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Kinesin-II is required for axonal transport of choline acetyltransferase in Drosophila

Raya, Krishanu and Perez, Sharon E. and Yanga, Zhaohuai and Xua, Jenny and Ritchings, Bruce W. and Steller, Hermann and Goldstein, Lawrence S. B. (1999) Kinesin-II is required for axonal transport of choline acetyltransferase in Drosophila. Journal of Cell Biology, 147 (3). pp. 507-518. ISSN 0021-9525. PMCID PMC2151187. doi:10.1083/jcb.147.3.507. https://resolver.caltech.edu/CaltechAUTHORS:RAYjbc99

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Abstract

KLP64D and KLP68D are members of the kinesin-II family of proteins in Drosophila. Immunostaining for KLP68D and ribonucleic acid in situ hybridization for KLP64D demonstrated their preferential expression in cholinergic neurons. KLP68D was also found to accumulate in cholinergic neurons in axonal obstructions caused by the loss of kinesin light chain. Mutations in the KLP64D gene cause uncoordinated sluggish movement and death, and reduce transport of choline acetyltransferase from cell bodies to the synapse. The inviability of KLP64D mutations can be rescued by expression of mammalian KIF3A. Together, these data suggest that kinesin-II is required for the axonal transport of a soluble enzyme, choline acetyltransferase. in a specific subset of neurons in Drosophila. Furthermore, the data lead to the conclusion that the cargo transport requirements of different classes of neurons may lead to upregulation of specific pathways of axonal transport.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1083/jcb.147.3.507DOIArticle
http://www.ncbi.nlm.nih.gov/pmc/articles/pmc2151187/PubMed CentralArticle
Additional Information:© The Rockefeller University Press, 1999. Submitted: 16 February 1999; revised: 24 August 1999; accepted: 13 September 1999. We thank S. Chen for isolating the cDNA clones and sequencing, and Joe Marszalek for providing the KIF3A cDNA. We are grateful to P. Salvaterra, J.T. Littleton, and K. Zinsmaier for providing various antisera. S. Perez was supported by a National Science Foundation postdoctoral fellowship. This project was supported by a grant from the National Institutes of Health to L.S.B. Goldstein. L.S.B. Goldstein and H. Steller are investigators of the Howard Hughes Medical Institute.
Funders:
Funding AgencyGrant Number
NSF Postdoctoral FellowshipUNSPECIFIED
NIHUNSPECIFIED
Howard Hughes Medical Institute (HHMI)UNSPECIFIED
Subject Keywords:Drosophila, kinesin-like proteins, axonal transport, microtubule motors, neurobiology
Issue or Number:3
PubMed Central ID:PMC2151187
DOI:10.1083/jcb.147.3.507
Record Number:CaltechAUTHORS:RAYjbc99
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:RAYjbc99
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:4648
Collection:CaltechAUTHORS
Deposited By: Lindsay Cleary
Deposited On:01 Sep 2006
Last Modified:08 Nov 2021 20:18

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