Avnit-Sagi Tali, Vana Tal, Walker Michael D
Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.
Exp Diabetes Res. 2012;2012:891216. doi: 10.1155/2012/891216. Epub 2012 Jun 20.
MicroRNAs (miRNAs) are a class of small non-coding RNAs that play an important role in mediating a broad and expanding range of biological activities. miR-375 is expressed selectively in the pancreas. We have previously shown that selective expression of miR-375 in pancreatic beta cells is controlled by transcriptional mechanisms operating through a TATA box-containing promoter. Expression of miR-375 has been reported in non-beta cells within the endocrine pancreas, and indeed inactivation of miR-375 leads to perturbation in cell mass and number of both alpha and beta cells. Consistent with its expression throughout the endocrine pancreas, we now show that the promoter of the miR-375 gene shows selective activity in pancreatic endocrine alpha cells, comparable to that observed in beta cells. We previously identified a novel negative regulatory element located downstream of the miR-375 gene transcription start site. By generating luciferase reporter genes, we now show that the sequence is functional also when positioned upstream of a heterologous promoter, thus proving that the repressor effect is mediated at least in part at the level of transcription. Further characterization of the transcriptional control mechanism regulating expression of miR-375 and other pancreatic miRNAs will contribute to a better understanding of pancreas development and function.
微小RNA(miRNA)是一类小的非编码RNA,在介导广泛且不断扩展的生物活性中发挥重要作用。miR-375在胰腺中选择性表达。我们之前已经表明,miR-375在胰腺β细胞中的选择性表达受通过含TATA盒启动子起作用的转录机制控制。据报道,miR-375在内分泌胰腺的非β细胞中也有表达,实际上,miR-375的失活会导致α细胞和β细胞的细胞量和数量发生紊乱。与其在内分泌胰腺中的表达情况一致,我们现在表明,miR-375基因的启动子在胰腺内分泌α细胞中显示出选择性活性,与在β细胞中观察到的情况相当。我们之前在miR-375基因转录起始位点下游鉴定出一个新的负调控元件。通过生成荧光素酶报告基因,我们现在表明,当该序列位于异源启动子上游时也具有功能,从而证明这种抑制作用至少部分是在转录水平介导的。对调控miR-375和其他胰腺miRNA表达的转录控制机制进行进一步表征,将有助于更好地理解胰腺的发育和功能。