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. 2014 Sep 1;2014:920134. doi: 10.1155/2014/920134

Figure 1.

Figure 1

Biogenesis of miRNA. miRNAs are transcribed from DNA into primary-miRNAs (Pri-miRNAs) which contain hairpin-like structures. RNase III Drosha and its binding partner, DiGeorge syndrome critical region gene 8 (DGCR8), bind to the hairpin structures in Pri-miRNAs and process them into precursor miRNAs (Pre-miRNAs). Through Exportin 5, Pre-miRNAs are transferred into cytoplasm and are processed by another RNase III enzyme, Dicer, in collaboration with transactivating response RNA-binding protein (TRBP) to generate the mature miRNA duplex. One strand of the duplex goes into RNA-induced silencing complex (RISC), while the other is degraded. In RISC, mature miRNA recognizes target mRNAs through sequence complementarity, resulting in either degradation of the target mRNA (perfect complementarity to 3′UTR) or more frequently inhibition of translation (imperfect complementarity to 3′UTR).