A splice variant of the neurotrophin receptor trkB with increased specificity for brain-derived neurotrophic factor

被引:109
作者
Strohmaier, C
Carter, BD
Urfer, R
Barde, YA
Dechant, G
机构
[1] MAX PLANCK INST PSYCHIAT,DEPT NEUROBIOCHEM,D-82152 PLANEGG,GERMANY
[2] GENENTECH INC,S SAN FRANCISCO,CA 94080
关键词
alternative splicing; genomic organization; neurotrophin receptors; neurotrophins; protein domains;
D O I
10.1002/j.1460-2075.1996.tb00698.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The trkB gene codes for a receptor tyrosine kinase, which is essential for the development of the peripheral nervous system. This receptor can be activated by three different neurotrophins: BDNF, NT-4/5 and NT-3. The extracellular domain of trkB was found to be encoded in 10 exons corresponding to receptor subdomains previously identified on the basis of protein sequence comparisons. Exon 9 was skipped in a novel tyrosine kinase transcript of the trkB gene, designated ctrkB-Short (ctrkB-S). While the previously described trkB receptor ctrkB-Long (ctrkB-L) and trkB-S receptors were activated similarly by BDNF, trkB-S interacted poorly with NT-4/5 and NT-3 as measured by ligand binding, ligand-induced autophosphorylation and ligand-dependent activation of p21(ras). Efficient activation of ctrkB-S by NT-3 was restored by a single amino acid replacement in NT-3 (D15A). Both trkB-L and trkB-S transcripts were detected in embryonic neurons.
引用
收藏
页码:3332 / 3337
页数:6
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