Alternative miRNA biogenesis pathways and the interpretation of core miRNA pathway mutants

Mol Cell. 2011 Sep 16;43(6):892-903. doi: 10.1016/j.molcel.2011.07.024.

Abstract

Since the establishment of a canonical animal microRNA biogenesis pathway driven by the RNase III enzymes Drosha and Dicer, an unexpected variety of alternative mechanisms that generate functional microRNAs have emerged. We review here the many Drosha-independent and Dicer-independent microRNA biogenesis strategies characterized over the past few years. Beyond reflecting the flexibility of small RNA machineries, the existence of noncanonical pathways has consequences for interpreting mutants in the core microRNA machinery. Such mutants are commonly used to assess the consequences of "total" microRNA loss, and indeed, they exhibit many overall phenotypic similarities. Nevertheless, ongoing studies reveal a growing number of settings in which alternative microRNA pathways contribute to distinct phenotypes among core microRNA biogenesis mutants.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Argonaute Proteins
  • Drosophila / genetics
  • Drosophila / metabolism
  • Drosophila Proteins / genetics
  • Drosophila Proteins / physiology
  • Eukaryotic Initiation Factors / genetics
  • Eukaryotic Initiation Factors / physiology
  • Gene Expression Regulation / physiology
  • Humans
  • MicroRNAs / biosynthesis*
  • MicroRNAs / chemistry
  • Models, Genetic
  • Mutation*
  • Olfactory Pathways / metabolism
  • RNA Splicing
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins
  • RNA-Induced Silencing Complex / genetics
  • RNA-Induced Silencing Complex / physiology
  • Ribonuclease III / physiology

Substances

  • AGO1 protein, Drosophila
  • AGO2 protein, Drosophila
  • Argonaute Proteins
  • Drosophila Proteins
  • Eukaryotic Initiation Factors
  • MicroRNAs
  • RNA, Messenger
  • RNA-Binding Proteins
  • RNA-Induced Silencing Complex
  • Ribonuclease III