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B型Sanfilippo综合征(黏多糖贮积症IIIB)中的分子缺陷

Molecular defects in Sanfilippo syndrome type B (mucopolysaccharidosis IIIB).

作者信息

Beesley C E, Jackson M, Young E P, Vellodi A, Winchester B G

机构信息

Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, University College London, London, UK.

出版信息

J Inherit Metab Dis. 2005;28(5):759-67. doi: 10.1007/s10545-005-0093-y.

Abstract

Sanfilippo syndrome type B (mucopolysaccharidosis IIIB) is an autosomal recessive disease that is caused by the deficiency of the lysosomal enzyme alpha-N-acetylglucosaminidase (NAGLU). NAGLU is involved in the degradation of the glycosaminoglycan (GAG) heparan sulphate, and a deficiency results in the accumulation of partially degraded GAGs inside lysosomes. Early clinical symptoms include hyperactivity, aggressiveness and delayed development, followed by progressive mental deterioration, although there are a small number of late-onset attenuated cases. The gene for NAGLU has been fully characterized and we report the molecular analysis of 18 Sanfilippo B families. In total, 34 of the 36 mutant alleles were characterized in this study and 20 different mutations were identified including 8 novel changes (R38W, V77G, 407-410del4, 703delT, A246P, Y335C, 1487delT, E639X). The four novel missense mutations were transiently expressed in Chinese hamster ovary cells and all were shown to decrease the NAGLU activity markedly, although A246P did produce 12.7% residual enzyme activity.

摘要

B型Sanfilippo综合征(黏多糖贮积症IIIB型)是一种常染色体隐性疾病,由溶酶体酶α-N-乙酰氨基葡萄糖苷酶(NAGLU)缺乏引起。NAGLU参与糖胺聚糖(GAG)硫酸乙酰肝素的降解,其缺乏会导致溶酶体内部分降解的GAGs积累。早期临床症状包括多动、攻击性和发育迟缓,随后是进行性智力衰退,不过也有少数迟发性症状较轻的病例。NAGLU基因已得到充分表征,我们报告了对18个Sanfilippo B家族的分子分析。本研究共鉴定了36个突变等位基因中的34个,发现了20种不同的突变,包括8种新变化(R38W、V77G、407-410del4、703delT、A246P、Y335C、1487delT、E639X)。这四种新的错义突变在中国仓鼠卵巢细胞中瞬时表达,结果显示所有突变均显著降低NAGLU活性,不过A246P确实产生了12.7%的残余酶活性。

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