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Pancreatic-Duodenal Homeobox 1 Regulates Expression of Liver Receptor Homolog 1 during Pancreas Development

机译:胰腺十二指肠同源盒1调节胰腺发育过程中肝受体同源1的表达。

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摘要

Liver receptor homolog 1 (LRH-1) and pancreatic-duodenal homeobox 1 (PDX-1) are coexpressed in the pancreas during mouse embryonic development. Analysis of the regulatory region of the human LRH-1 gene demonstrated the presence of three functional binding sites for PDX-1. Electrophoretic mobility shift assays and chromatin immunoprecipitation analysis showed that PDX-1 bound to the LRH-1 promoter, both in cultured cells in vitro and during pancreatic development in vivo. Retroviral expression of PDX-1 in pancreatic cells induced the transcription of LRH-1, whereas reduced PDX-1 levels by RNA interference attenuated its expression. Consistent with direct regulation of LRH-1 expression by PDX-1, PDX-1−/− mice expressed smaller amounts of LRH-1 mRNA in the embryonic pancreas. Taken together, our data indicate that PDX-1 controls LRH-1 expression and identify LRH-1 as a novel downstream target in the PDX-1 regulatory cascade governing pancreatic development, differentiation, and function.
机译:在小鼠胚胎发育过程中,肝脏受体同源物1(LRH-1)和胰十二指肠同源盒1(PDX-1)在胰腺中共表达。人LRH-1基因调控区的分析表明存在PDX-1的三个功能结合位点。电泳迁移率迁移分析和染色质免疫沉淀分析表明,PDX-1在体外培养细胞和体内胰腺发育过程中均与LRH-1启动子结合。 PDX-1在胰腺细胞中的逆转录病毒表达诱导了LRH-1的转录,而RNA干扰降低了PDX-1的水平则减弱了其表达。与PDX-1对LRH-1表达的直接调节一致,PDX-1-/-小鼠在胚胎胰腺中表达的LRH-1 mRNA含量更小。综上所述,我们的数据表明PDX-1控制LRH-1的表达并将LRH-1识别为PDX-1调控级联反应中胰腺发育,分化和功能的新型下游靶标。

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