4.8 Article

Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC)

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 105, 期 5, 页码 673-681

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI5826

关键词

-

资金

  1. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT [R01HD031920] Funding Source: NIH RePORTER
  2. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG000313] Funding Source: NIH RePORTER
  3. NHGRI NIH HHS [HG00313] Funding Source: Medline
  4. NICHD NIH HHS [HD31920] Funding Source: Medline

向作者/读者索取更多资源

Mucolipidosis IIIC, or variant pseudo-Hurler polydystrophy, is an autosomal recessive disease of lysosomal hydrolase trafficking. Unlike the related diseases, mucolipidosis II and IIIA, the enzyme affected in mucolipidosis IIIC (N-Acetylglucosamine-1-phosphotransferase [GlcNAc-phosphotransferase]) retains full transferase activity on synthetic substrates but lacks activity on lysosomal hydrolases. Bovine GlcNAc-phosphotransferase has recently been isolated as a multisubunit enzyme with the subunit structure alpha(2)beta(2)gamma(2). We cloned the cDNA for the human gamma-subunit and localized its gene to chromosome 16p. We also showed, in a large multiplex Druze family that exhibits this disorder, that MLIIIC also maps to this chromosomal region. Sequence analysis of the gamma-subunit cDNA in patients from 3 families identified a frameshift mutation, in codon 167 of the gamma subunit, that segregated with the disease, indicating MLIIIC results from mutations in the phosphotransferase gamma-subunit gene. This is to our knowledge the first description of the molecular basis for a human mucolipidosis and suggests that the gamma subunit functions in lysosomal hydrolase recognition.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据