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©The Author(s) 2015.
World J Gastroenterol. Sep 14, 2015; 21(34): 9853-9862
Published online Sep 14, 2015. doi: 10.3748/wjg.v21.i34.9853
Published online Sep 14, 2015. doi: 10.3748/wjg.v21.i34.9853
Figure 1 MicroRNAs biogenesis and function.
In the nucleus, pri-miRNAs are transcribed by RNA Polymerase II (Pol II) to pre-miRNAs after processing by the microprocessor complex, which consists of Drosha and DGCR8. Pre-miRNAs are exported from the nucleus to the cytoplasm by exportin-5 and processed into the miRNA-miRNA* duplex by Dicer. The duplex is separated into two strands: one strand is selected as the mature miRNA, and the other strand is degraded. Mature miRNAs are incorporated into RISC (RNA-induced silencing complex) to produce target mRNA repression (imperfect complementarity) or mRNA cleavage (perfect complementarity). pri-miRNAs: Primary miRNAs; Pol II: RNA Polymerase II; pre-miRNAs: MiRNAs precursor; DGCR8: DiGeorge syndrome critical region gene; miRNA: MicroRNA; RISC: RNA-induced silencing complex.
- Citation: Zhang YC, Xu Z, Zhang TF, Wang YL. Circulating microRNAs as diagnostic and prognostic tools for hepatocellular carcinoma. World J Gastroenterol 2015; 21(34): 9853-9862
- URL: https://www.wjgnet.com/1007-9327/full/v21/i34/9853.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i34.9853