A splicing-independent function of SF2/ASF in microRNA processing

Mol Cell. 2010 Apr 9;38(1):67-77. doi: 10.1016/j.molcel.2010.02.021.

Abstract

Both splicing factors and microRNAs are important regulatory molecules that play key roles in posttranscriptional gene regulation. By miRNA deep sequencing, we identified 40 miRNAs that are differentially expressed upon ectopic overexpression of the splicing factor SF2/ASF. Here we show that SF2/ASF and one of its upregulated microRNAs (miR-7) can form a negative feedback loop: SF2/ASF promotes miR-7 maturation, and mature miR-7 in turn targets the 3'UTR of SF2/ASF to repress its translation. Enhanced microRNA expression is mediated by direct interaction between SF2/ASF and the primary miR-7 transcript to facilitate Drosha cleavage and is independent of SF2/ASF's function in splicing. Other miRNAs, including miR-221 and miR-222, may also be regulated by SF2/ASF through a similar mechanism. These results underscore a function of SF2/ASF in pri-miRNA processing and highlight the potential coordination between splicing control and miRNA-mediated gene repression in gene regulatory networks.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Base Sequence
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • HeLa Cells
  • Humans
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Molecular Sequence Data
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • RNA Interference
  • RNA Splicing*
  • RNA-Binding Proteins
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism
  • Serine-Arginine Splicing Factors

Substances

  • MicroRNAs
  • Nuclear Proteins
  • RNA-Binding Proteins
  • Serine-Arginine Splicing Factors
  • DROSHA protein, human
  • Ribonuclease III