Department of Neurobiology; Tzumin Lee Lab; Graduate School of Biomedical Sciences, Neuroscience Program
Amino Acid Motifs; Amino Acid Sequence; Animals; Animals, Genetically Modified; Cell Adhesion Molecules; Drosophila; Drosophila Proteins; Gene Targeting; Molecular Sequence Data; Morphogenesis; Neurogenesis; Neurons; Protein Structure, Tertiary
Neuroscience and Neurobiology
Drosophila Down syndrome cell adhesion molecule (Dscam) can be variably spliced to encode 152,064 distinct single-pass transmembrane proteins. In addition to 19,008 possible ectodomains and two alternative transmembrane segments, it may carry endodomains containing or lacking exons 19 and 23. Here, we determine the role of Dscam endodomain diversity in neural development. Dscam with full-length endodomain is largely restricted to embryogenesis. In contrast, most Dscams lack exons 19 and 23 at postembryonic stages. As implicated from the expression patterns, removal of Dscam exon 19-containing variants disrupts wiring of embryonic neurons while silencing of Dscam transcripts lacking exon 19 or exon 23 effectively blocks postembryonic neuronal morphogenesis. Furthermore, compared with exon 19-containing Dscam, transgenic Dscam without exon 19 is more efficiently targeted to neurites and more potently suppresses axon bifurcation in Dscam mutant neurons. In sum, Dscam with or without exon 19 in its endodomain is used to govern different stage-specific neuronal morphogenetic processes, possibly due to differences in protein targeting.
DOI of Published Version
J Neurosci. 2009 Feb 11;29(6):1904-14. Link to article on publisher's site
The Journal of neuroscience : the official journal of the Society for Neuroscience
Yu H, Yang JS, Wang J, Huang Y, Lee T. (2009). Endodomain diversity in the Drosophila Dscam and its roles in neuronal morphogenesis. Open Access Articles. https://doi.org/10.1523/JNEUROSCI.5743-08.2009. Retrieved from https://escholarship.umassmed.edu/oapubs/2164