Hardon E M, Frain M, Paonessa G, Cortese R
European Molecular Biology Laboratory, Heidelberg, FRG.
EMBO J. 1988 Jun;7(6):1711-9. doi: 10.1002/j.1460-2075.1988.tb03000.x.
A segment of the human alpha 1-antitrypsin (alpha 1AT) 5'-flanking region comprising nucleotides -137 to -37 from the start of transcription is sufficient to drive liver-specific transcription from the homologous alpha 1AT promoter and from the heterologous SV40 promoter. In this paper we characterize two proteins, LF-A1 and LF-B1, whose ability to bind wild-type and mutant alpha 1AT promoter segments correlates with the ability of these segments to activate transcription in vivo. DNase I protection and methylation interference analysis reveals that LF-A1 recognizes sequences present in the regulatory region of the human alpha 1-antitrypsin, apolipoprotein A1 and haptoglobin-related genes. These sequences share a common 5' TGG/A A/C CC 3' motif. LF-B1 binds to the palindrome 5' TGGTTAAT/ATTCACCA 3' which is present in the human alpha 1-antitrypsin gene between positions -78 and -62 from the start of transcription. LF-B1 also recognizes a related sequence present in the human albumin gene between -66 and -50. These results suggest that LF-A1 and LF-B1 are common positive trans-acting factors which are required for the expression of several genes in the hepatocyte.
人α1 -抗胰蛋白酶(α1AT)5'侧翼区中从转录起始点起包含核苷酸-137至-37的片段,足以驱动来自同源α1AT启动子和异源SV40启动子的肝脏特异性转录。在本文中,我们鉴定了两种蛋白质,LF - A1和LF - B1,它们与野生型和突变型α1AT启动子片段结合的能力与这些片段在体内激活转录的能力相关。DNA酶I保护和甲基化干扰分析表明,LF - A1识别存在于人α1 -抗胰蛋白酶、载脂蛋白A1和触珠蛋白相关基因调控区域中的序列。这些序列共享一个共同的5'TGG/A A/C CC 3'基序。LF - B1结合于人α1 -抗胰蛋白酶基因中从转录起始点起-78至-62位之间存在的回文序列5'TGGTTAAT/ATTCACCA 3'。LF - B1还识别存在于人白蛋白基因中-66至-50位之间的一个相关序列。这些结果表明,LF - A1和LF - B1是肝细胞中几种基因表达所需的常见正向反式作用因子。