Dynamic isomiR regulation in Drosophila development

  1. John S. Mattick
  1. Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia

Abstract

Several recent reports have demonstrated that microRNAs (miRNAs) can exhibit heterogeneous ends and post-transcriptional nontemplate 3′ end additions of uridines or adenosines. Using two small RNA deep-sequencing data sets, we show here that these miRNA isoforms (isomiRs) are differentially expressed across Drosophila melanogaster development and tissues. Specifically, we demonstrate that: (1) nontemplate nucleotide additions of adenosines to miRNA 3′ ends are highly abundant in early development; (2) a subset of miRNAs with nontemplate 3′ Us are expressed in adult tissues; and (3) the size of at least eight “mature” (unmodified) miRNAs varies in a life-cycle or tissue-specific manner. These results suggest that subtle variability in isomiR expression, which is widely thought to be the result of inexact Dicer processing, is regulated and biologically meaningful. Indeed, a subset of the miRNAs enriched for 3′ adenosine additions during early embryonic development, including miR-282 and miR-312, show enrichment for target sites in developmental genes that are expressed during late embryogenesis, suggesting that nontemplate additions increase miRNA stability or strengthen miRNA:target interactions. This work suggests that isomiR expression is an important aspect of miRNA biology, which warrants further investigation.

Keywords

Footnotes

  • Reprint requests to: John S. Mattick, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia; e-mail: j.mattick{at}imb.uq.edu.au; fax: 61-7-3346-2111.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.2379610.

  • Received February 5, 2010.
  • Accepted July 21, 2010.
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