Clevidence D E, Overdier D G, Peterson R S, Porcella A, Ye H, Paulson K E, Costa R H
Department of Biochemistry (M/C 536), College of Medicine, University of Illinois at Chicago 60612-7334.
Dev Biol. 1994 Nov;166(1):195-209. doi: 10.1006/dbio.1994.1307.
The hepatocyte nuclear factor-3 (HNF-3)/forkhead (fkh) proteins consist of an extensive family of tissue-specific and developmental gene regulators which share homology within the winged helix DNA binding motif. We report on the isolation of a new family member, HNF-3/forkhead homolog 8 (HFH-8), from lung cDNA libraries and the derivation of the complete amino acid sequences for the HFH-8 protein as well as previously identified HFH-1 and HFH-4 proteins. The HFH proteins contain several sequence motifs found in activation domains of other transcription factors and HNF-3/fkh family members. In situ hybridization with the HNF-3, HFH-4, and HFH-8 probes in adult lung demonstrate that the HNF-3/fkh cellular expression patterns are regionally specified. Whereas HNF-3 alpha and HNF-3 beta are normally coexpressed in the hepatocyte, their expression patterns in the lung are different. The HNF-3 alpha and HFH-4 genes are coexpressed in the bronchiolar epithelium (clara cells), whereas the HNF-3 beta probe exhibits prominent hybridization with the smooth muscle surrounding arterioles and bronchioles. In contrast, HFH-8 probes labeled the type II pneumocyte cells lining the respiratory surfaces of terminal bronchioles and alveolar sac. We have identified an HNF-3 consensus DNA binding sequence in the proximal surfactant protein B (SPB) promoter region (SPB-f2, -78 to -88). SPB gene transcription is restricted to bronchiolar and alveolar epithelium which colocalizes with the expression pattern of the HNF-3 alpha and HFH-8 genes, respectively. We show that the SPB-f2 sequence is recognized by both HNF-3 alpha and HFH-8 proteins and that these cDNA expression vectors activate the SPB promoter in cotransfection assays through the HNF-3 consensus sequence. Our results suggest that SPB promoter activity is regulated by HNF-3 alpha and HFH-8 proteins in a cell type-specific manner.
肝细胞核因子-3(HNF-3)/叉头(fkh)蛋白构成了一个庞大的组织特异性和发育基因调节因子家族,它们在翼状螺旋DNA结合基序内具有同源性。我们报告了从肺cDNA文库中分离出一个新的家族成员,即HNF-3/叉头同源物8(HFH-8),以及推导得到HFH-8蛋白以及先前鉴定的HFH-1和HFH-4蛋白的完整氨基酸序列。HFH蛋白含有在其他转录因子和HNF-3/fkh家族成员的激活域中发现的几个序列基序。用HNF-3、HFH-4和HFH-8探针在成年肺中进行原位杂交表明,HNF-3/fkh细胞表达模式是区域特异性的。虽然HNF-3α和HNF-3β通常在肝细胞中共表达,但它们在肺中的表达模式不同。HNF-3α和HFH-4基因在细支气管上皮(克拉拉细胞)中共表达,而HNF-3β探针与小动脉和细支气管周围的平滑肌有明显杂交信号。相比之下,HFH-8探针标记了终末细支气管和肺泡囊呼吸表面的II型肺上皮细胞。我们在表面活性蛋白B(SPB)启动子近端区域(SPB-f2,-78至-88)鉴定出一个HNF-3共有DNA结合序列。SPB基因转录仅限于细支气管和肺泡上皮,分别与HNF-3α和HFH-8基因的表达模式共定位。我们表明,SPB-f2序列可被HNF-3α和HFH-8蛋白识别,并且这些cDNA表达载体在共转染实验中通过HNF-3共有序列激活SPB启动子。我们的结果表明,SPB启动子活性以细胞类型特异性方式受HNF-3α和HFH-8蛋白调节。