Watada H, Kajimoto Y, Kaneto H, Matsuoka T, Fujitani Y, Miyazaki J i, Yamasaki Y
First Department of Medicine, Osaka University School of Medicine, Suita, 565, Japan.
Biochem Biophys Res Commun. 1996 Dec 24;229(3):746-51. doi: 10.1006/bbrc.1996.1875.
The AT-rich cis-motif A elements of the insulin gene promoter contribute to directing the gene's expression to pancreatic beta-cells, bound by a homeodomain-containing transcription factor, PDX-1/IPF1/STF-1/IDX-1. The islet amyloid polypeptide (IAPP; amylin) gene, which is also expressed in limited tissues such as pancreatic beta- and delta-cells, contained similar AT-rich sequences in its regulatory sequences. To understand the molecular basis of IAPP gene regulation, we evaluated the possible physiological significance of the motif in human IAPP gene regulation. All of the three typical A element-like sequences that matched the CT-box consensus (AT-1, -207/-202; AT-2, -154/-142; and AT-3, -88/-83) were shown to bind specifically to a nuclear factor in the beta-cell-derived MIN6 cells, which was subsequently identified immunologically as the insulin gene transcription factor PDX-1. When the promoter activity was examined in MIN6 cells, the disruption of AT-1 or AT-3 but not of AT-2 caused a marked reduction in the IAPP gene promoter. Thus, despite the observation that all the three A element-like regions could bind to PDX-1, the AT-2 site may not be involved in mediating the PDX-1 action in vivo. These observations suggest the involvement of PDX-1 in human IAPP gene regulation, which seems to be mediated through at least two A element-like cis-motifs in the gene promoter.
胰岛素基因启动子富含AT的顺式基序A元件有助于将该基因的表达导向胰岛β细胞,它由一种含同源结构域的转录因子PDX-1/IPF1/STF-1/IDX-1结合。胰岛淀粉样多肽(IAPP;胰淀素)基因也在诸如胰岛β细胞和δ细胞等有限的组织中表达,其调控序列中含有类似的富含AT的序列。为了理解IAPP基因调控的分子基础,我们评估了该基序在人类IAPP基因调控中的可能生理意义。所有与CT盒共有序列匹配的三个典型A元件样序列(AT-1,-207/-202;AT-2,-154/-142;以及AT-3,-88/-83)均显示在β细胞来源的MIN6细胞中特异性结合一种核因子,随后通过免疫鉴定该核因子为胰岛素基因转录因子PDX-1。当在MIN6细胞中检测启动子活性时,AT-1或AT-3的破坏而非AT-2的破坏导致IAPP基因启动子显著降低。因此,尽管观察到所有三个A元件样区域均可与PDX-1结合,但AT-2位点可能不参与介导体内的PDX-1作用。这些观察结果表明PDX-1参与人类IAPP基因调控,这似乎是通过基因启动子中至少两个A元件样顺式基序介导的。