MOLECULAR INVESTIGATION OF PEROXISOMAL beta-OXIDATION ENZYME DEFICIENCIES
MOLECULAR INVESTIGATION OF PEROXISOMAL beta-OXIDATION ENZYME DEFICIENCIES
批准号:
06670781
负责人:
SUZUKI Yasuyuki
金额:
$1.02万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995
中文摘要
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英文摘要
cDNAs for human acyl-CoA oxidase and bifunctional enzyme were cloned. Acyl-CoA oxidase cDNA has SKL motif and encodes 661 amino acids with high homology to rat enzyme. Consanguineous siblings with acyl-CoA oxidase deficieency had a homozygous exonic point mutation which resulted in an amino acid substitution (M278V). Cloned cDNA for bifunctional enzyme encodes 772 amino acids. A patient with bifunctional enzyme deficiency had a point mutation (A274T). These results will facilitate DNA diagnosis and gene therapy for these disorders.
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鈴木康之、下沢伸行、折居忠夫: "遺伝子診断実践ガイド" 中外医学社, 485 (1995)
Yasuyuki Suzuki、Nobuyuki Shimosawa、Tadao Orii:“遗传诊断实用指南”Chugai Igakusha,485(1995)
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Atsushi Uchiyama: "Identification of a nonsense mutation in ALD protein cDNA from a patiant with adrenoleukodystrophy." Biochem.Biophys,Res.Commun.198. 632-636 (1994)
Atsushi Uchiyama:“从一名肾上腺脑白质营养不良患者身上鉴定出 ALD 蛋白 cDNA 中的无义突变。”
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Y Suzuki,N Shimozawa,et al.: "Prenatal diagnosis of peroxisomal disorders.Biochemical and immunocytochemical studies on peroxisomes in human amniocytes." Brain&Development. 16. 27-31 (1994)
Y Suzuki,N Shimozawa 等人:“过氧化物酶体疾病的产前诊断。人羊水细胞过氧化物酶体的生化和免疫细胞化学研究。”
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Y Suzuki,N Shimozawa,et al.: "Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochenical studies on peroxisomes in human amniocytes." Brain & Development. 16. 27-31 (1994)
Y Suzuki,N Shimozawa 等人:“过氧化物酶体疾病的产前诊断。人类羊水细胞过氧化物酶体的生化和免疫细胞化学研究。”
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Yasuyuki Suzuki: "Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiaency with detectable enzyme protein" Am.J.Hum.Genet.54. 36-43 (1994)
Yasuyuki Suzuki:“过氧化物酶体酰基辅酶 A 氧化酶缺乏症和双功能酶缺乏症的新亚型,可检测到酶蛋白”Am.J.Hum.Genet.54。
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