@article{819975db7ab74fd0a84f6aebe3db3f66,
title = "Analysis of Dscam diversity in regulating axon guidance in Drosophila mushroom bodies",
abstract = "Dscam is an immunoglobulin (Ig) superfamily member that regulates axon guidance and targeting in Drosophila. Alternative splicing potentially generates 38,016 isoforms differing in their extracellular Ig and transmembrane domains. We demonstrate that Dscam mediates the sorting of axons in the developing mushroom body (MB). This correlates with the precise spatiotemporal pattern of Dscam protein expression. We demonstrate that MB neurons express different arrays of Dscam isoforms and that single MB neurons express multiple isoforms. Two different Dscam isoforms differing in their extracellular domains introduced as transgenes into single mutant cells partially rescued the mutant phenotype. Expression of one isoform of Dscam in a cohort of MB neurons induced dominant phenotypes, while expression of a single isoform in a single cell did not. We propose that different extracellular domains of Dscam share a common function and that differences in isoforms expressed on the surface of neighboring axons influence interactions between them.",
author = "Zhan, {Xiao Li} and Clemens, {James C.} and Guilherme Neves and Daisuke Hattori and Flanagan, {John J.} and Thomas Hummel and Vasconcelos, {M. Luisa} and Andrew Chess and Zipursky, {S. Lawrence}",
note = "Funding Information: We are grateful to Liqun Luo, Corey S. Goodman, Katsuo Furukubo-Tokunaga, David Lamar, Atsuya Wakabayashi, and Dietmar Schmucker for for stocks and reagents. We thank Tzumin Lee for discussion and sharing data prior to publication. We are in indebted to members of the Zipursky lab for comments on the manuscript; Karen Ronan for the editorial assistance; and Dorian Gunning for expert technical assistance. For the microarray experiments, we thank G. Paradis at the MIT-CCR for help with FACS experiments; and the Center for Microarray Technology at the Whitehead Institute. We thank Yi Sun for use of her real-time PCR machine. This work was supported by postdoctoral fellowships from the Jane Coffin Childs (X.-L.Z.), Helen Hay Whitney (J.C.C) Foundations, the Human Frontiers Science Program (T.H.), an NIH/NRSA (F31) predoctoral fellowship from the NINDS (J.J.F.), a predoctoral fellowship from the Gulbenkian PhD program in Biology and Medicine and the Foundation for Science and Technology in Portugal (M.L.V.), and grants from the NIH (to A.C. and S.L.Z.). S.L.Z. is an Investigator of the Howard Hughes Medical Institute. ",
year = "2004",
month = sep,
day = "2",
doi = "10.1016/j.neuron.2004.07.020",
language = "English (US)",
volume = "43",
pages = "673--686",
journal = "Neuron",
issn = "0896-6273",
publisher = "Cell Press",
number = "5",
}