TY - JOUR
T1 - A new prospero and microRNA-279 pathway restricts CO 2 receptor neuron formation
AU - Hartl, Marion
AU - Loschek, Laura F.
AU - Stephan, Daniel
AU - Siju, K. P.
AU - Knappmeyer, Christiane
AU - Kadow, Ilona C.Grunwald
PY - 2011/11/2
Y1 - 2011/11/2
N2 - CO 2 sensation represents an interesting example of nervous system and behavioral evolutionary divergence. The underlying molecular mechanisms, however, are not understood. Loss of microRNA-279 in Drosophila melanogaster leads to the formation of a CO 2 sensory system partly similar to the one of mosquitoes. Here, we show that a novel allele of the pleiotropic transcription factor Prospero resembles the miR-279 phenotype. We use a combination of genetics and in vitro and in vivo analysis to demonstrate that Pros participates in the regulation of miR-279 expression, and that reexpression of miR-279 rescues the pros CO 2 neuron phenotype. We identify common target molecules of miR-279 and Pros in bioinformatics analysis, and show that overexpression of the transcription factors Nerfin-1 and Escargot (Esg) is sufficient to induce formation of CO 2 neurons on maxillary palps. Our results suggest that Prospero restricts CO 2 neuron formation indirectly via miR-279 and directly by repressing the shared target molecules, Nerfin-1 and Esg, during olfactory system development. Given the important role of Pros in differentiation of the nervous system, we anticipate that miR-mediated signal tuning represents a powerful method for olfactory sensory system diversification during evolution.
AB - CO 2 sensation represents an interesting example of nervous system and behavioral evolutionary divergence. The underlying molecular mechanisms, however, are not understood. Loss of microRNA-279 in Drosophila melanogaster leads to the formation of a CO 2 sensory system partly similar to the one of mosquitoes. Here, we show that a novel allele of the pleiotropic transcription factor Prospero resembles the miR-279 phenotype. We use a combination of genetics and in vitro and in vivo analysis to demonstrate that Pros participates in the regulation of miR-279 expression, and that reexpression of miR-279 rescues the pros CO 2 neuron phenotype. We identify common target molecules of miR-279 and Pros in bioinformatics analysis, and show that overexpression of the transcription factors Nerfin-1 and Escargot (Esg) is sufficient to induce formation of CO 2 neurons on maxillary palps. Our results suggest that Prospero restricts CO 2 neuron formation indirectly via miR-279 and directly by repressing the shared target molecules, Nerfin-1 and Esg, during olfactory system development. Given the important role of Pros in differentiation of the nervous system, we anticipate that miR-mediated signal tuning represents a powerful method for olfactory sensory system diversification during evolution.
UR - http://www.scopus.com/inward/record.url?scp=80155171400&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.2592-11.2011
DO - 10.1523/JNEUROSCI.2592-11.2011
M3 - Article
C2 - 22049409
AN - SCOPUS:80155171400
SN - 0270-6474
VL - 31
SP - 15660
EP - 15673
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 44
ER -