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MicroRNA sponges: Progress and possibilities

  1. Phillip A. Sharp1,2
  1. 1Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
  2. 2Koch Institute for Integrative Cancer Research, Cambridge, Massachusetts 02139, USA

Abstract

The microRNA (miRNA) “sponge” method was introduced three years ago as a means to create continuous miRNA loss of function in cell lines and transgenic organisms. Sponge RNAs contain complementary binding sites to a miRNA of interest, and are produced from transgenes within cells. As with most miRNA target genes, a sponge's binding sites are specific to the miRNA seed region, which allows them to block a whole family of related miRNAs. This transgenic approach has proven to be a useful tool to probe miRNA functions in a variety of experimental systems. Here we will discuss the ways sponge and related constructs can be optimized and review recent applications of this method with particular emphasis on stable expression in cancer studies and in transgenic animals.

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  • Reprint requests to: Phillip A. Sharp, Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA; e-mail:sharppa{at}mit.edu; fax: (617) 253-3867.

  • Article published online ahead of print. Article and publication date are athttp://www.rnajournal.org/cgi/doi/10.1261/rna.2414110.

  • Copyright © 2010 RNA Society
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  1. Published in AdvanceSeptember 20, 2010, doi:10.1261/rna.2414110 RNA 16: 2043-2050Copyright © 2010 RNA Society
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