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猫 VI 型黏多糖贮积症。重组 N-乙酰半乳糖胺 4-硫酸酯酶的特性及导致该疾病的突变鉴定。

Feline mucopolysaccharidosis type VI. Characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the disease.

作者信息

Yogalingam G, Litjens T, Bielicki J, Crawley A C, Muller V, Anson D S, Hopwood J J

机构信息

Lysosomal Diseases Research Unit, Department of Chemical Pathology, Women's and Children's Hospital, 72 King William Road, North Adelaide, 5006 South Australia, Australia.

出版信息

J Biol Chem. 1996 Nov 1;271(44):27259-65. doi: 10.1074/jbc.271.44.27259.

Abstract

Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive disease caused by a deficiency of N-acetylgalactosamine 4-sulfatase (4S) leading to the lysosomal accumulation and urinary excretion of dermatan sulfate. MPS VI has also been described in the Siamese cat. As an initial step toward enzyme replacement therapy with recombinant feline 4S (rf4S) in MPS VI cats, the feline 4S cDNA was isolated and expressed in CHO-KI cells and rf4S was immunopurified from the culture medium. SDS-polyacrylamide gel electrophoresis analysis showed that the precursor form of immunopurified rf4S was a 66-kDa polypeptide that underwent maturation to a 43-44-kDa polypeptide. Endocytosis of rf4S by cultured feline MPS VI myoblasts was predominantly mediated by a mannose 6-phosphate receptor and resulted in the correction of dermatan sulfate storage. The mutation causing feline MPS VI was identified as a base substitution at codon 476, altering a leucine codon to a proline (L476P). The L476P allele displayed no detectable 4S activity when expressed in CHO-KI cells and was observed only as a "precursor" polypeptide that was not secreted into the medium. Identification of the mutation has allowed the development of a rapid PCR-based screening method to genotype individuals within the cat colony.

摘要

黏多糖贮积症 VI 型(MPS VI)是一种常染色体隐性疾病,由 N - 乙酰半乳糖胺 4 - 硫酸酯酶(4S)缺乏引起,导致硫酸皮肤素在溶酶体中蓄积并经尿液排泄。MPS VI 在暹罗猫中也有报道。作为用重组猫 4S(rf4S)对 MPS VI 型猫进行酶替代疗法的第一步,分离了猫 4S cDNA 并在 CHO - K1 细胞中表达,然后从培养基中免疫纯化 rf4S。十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分析表明,免疫纯化的 rf4S 的前体形式是一条 66 kDa 的多肽,它会成熟为一条 43 - 44 kDa 的多肽。培养的猫 MPS VI 成肌细胞对 rf4S 的内吞作用主要由甘露糖 6 - 磷酸受体介导,并导致硫酸皮肤素蓄积得到纠正。导致猫 MPS VI 的突变被鉴定为密码子 476 处的碱基替换,将亮氨酸密码子改变为脯氨酸(L476P)。L476P 等位基因在 CHO - K1 细胞中表达时未检测到 4S 活性,且仅观察到作为“前体”多肽未分泌到培养基中。该突变的鉴定使得能够开发一种基于聚合酶链反应的快速筛选方法,对猫群体中的个体进行基因分型。

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