Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0004461,
umls-concept:C0017262,
umls-concept:C0017337,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0079429,
umls-concept:C0162610,
umls-concept:C0439849,
umls-concept:C0445223,
umls-concept:C1171362,
umls-concept:C1314939,
umls-concept:C1515670,
umls-concept:C1518294,
umls-concept:C1552599,
umls-concept:C1704787
|
pubmed:issue |
10
|
pubmed:dateCreated |
1995-12-4
|
pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/T06278,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/T06728,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/T07524,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/T08129,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/T09404,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Z46882
|
pubmed:abstractText |
Using two-dimensional gel electrophoresis we previously identified membrane-associated proteins that are upregulated over the course of neurogenesis. One of these, TOAD-64 (Turned On After Division, 64 kDa), is expressed immediately after neuronal birth and is dramatically downregulated in the adult. The gene encoding TOAD-64 has now been cloned, and its sequence shows homology to the unc-33 gene from C. elegans, mutations in which lead to aberrations in axon outgrowth. Northern and in situ hybridization show that TOAD-64 mRNA is enriched in the nervous system and is developmentally regulated in parallel with the protein. The expression of the TOAD-64 protein and gene coincident with initial neuronal differentiation and the downregulation when the majority of axon growth is complete suggests a role in axon elaboration. Three additional lines of evidence support this possibility: TOAD-64 is upregulated following neuronal induction of P19 and PC12 cells; the protein is found in lamellipodia and filopodia of growth cones; and axotomy of the sciatic nerve induces reexpression. While the sequence of TOAD-64 lacks a signal sequence and therefore is likely to encode a cytoplasmic protein, biochemical experiments demonstrate that the protein is tightly, but noncovalently, associated with membranes. The data presented here suggest that TOAD-64 could be a central element in the machinery underlying axonal outgrowth and pathfinding, perhaps playing a role in the signal transduction processes that permit growing axons to choose correct routes and targets.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0270-6474
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
15
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
6757-66
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:7472434-Aging,
pubmed-meshheading:7472434-Amino Acid Sequence,
pubmed-meshheading:7472434-Animals,
pubmed-meshheading:7472434-Axons,
pubmed-meshheading:7472434-Base Sequence,
pubmed-meshheading:7472434-Caenorhabditis elegans,
pubmed-meshheading:7472434-Cell Differentiation,
pubmed-meshheading:7472434-Cell Line,
pubmed-meshheading:7472434-Cloning, Molecular,
pubmed-meshheading:7472434-Denervation,
pubmed-meshheading:7472434-Gene Expression,
pubmed-meshheading:7472434-Membrane Proteins,
pubmed-meshheading:7472434-Molecular Sequence Data,
pubmed-meshheading:7472434-Nervous System,
pubmed-meshheading:7472434-Neurons,
pubmed-meshheading:7472434-PC12 Cells,
pubmed-meshheading:7472434-RNA, Messenger,
pubmed-meshheading:7472434-Rats
|
pubmed:year |
1995
|
pubmed:articleTitle |
TOAD-64, a gene expressed early in neuronal differentiation in the rat, is related to unc-33, a C. elegans gene involved in axon outgrowth.
|
pubmed:affiliation |
Section of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|