A novel mechanism for modulating synaptic gene expression:: Differential localization of α-dystrobrevin transcripts in skeletal muscle

被引:30
作者
Newey, SE
Gramolini, AO
Wu, J
Holzfeind, P
Jasmin, BJ
Davies, KE
Blake, DJ
机构
[1] Univ Oxford, Dept Human Anat & Genet, MRC, Funct Genet Unit, Oxford OX1 3QX, England
[2] Univ Ottawa, Fac Med, Dept Cellular & Mol Med, Ottawa, ON K1H 8M5, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1006/mcne.2000.0918
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
alpha -Dystrobrevin is a dystrophin-related and -associated protein that is involved in synapse maturation and is required for normal muscle function. There are three protein isoforms in skeletal muscle, alpha -dystrobrevin-1, -2, and -3 that are encoded by the single alpha -dystrobrevin gene. To understand the role of these proteins in muscle we have investigated the localisation and transcript distribution of the different alpha -dystrobrevin isoforms. alpha -Dystrobrevin-1 and -2 are concentrated at the neuromuscular junction and are both recruited into agrin-induced acetylcholine receptor clusters in cultured myotubes. We also demonstrate that all a-dystrobrevin mRNAs are transcribed from a single promoter in skeletal muscle. However, only transcripts encoding alpha -dystrobrevin-1 are preferentially accumulated at postsynaptic sites. These data suggest that the synaptic accumulation of alpha -dystrobrevin-1 mRNA occurs posttranscriptionally, identifying a novel mechanism for synaptic gene expression. Taken together, these results indicate that different isoforms possess distinct roles in synapse formation and possibly in the pathogenesis of muscular dystrophy.
引用
收藏
页码:127 / 140
页数:14
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