Calcium/calmodulin-dependent protein kinase IIβ isoform is expressed in motor neurons during axon outgrowth and is part of slow axonal transport

Previously, we identified calcium/calmodulin‐dependent protein kinase IIβ (CaMKIIβ) mRNA in spinal motor neurons with 372 bp inserted in what corresponds to the “association” domain of the protein. This was interesting because known additions and deletions to CaMKIIβ mRNA are usually less than 100 b...

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Published in:Journal of neuroscience research Vol. 67; no. 6; pp. 720 - 728
Main Authors: Lund, Linda M., McQuarrie, Irvine G.
Format: Journal Article
Language:English
Published: New York Wiley Subscription Services, Inc., A Wiley Company 15-03-2002
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Summary:Previously, we identified calcium/calmodulin‐dependent protein kinase IIβ (CaMKIIβ) mRNA in spinal motor neurons with 372 bp inserted in what corresponds to the “association” domain of the protein. This was interesting because known additions and deletions to CaMKIIβ mRNA are usually less than 100 bp in size and found in the “variable” region. Changes in the association domain of CaMKIIβ could influence substrate specificity, activity or intracellular targeting. We show that three variations of this insert are found in CNS neurons or sciatic motor neurons of Sprague–Dawley rats. We used PCR and nucleic acid sequencing to identify inserts of 114, 243, or 372 bases. We also show that addition of the 372 bases is associated with outgrowth of the axon (the standard CaMKIIβ downregulates when axon outgrowth occurs). Radiolabeling, immunoblots, and 2D PAGE identified this larger CaMKIIβ as part of the group of soluble proteins moving at the slowest rate of axonal transport (SCa) in sciatic motor neurons (∼1 mm/day). This group is composed mainly of structural proteins (e.g., tubulin) used to assemble the cytoskeleton of regrowing axons. Published 2002 Wiley‐Liss, Inc.
Bibliography:istex:6FF1E63D232A40E296A0800D68E05D75B4C5A087
NINDS - No. NS09803-02
Medical Research Service of the Department of Veteran Affairs
ark:/67375/WNG-X6SW16MZ-Q
This article is a US Government work and, as such, is in the public domain in the United States of America.
ArticleID:JNR10162
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0360-4012
1097-4547
DOI:10.1002/jnr.10162