Magenheim Judith, Hertz Rachel, Berman Ina, Nousbeck Janna, Bar-Tana Jacob
Department of Human Nutrition and Metabolism, Hebrew University Medical School, Jerusalem 91120, Israel.
Biochem J. 2005 May 15;388(Pt 1):325-32. doi: 10.1042/BJ20041802.
HNF-4alpha (hepatocyte nuclear factor-4alpha) is required for tissue-specific expression of many of the hepatic, pancreatic, enteric and renal traits. Heterozygous HNF-4alpha mutants are inflicted by MODY-1 (maturity onset diabetes of the young type-1). HNF-4alpha expression is reported here to be negatively autoregulated by HNF-4alpha1 and to be activated by dominant-negative HNF-4alpha1. Deletion and chromatin immunoprecipitation analysis indicated that negative autoregulation by HNF-4alpha1 was mediated by its association with the TATA-less HNF-4alpha core promoter enriched in Sp1, but lacking DR-1 response elements. Also, negative autoregulation by HNF-4alpha1 was independent of its transactivation function, being similarly exerted by transcriptional-defective MODY-1 missense mutants of HNF-4alpha1, or under conditions of suppressing or enhancing HNF-4alpha activity by small heterodimer partner or by inhibiting histone deacetylase respectively. Negative autoregulation by HNF-4alpha1 was abrogated by overexpressed Sp1. Transcriptional suppression by HNF-4alpha1 independently of its transactivation function may extend the scope of its transcriptional activity to interference with docking of the pre-transcriptional initiation complex to TATA-less promoters.
肝细胞核因子4α(HNF-4α)是许多肝脏、胰腺、肠道和肾脏特征性组织特异性表达所必需的。杂合型HNF-4α突变体受青少年发病的成年型糖尿病1型(MODY-1)影响。本文报道HNF-4α的表达受到HNF-4α1的负向自动调节,并被显性负性HNF-4α1激活。缺失和染色质免疫沉淀分析表明,HNF-4α1的负向自动调节是通过其与富含Sp1但缺乏DR-1反应元件的无TATA框的HNF-4α核心启动子的结合介导的。此外,HNF-4α1的负向自动调节与其反式激活功能无关,由HNF-4α1的转录缺陷型MODY-1错义突变体同样发挥作用,或分别在小异源二聚体伴侣抑制或增强HNF-4α活性的条件下,或通过抑制组蛋白脱乙酰酶发挥作用。过表达的Sp1可消除HNF-4α1的负向自动调节。HNF-4α1不依赖其反式激活功能的转录抑制可能会将其转录活性范围扩展至干扰转录前起始复合物与无TATA框启动子的对接。