A Drosophila genetic screen yields allelic series of core microRNA biogenesis factors and reveals post-developmental roles for microRNAs
- Peter Smibert1,
- Fernando Bejarano1,
- Dong Wang2,
- Daniel L. Garaulet1,3,
- Jr-Shiuan Yang1,
- Raquel Martin1,3,
- Diane Bortolamiol-Becet1,
- Nicolas Robine1,
- P. Robin Hiesinger2 and
- Eric C. Lai1,4
- 1Department of Developmental Biology, Sloan-Kettering Institute, New York, New York 10065, USA
- 2Department of Physiology and Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA
Abstract
Canonical animal microRNAs (miRNAs) are ∼22-nt regulatory RNAs generated by stepwise cleavage of primary hairpin transcripts by the Drosha and Dicer RNase III enzymes. We performed a genetic screen using an miRNA-repressed reporter in the Drosophila eye and recovered the first reported alleles of fly drosha, an allelic series of its dsRBD partner pasha, and novel alleles of dicer-1. Analysis of drosha mutants provided direct confirmation that mirtrons are independent of this nuclease, as inferred earlier from pasha knockouts. We further used these mutants to demonstrate in vivo cross-regulation of Drosha and Pasha in the intact animal, confirming remarkable conservation of a homeostatic mechanism that aligns their respective levels. Although the loss of core miRNA pathway components is universally lethal in animals, we unexpectedly recovered hypomorphic alleles that gave adult escapers with overtly normal development. However, the mutant photoreceptor neurons exhibited reduced synaptic transmission, without accompanying defects in neuronal development or maintenance. These findings indicate that synaptic function is especially sensitive to optimal miRNA pathway function. These allelic series of miRNA pathway mutants should find broad usage in studies of miRNA biogenesis and biology in the Drosophila system.
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Footnotes
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↵4 Corresponding author.
E-mail laie{at}mskcc.org.
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Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.2983511.
- Received August 10, 2011.
- Accepted August 15, 2011.
- Copyright © 2011 RNA Society