Sp家族转录因子在JAR绒毛膜癌细胞中调控人层粘连蛋白α1基因

Tomoaki Niimi , Yoshitaka Hayashi , Kiyotoshi Sekiguchi , Yasuo Kitagawa
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引用次数: 10

摘要

层粘连蛋白-111 (α1β1γ1)是胚胎和胚外基底膜的主要成分。层粘连蛋白α1链在不同的上皮组织基底膜中表达受限,而β1和γ1链在组织中广泛分布。为了了解人层粘连蛋白α1链的表达是如何被控制的,我们克隆了人层粘连蛋白α1 (LAMA1)基因的5 ' -侧翼区域并对其进行了表征。用序列缺失启动子构建体和JAR绒绒膜癌细胞进行转染研究发现,最小的启动子片段位于+ 31至−206区域,该区域包含许多富含GC-和GT/ a的基序,用于结合Sp家族的转录因子。电泳迁移率和突变分析表明Sp1和Sp3特异性结合这些元件,对启动子活性很重要。此外,我们发现kr ppel样因子KLF4和KLF6也能激活人LAMA1基因的转录。染色质免疫沉淀分析显示这些转录因子募集到启动子区域。这些结果表明,人LAMA1基因的转录受Sp1/Sp3和kr ppel样因子、KLF4和KLF6的共同作用控制。
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The Sp family of transcription factors regulates the human laminin α1 gene in JAR choriocarcinoma cells

Laminin-111 (α1β1γ1) is the major component of the embryonic and extra-embryonic basement membrane. The laminin α1 chain shows a restricted and developmentally regulated expression in basement membranes of distinct epithelial tissues while β1 and γ1 chains have a wide tissue distribution. To understand how human laminin α1 chain expression is controlled, we cloned and characterized the 5′-flanking region of the human laminin α1 (LAMA1) gene. Transfection studies using serially deleted promoter constructs and JAR choriocarcinoma cells revealed that the minimal promoter fragment resided in the + 31 to − 206 region, which contains a number of GC- and GT/A-rich motifs for the binding of the Sp family of transcription factors. Electrophoretic mobility shift assays and mutational analyses revealed that Sp1 and Sp3 bound specifically to these elements and are important for the promoter activity. Furthermore, we showed that Krüppel-like factors KLF4 and KLF6 also activate transcription of the human LAMA1 gene. Chromatin immunoprecipitation analysis demonstrated recruitment of these transcription factors to the promoter region. These results indicate that transcription of the human LAMA1 gene is controlled by a combination of the actions of Sp1/Sp3 and Krüppel-like factors, KLF4 and KLF6.

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