Spatial regulation of microRNA gene expression in the Drosophila embryo
- Frédéric Biemar*,
- Robert Zinzen*,
- Matthew Ronshaugen*,
- Victor Sementchenko†,
- J. Robert Manak†, and
- Michael S. Levine*,‡
- *Division of Genetics and Development, Department of Molecular Cell Biology, Center for Integrative Genomics, University of California, Berkeley, CA 94720; and †Affymetrix, Inc., Santa Clara, CA 95051
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Contributed by Michael S. Levine, September 8, 2005
Abstract
MicroRNAs (miRNAs) regulate posttranscriptional gene activity by binding to specific sequences in the 3′ UTRs of target mRNAs. A number of metazoan miRNAs have been shown to exhibit tissue-specific patterns of expression. Here, we investigate the possibility that localized expression is mediated by tissue-specific enhancers, comparable to those seen for protein-coding genes. Two miRNA loci in Drosophila melanogaster are investigated, the mir-309–6 polycistron (8-miR) and the mir-1 gene. The 8-miR locus contains a cluster of eight distinct miRNAs that are transcribed in a common precursor RNA. The 8-miR primary transcript displays a dynamic pattern of expression in early embryos, including repression at the anterior and posterior poles. An 800-bp 5′ enhancer was identified that recapitulates this complex pattern when attached to a RNA polymerase II core promoter fused to a lacZ-reporter gene. The miR-1 locus is specifically expressed in the mesoderm of gastrulating embryos. Bioinformatics methods were used to identify a mesoderm-specific enhancer located ≈5 kb 5′ of the miR-1 transcription unit. Evidence is presented that the 8-miR enhancer is regulated by the localized Huckebein repressor, whereas miR-1 is activated by Dorsal and Twist. These results provide evidence that restricted activities of the 8-miR and miR-1 miRNAs are mediated by classical tissue-specific enhancers.
Footnotes
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↵ ‡ To whom correspondence should be addressed. E-mail: mlevine{at}berkeley.edu.
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Author contributions: F.B. and M.S.L. designed research; F.B. and R.Z. performed research; V.S. and J.R.M. contributed new reagents/analytical tools; F.B., R.Z., M.R., and M.S.L. analyzed data; and F.B. and M.S.L. wrote the paper.
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Abbreviations: Hkb, Huckebein; miRNA, microRNA; Htl, Heartless.
- Copyright © 2005, The National Academy of Sciences





