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.
引用
收藏
页码:485 / 494
页数:10
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