Wang M, Drucker D J
Banting and Best Diabetes Centre, Toronto Hospital, University of Toronto, Canada.
J Biol Chem. 1995 May 26;270(21):12646-52. doi: 10.1074/jbc.270.21.12646.
The LIM domain homeobox gene islet 1 (isl-1) is expressed in the embryonic nervous system and may be an early marker of motor neuron specification. isl-1 is expressed in all 4 islet cell types, but a role for isl-1 in the regulation of insulin gene expression has not been demonstrated, and the genetic targets for isl-1 in the pancreas remain unknown. We show here that the proximal rat proglucagon gene promoter binds an amino-terminally truncated Trp-E-isl-1 fusion protein that lacks the LIM domains. The proglucagon gene promoter also binds full-length in vitro translated isl-1 containing the intact LIM domains. isl-1 antisera detects binding of proglucagon gene sequences to isl-1 present in a slowly-migrating complex in nuclear extracts from InR1-G9 islet cells. The transcriptional properties of the proglucagon gene promoter sequences that bind isl-1 (designated Ga, Gb, and Gc) were assessed after transfection of reporter genes into wild type and isl-1-antisense (isl-1(AS)) InR1-G9 islet cells. The proximal proglucagon gene (Ga) promoter sequence reduced TK-CAT activity by approximately 50%, but no change in the activity of the Ga-TK-CAT plasmid was seen after transfection of isl-1(AS) InR1-G9 cells. In contrast, the Gb/Gc sites activated transcription 2-3 fold in wild type InR1-G9 cells, and the isl-1-dependent activation of gene transcription through the Gb/Gc element was eliminated following transfection of isl-1(AS) InR1-G9 cells. These data demonstrate that the LIM domain homeobox gene isl-1 1) is not constrained from DNA binding by its LIM domains and 2) functions as a positive regulator of proglucagon gene transcription in the endocrine pancreas.
LIM结构域同源框基因胰岛1(isl-1)在胚胎神经系统中表达,可能是运动神经元特化的早期标志物。isl-1在所有4种胰岛细胞类型中均有表达,但isl-1在胰岛素基因表达调控中的作用尚未得到证实,其在胰腺中的基因靶点仍不清楚。我们在此表明,大鼠胰高血糖素原基因近端启动子可结合一种氨基末端截短的、缺乏LIM结构域的Trp-E-isl-1融合蛋白。胰高血糖素原基因启动子也能结合含有完整LIM结构域的全长体外翻译的isl-1。isl-1抗血清可检测到胰高血糖素原基因序列与InR1-G9胰岛细胞核提取物中一个迁移缓慢的复合物中的isl-1的结合。在将报告基因转染到野生型和isl-1反义(isl-1(AS))InR1-G9胰岛细胞后,评估了与isl-1结合的胰高血糖素原基因启动子序列(命名为Ga、Gb和Gc)的转录特性。胰高血糖素原基因近端(Ga)启动子序列使TK-CAT活性降低约50%,但在转染isl-1(AS) InR1-G9细胞后,Ga-TK-CAT质粒的活性未见变化。相反,Gb/Gc位点在野生型InR1-G9细胞中使转录激活2 - 3倍,在转染isl-1(AS) InR1-G9细胞后,通过Gb/Gc元件的isl-1依赖性基因转录激活被消除。这些数据表明,LIM结构域同源框基因isl-1:1)其LIM结构域并不限制其与DNA的结合;2)在内分泌胰腺中作为胰高血糖素原基因转录的正调控因子发挥作用。