Characterization of the human α-synuclein gene: Genomic structure, transcription start site, promoter region and polymorphisms

被引:37
作者
Xia, Yu [1 ]
Saitoh, Tsunao [1 ]
Ueda, Kenji [1 ,3 ]
Tanaka, Seigo [1 ,4 ]
Chen, Xiaohua [1 ]
Hashimoto, Makoto [1 ]
Hsu, Leigh [1 ]
Conrad, Chris [1 ,5 ]
Sundsmo, Mary [1 ]
Yoshimoto, Makoto [1 ,6 ]
Thal, Leon [1 ]
Katzman, Robert [1 ]
Masliah, Eliezer [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
[3] Tokyo Inst Psychiat, Dept Neurochem, Setagaya Ku, Tokyo 1568585, Japan
[4] Kyoto Univ, Inst Chem Res, Uji, Kyoto 611, Japan
[5] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[6] Taisho Pharmaceut Co Ltd, Dept Mol Biol, Omiya, Saitama 330, Japan
关键词
D O I
10.3233/JAD-2001-3508
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The human NACP/alpha-synuclein gene has been cloned. This gene consists of 6 exons ranging in size from 42 to 1110 bp. The translation start codon ATG is encoded by exon 2 and the stop codon TAA is encoded by exon 6. The non-A beta component of Alzheimer's disease amyloid (NAC) is encoded by exon 4. The two previously reported minor isoforms of NACP/alpha-synuclein, NACP112 [29] and NACP126 [6], are alternatively spliced products, in which exon 5 and exon 3 are spliced out, respectively. Exon 1 was found to have different splicing sites, producing different 5'-untranslated sequences in the cDNAs. A previously reported dinucleotide repeat polymorphic marker has been mapped to 8kb upstream of the transcription start site. A highly TC-rich sequence in intron 4 was found to be polymorphic by length and four alleles, A0, A1, A2 and B have been identified in the Caucasian population. Genotyping this polymorphism among pure Alzheimer's, Lewy body variant and Parkinson's subjects and aged normal control subjects did not reveal any significant differences.
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收藏
页码:485 / 494
页数:10
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