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- W56611421 abstract "Abstract MicroRNAs (miRNAs) are small noncoding RNAs that function as major players of posttranscriptional gene regulation in diverse species. In mammals, the biogenesis of miRNAs is executed by cooperation of multiple biochemical reactions including processing of miRNA precursors by two central endoribonucleases, Drosha and Dicer. While the transcription of miRNA precursors is regulated by various transcription factors, it has been recently unlabeled that miRNA maturation is further subjected to a range of regulatory mechanisms in miRNA processome. We previously demonstrated that a key regulator of tumor suppression, p53, modulates Drosha-mediated processing of primary miRNA transcripts. The pathways for miRNA maturation also dynamically cross talk with other intracellular signaling pathways. Further, we recently revealed that MCPIP1, an immune regulator, antagonizes Dicer and suppresses miRNA processing as another important endoribonuclease. In addition, recent evidences highlighted alterations of miRNA biogenesis in cancer pathogenesis. These advances in miRNA metabolome would bring deep insights for understanding alterations of miRNAs in diverse disease pathogenesis and for development of miRNA-based therapeutic applications. In this chapter, we summarize our findings and advances in miRNA metabology." @default.
- W56611421 created "2016-06-24" @default.
- W56611421 creator A5051009186 @default.
- W56611421 creator A5052170454 @default.
- W56611421 date "2012-01-01" @default.
- W56611421 modified "2023-10-18" @default.
- W56611421 title "Control of MicroRNA Maturation by p53 Tumor Suppressor and MCPIP1 Ribonuclease" @default.
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