PRIMARY STRUCTURE OF HUMAN AMPHIPHYSIN, THE DOMINANT - AUTOANTIGEN OF PARANEOPLASTIC STIFF-MAN SYNDROME, AND MAPPING OF ITS GENE (AMPH) TO CHROMOSOME 7P13-P14

被引:28
作者
YAMAMOTO, R
LI, X
WINTER, S
FRANCKE, U
KILIMANN, MW
机构
[1] RUHR UNIV BOCHUM,FAK MED,INST PHYSIOL CHEM,D-44780 BOCHUM,GERMANY
[2] STANFORD UNIV,MED CTR,HOWARD HUGHES MED INST,STANFORD,CA 94305
[3] STANFORD UNIV,MED CTR,DEPT GENET,STANFORD,CA 94305
[4] STANFORD UNIV,MED CTR,DEPT PEDIAT,STANFORD,CA 94305
关键词
D O I
10.1093/hmg/4.2.265
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
Amphiphysin is a protein peripherally associated with synaptic vesicles. It is expressed in many neurons, certain endocrine cell types, and spermatocytes. Autoantibodies against amphiphysin occur in patients afflicted with a rare neurologic autoimmune disease, paraneoplastic Stiff-Man syndrome. To provide a basis for the understanding of anti-amphiphysin autoimmunity, we have cloned cDNAs and determined the primary structure of human amphiphysin. Comparison with chicken amphiphysin defines domains of low and high amino acid sequence conservation. As a candidate for heritable disorders of the nervous system, endocrine tissues or male fertility, the human amphiphysin gene was mapped to chromosome 7, region p13-p14.
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页码:265 / 268
页数:4
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