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c-Myb oncoprotein is an essential target of the dleu2 tumor suppressor microRNA cluster.

机译:c-Myb癌蛋白是dleu2抑癌微RNA簇的重要靶标。

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摘要

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 down-regulates 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.
机译:dleu2抑癌基因座编码两个microRNA,miR-15a和miR-16,被认为在B细胞肿瘤中起重要作用。然而,关于调控该微小RNA簇或受其调控的蛋白质的知之甚少。在这里,我们证明Pax5癌蛋白下调dleu2基因,并同时增强其自身异二聚体伴侣c-Myb的表达。有趣的是,c-Myb的上调主要发生在转录后水平,这表明它可能是miR-15a / 16等microRNA的靶标。实际上,miR-15a / 16已在c-Myb 3'-UTR中预测了结合位点,并通过它们减少了萤光素酶传感器测定中的蛋白质输出。此外,miR-15a / 16的强制过度表达降低了内源性c-Myb水平并损害了Pax5功能。相反,恢复c-Myb水平可部分缓解miR-15a / 16对肿瘤的抑制作用,这表明c-Myb是该microRNA簇的关键下游靶标。

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