进化过程中的内胚层发育至关重要。我们在这里显示,Gata-4和/或Gata-6不仅在成年外分泌胰腺中表达,而且在胰高血糖素瘤和胰岛素瘤细胞系中表达,而Gata-5仅限于外分泌胰腺。在胰腺发育过程中,Gata-4已在胚胎d 10.5处表达,并与早期胰高血糖素+细胞在胚胎d 12.5共定位。 Gata-4能够在异源BHK-21(非胰岛叙利亚小仓鼠肾脏)和产生胰高血糖素的InR1G9细胞中激活胰高血糖素基因。使用凝胶迁移率移动分析,我们确定了与胰高血糖素基因启动子的G5控制元件(-140至-169)上的InR1G9细胞核提取物形成的复合物,即Gata-4。 G5上GATA结合位点的突变消除了Gata-4介导的转录激活,并使产生胰高血糖素的细胞中的基础胰高血糖素基因启动子活性降低了55%。此外,Gata-4与叉头盒A(肝核因子3)起着加和作用,从而反式激活胰高血糖素基因启动子。我们得出的结论是,除了其在内胚层分化中的作用外,Gata-4可能与胎儿胰腺胰高血糖素基因表达的调节有关,并且Gata活性本身可能受到与不同辅因子相互作用的调节。

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