A novel, brain-specific mouse drebrin: cDNA cloning, chromosomal mapping, genomic structure, expression, and functional characterization

被引:26
作者
Jin, MH
Tanaka, S
Sekino, Y
Ren, Y
Yamazaki, H
Kawai-Hirai, R
Kojima, N [1 ]
Shirao, T
机构
[1] Natl Inst Physiol Sci, Neurochem Lab, Okazaki, Aichi 4448585, Japan
[2] Gunma Univ, Sch Med, Dept Neurobiol & Behav, Maebashi, Gumma 3718511, Japan
关键词
actins; cytoskeleton; Dbn1; chromosome; 13; s-drebrin A;
D O I
10.1006/geno.2002.6764
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Drebrin A, a major neuronal actin-binding protein, regulates the dendritic spine shapes of neurons. Here, we have cloned and characterized a novel mouse cDNA clone encoding a truncated form of drebrin A, named s-drebrin A. Analysis of the genomic organization of the mouse drebrin gene (Dbn1), which mapped to the central portion of chromosome 13, revealed that isoforms including s-drebrin A are generated by alternative splicing from a single drebrin gene. The s-drebrin A mRNA was expressed in the brain, but not in non-neuronal tissues. The s-drebrin A expression was barely detected in the embryonic brain, but was upregulated during postnatal development of the brain. Overexpression of GFP-tagged s-drebrin A in fibroblasts showed it to be associated with actin filaments and with changes in actin cytoskeleton organization. These findings suggest that s-drebrin A has a role in spine morphogenesis, possibly by competing the actin-binding activity with drebrin A.
引用
收藏
页码:686 / 692
页数:7
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