Rastegar M, Szpirer C, Rousseau G G, Lemaigre F P
Hormone and Metabolic Research Unit, Louvain University Medical School and Christian de Duve Institute of Cellular Pathology (ICP), Avenue Hippocrate 75, B-1200 Brussels, Belgium.
Biochem J. 1998 Sep 15;334 ( Pt 3)(Pt 3):565-9. doi: 10.1042/bj3340565.
Hepatocyte nuclear factor 6 (HNF-6) is the prototype of a family of tissue-specific transcription factors characterized by a bipartite DNA-binding domain consisting of a single cut domain and a novel type of homeodomain. We have previously cloned rat cDNA species coding for two isoforms, HNF-6alpha (465 residues) and beta (491 residues), which differ only by the length of the spacer between the two DNA-binding domains. We have now localized the rat Hnf6 gene to chromosome 8q24-q31 by Southern blotting of DNA from somatic cell hybrids and by fluorescence in situ hybridization. Cloning and sequencing of the rat gene showed that the two HNF-6 isoforms are generated by alternative splicing of three exons that are more than 10 kb apart from each other. Exon 1 codes for the N-terminal part and the cut domain, exon 2 codes for the 26 HNF-6beta-specific amino acids, and exon 3 codes for the homeodomain and the C-terminal amino acids. The transcription initiation site was mapped by ribonuclease protection and 5' rapid amplification of cDNA ends. Transfection experiments showed that promoter activity was contained within 0.75 kb upstream of the transcription initiation site. This activity was detected by the transfection of liver-derived HepG2 cells, but not of Rat-1 fibroblasts, suggesting that the promoter is sufficient to confer liver-specific expression.
肝细胞核因子6(HNF-6)是一类组织特异性转录因子家族的原型,其特征在于由单个切割结构域和新型同源结构域组成的双组分DNA结合结构域。我们之前克隆了编码两种异构体HNF-6α(465个残基)和β(491个残基)的大鼠cDNA物种,它们仅在两个DNA结合结构域之间的间隔区长度上有所不同。我们现在通过对体细胞杂种DNA的Southern印迹分析和荧光原位杂交,将大鼠Hnf6基因定位到染色体8q24-q31。大鼠基因的克隆和测序表明,两种HNF-6异构体是由彼此相距超过10 kb的三个外显子的可变剪接产生的。外显子1编码N端部分和切割结构域,外显子2编码26个HNF-6β特异性氨基酸,外显子3编码同源结构域和C端氨基酸。通过核糖核酸酶保护和cDNA末端的5'快速扩增来定位转录起始位点。转染实验表明,启动子活性存在于转录起始位点上游0.75 kb范围内。通过转染肝源性HepG2细胞而非Rat-1成纤维细胞检测到了这种活性,这表明该启动子足以赋予肝脏特异性表达。