Degen S J, Stuart L A, Han S, Jamison C S
Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, Ohio.
Biochemistry. 1991 Oct 8;30(40):9781-91. doi: 10.1021/bi00104a030.
The cDNA and gene coding for mouse hepatocyte growth factor-like protein (HGF-like protein) were isolated and characterized. The size of the gene from the site of initiation of transcription to the polyadenylation site is 4613 bp in length and is composed of 18 exons separated by 17 intervening sequences. The exons range in size from 36 to 227 bp in length, while the intervening sequences range in size from 78 to 613 bp in length. The site of initiation of transcription was identified by primer extension analysis using total RNA isolated from mouse liver. On the basis of these results, the first exon is 146 bp in length and includes 94 bp of 5'-noncoding sequence. The sequence 5'TATGTG3' is present between 34 and 39 bp upstream of the transcription start site and could potentially be the TATA sequence found for many constitutively expressed eukaryotic genes to be the promoter for RNA polymerase II. The sequence 5'GCAAT3' at -96 to -92 may be the CCAAT sequence responsible for stimulation of transcription of some eukaryotic genes. The same sequences in the Genbank and NBRF databases were homologous to similar regions in the genes coding for both human and mouse HGF-like protein (Han et al., 1991). The acyl-peptide hydrolase gene is 410 bp downstream of the mouse HGF-like protein, but is transcribed from the complementary strand. The mouse cDNA for HGF-like protein codes for a putative protein with the same domain structure as its human homologue with four kringle domains followed by a serine protease-like domain. On the basis of the translated sequence of the cDNA, the mouse HGF-like protein would be 716 amino acids in length with a molecular weight of 80K. There are four potential N-linked carbohydrate attachment sites. The DNA and amino acid sequences of mouse HGF-like protein are compared to the human protein. Overall, the two proteins are about 80% identical with each other. In contrast to mRNA for human HGF-like protein, which is 2.4 and 3.0 kilobases in length in human liver, only the smaller species is seen in mouse and rat liver. The expression pattern of mRNA coding for HGF-like protein during development and in maternal rats was determined by Northern analysis. It is apparent that the majority of mRNA coding for HGF-like protein is expressed in liver. Messenger RNA is also expressed at a lower level in lung, adrenal, and placenta.
分离并鉴定了编码小鼠肝细胞生长因子样蛋白(HGF样蛋白)的cDNA和基因。从转录起始位点到聚腺苷酸化位点的基因长度为4613 bp,由18个外显子组成,被17个间隔序列隔开。外显子长度在36至227 bp之间,而间隔序列长度在78至613 bp之间。通过使用从小鼠肝脏分离的总RNA进行引物延伸分析来确定转录起始位点。基于这些结果,第一个外显子长度为146 bp,包括94 bp的5'-非编码序列。序列5'TATGTG3'存在于转录起始位点上游34至39 bp之间,可能是许多组成型表达的真核基因中发现的TATA序列,作为RNA聚合酶II的启动子。-96至-92处的序列5'GCAAT3'可能是负责刺激某些真核基因转录的CCAAT序列。Genbank和NBRF数据库中的相同序列与编码人和小鼠HGF样蛋白的基因中的相似区域同源(Han等人,1991)。酰基肽水解酶基因在小鼠HGF样蛋白下游410 bp处,但从互补链转录。小鼠HGF样蛋白的cDNA编码一种推定的蛋白质,其结构域结构与其人类同源物相同,具有四个kringle结构域,后面跟着一个丝氨酸蛋白酶样结构域。根据cDNA的翻译序列,小鼠HGF样蛋白长度为716个氨基酸,分子量为80K。有四个潜在的N-连接糖基化附着位点。将小鼠HGF样蛋白的DNA和氨基酸序列与人蛋白进行比较。总体而言,这两种蛋白彼此约80%相同。与人类肝脏中长度为2.4和3.0千碱基的人类HGF样蛋白mRNA不同,在小鼠和大鼠肝脏中仅观察到较小的物种。通过Northern分析确定了发育过程中和母鼠中编码HGF样蛋白的mRNA的表达模式。显然,大多数编码HGF样蛋白的mRNA在肝脏中表达。信使RNA在肺、肾上腺和胎盘中也以较低水平表达。