Department of Pathobiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Cancer Biol Ther. 2008 Nov;7(11):1758-64. doi: 10.4161/cbt.7.11.6722. Epub 2008 Nov 4.
The dleu2 tumor suppressor locus encodes two microRNAs, miR-15a and miR-16, which are thought to play an important role in B-cell neoplasms. However, relatively little is known about proteins that regulate or are regulated by this microRNA cluster. Here we demonstrate that the Pax5 oncoprotein downregulates the dleu2 gene and at the same time boosts expression of its own heterodimeric partner c-Myb. Interestingly, c-Myb upregulation occurs primarily at a post-transcriptional level, suggesting that it might be a target for microRNAs such as miR-15a/16. Indeed, miR-15a/16 have predicted binding sites in the c-Myb 3'-UTR and through them diminish protein output in luciferase sensor assays. Moreover, forced overexpression of miR-15a/16 reduces endogenous c-Myb levels and compromises Pax5 function. Conversely, restoration of c-Myb levels partly alleviates tumors suppressive effects of miR-15a/16, suggesting that c-Myb is a key downstream target of this microRNA cluster.
Dleu2 肿瘤抑制基因座编码两个 microRNA,miR-15a 和 miR-16,它们被认为在 B 细胞肿瘤中发挥重要作用。然而,关于调控该 microRNA 簇的蛋白或受其调控的蛋白知之甚少。在这里,我们证明 Pax5 癌蛋白下调 dleu2 基因,同时增强其异二聚体伙伴 c-Myb 的表达。有趣的是,c-Myb 的上调主要发生在转录后水平,表明它可能是 microRNA 如 miR-15a/16 的靶标。事实上,miR-15a/16 在 c-Myb 3'-UTR 上有预测的结合位点,并通过它们在荧光素酶传感器测定中减少蛋白质输出。此外,miR-15a/16 的强制过表达降低内源性 c-Myb 水平并损害 Pax5 功能。相反,c-Myb 水平的恢复部分缓解了 miR-15a/16 的肿瘤抑制作用,表明 c-Myb 是该 microRNA 簇的关键下游靶标。