@article {760066,
	title = {Functional screening identifies miR-315 as a potent activator of Wingless signaling.},
	journal = {Proc Natl Acad Sci U S A},
	volume = {104},
	number = {46},
	year = {2007},
	month = {2007 Nov 13},
	pages = {18151-6},
	abstract = {
	The existence of vast regulatory networks mediated by microRNAs (miRNAs) suggests broad potential for miRNA dysfunction to contribute to disease. However, relatively few miRNA-target interactions are likely to make detectable contributions to phenotype, and effective strategies to identify these few interactions are currently wanting. We hypothesized that signaling cascades represent critical points of susceptibility to miRNA dysfunction, and we developed a strategy to test this theory by using quantitative cell-based screens. Here we report a screen for miRNAs that affect the Wingless (Wg) pathway, a conserved pathway that regulates growth and tissue specification. This process identified ectopic miR-315 as a potent and specific activator of Wg signaling, an activity that we corroborated in transgenic animals. This miR-315 activity was mediated by direct inhibition of Axin and Notum, which encode essential, negatively acting components of the Wg pathway. Genetic interaction tests substantiated both of these genes as key functional targets of miR-315. The ability of ectopic miR-315 to activate Wg signaling was not a trivial consequence of predicted miRNA-target relationships because other miRNAs with conserved sites in the Axin 3{\textquoteright} UTR neither activated Wg outputs nor inhibited an Axin sensor. In summary, activity-based screening can selectively identify miRNAs whose deregulation can lead to interpretable phenotypic consequences.

},
	keywords = {3{\textquoteright} Untranslated Regions, Animals, Animals, Genetically Modified, Base Sequence, DNA Primers, Drosophila, Drosophila Proteins, MicroRNAs, Proto-Oncogene Proteins, Signal Transduction, Wnt1 Protein},
	issn = {1091-6490},
	doi = {10.1073/pnas.0706673104},
	author = {Silver, Serena J and Hagen, Joshua W and Okamura, Katsutomo and Perrimon, Norbert and Lai, Eric C}
}
