WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience PeproTech - Your Source for Neuroscience Research Reagents
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hong, C. S.
Right arrow Articles by Ganetzky, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hong, C. S.
Right arrow Articles by Ganetzky, B.

 Previous Article  |  Next Article 

Journal of Neuroscience, Vol 14, 5160-5169, Copyright © 1994 by Society for Neuroscience


ARTICLE

Spatial and temporal expression patterns of two sodium channel genes in Drosophila

CS Hong and B Ganetzky
Laboratory of Genetics, University of Wisconsin, Madison 53706.

Genetic and molecular studies have identified two different sodium channel genes in Drosophila, para and DSC1. The functional contributions of the para-encoded channel have been inferred from analysis of mutant phenotypes. However, no mutations of DSC1 have been identified, so the in vivo functions of the channel it encodes are not yet known. To learn more about the possible functions of DSC1 in the Drosophila nervous system compared with those of para, we have characterized the expression patterns of these two sodium channel genes at embryonic, larval, pupal, and adult stages by tissue in situ hybridization, para encodes the predominant type of sodium channel and is ubiquitously transcribed throughout the CNS and PNS at all developmental stages. The expression pattern of DSC1 is very different from para during embryonic and larval stages during which there are very few DSC1-expressing cells in either the CNS or PNS. Double- labeling studies suggest that some of these cells are non-neuronal. However, in pupal and adult stages, para and DSC1 have completely overlapping patterns of expression in the CNS and retina. In the pupal and adult, PNS expression of these genes is still distinct because only para transcripts are detected in wing sensory neurons. The strong and widespread expression of DSC1 in the CNS of pupae and adults suggests that the DSC1 channels are likely to provide an important function in neurons during these stages. Since most, if not all, neurons in the pupal and adult CNS express both para and DSC1, these two sodium channel genes probably subserve distinct functions within these cells. Our results provide the background for elucidating the respective in vivo contributions of para and DSC1 to neuronal excitability and for dissecting the regulatory mechanisms that underlie their different patterns of expression.


This article has been cited by other articles:


Home page
GeneticsHome page
H. A. Lindsay, R. Baines, R. ffrench-Constant, K. Lilley, H. T. Jacobs, and K. M. C. O'Dell
The Dominant Cold-Sensitive Out-Cold Mutants of Drosophila melanogaster Have Novel Missense Mutations in the Voltage-Gated Sodium Channel Gene paralytic
Genetics, October 1, 2008; 180(2): 873 - 884.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Lee and C.-F. Wu
Genetic Modifications of Seizure Susceptibility and Expression by Altered Excitability in Drosophila Na+ and K+ Channel Mutants
J Neurophysiol, November 1, 2006; 96(5): 2465 - 2478.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. J. Mee, E. C. G. Pym, K. G. Moffat, and R. A. Baines
Regulation of Neuronal Excitability through Pumilio-Dependent Control of a Sodium Channel Gene
J. Neurosci., October 6, 2004; 24(40): 8695 - 8703.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
E. S. Montana and J. T. Littleton
Characterization of a hypercontraction-induced myopathy in Drosophila caused by mutations in Mhc
J. Cell Biol., March 29, 2004; 164(7): 1045 - 1054.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
N. H. Kulkarni, A. H. Yamamoto, K. O. Robinson, T. F. C. Mackay, and R. R. H. Anholt
The DSC1 Channel, Encoded by the smi60E Locus, Contributes to Odor-Guided Behavior in Drosophila melanogaster
Genetics, August 1, 2002; 161(4): 1507 - 1516.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
H. A. Nash
In vivo genetics of anaesthetic action
Br. J. Anaesth., July 1, 2002; 89(1): 143 - 155.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. F. Lopreato, Y. Lu, A. Southwell, N. S. Atkinson, D. M. Hillis, T. P. Wilcox, and H. H. Zakon
Evolution and divergence of sodium channel genes in vertebrates
PNAS, June 19, 2001; 98(13): 7588 - 7592.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. Wicher
Peptidergic Modulation of an Insect Na+ Current: Role of Protein Kinase A and Protein Kinase C
J Neurophysiol, January 1, 2001; 85(1): 374 - 383.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
L. Yuan and B. Ganetzky
A Glial-Neuronal Signaling Pathway Revealed by Mutations in a Neurexin-Related Protein
Science, February 26, 1999; 283(5406): 1343 - 1345.
[Abstract] [Full Text]


Home page
J. Neurosci.Home page
S. A. Titus, J. W. Warmke, and B. Ganetzky
The Drosophila erg K+ Channel Polypeptide Is Encoded by the Seizure Locus
J. Neurosci., February 1, 1997; 17(3): 875 - 881.
[Abstract] [Full Text] [PDF]



-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-