Mucopolysaccharidosis type I: Characterization of novel mutations affecting α-L-iduronidase activity

G. J. Lee-Chen*, S. P. Lin, Y. F. Tang, Y. W. Chin

*此作品的通信作者

研究成果: 雜誌貢獻期刊論文同行評審

22 引文 斯高帕斯(Scopus)

摘要

α-L-Iduronidase (IDUA) deficiency (mucopolysaccharidosis type 1, MPS I) involves a broad spectrum of clinical severity ranging from a severe Hurler syndrome through an intermediate Hurler-Scheie syndrome to a mild Scheie syndrome. To date, a number of mutations of the IDUA gene are known in Hurler syndrome, but only a few in Hurler-Scheie or Scheie syndrome. The characterization of novel mutations in two patients with the Hurler-Scheie syndrome is reported on. The novel R619G mutation (C-G transversion in codon 619) was apparently homozygous. In transfected COS-7 cells, R619G caused significant reduction in enzyme activity (1.5% of normal activity), although it did not cause significant reduction in IDUA mRNA or protein level. Conversely, the previously described homozygous T364M mutation (C-T transition in codon 364) caused a decrease in the level of IDUA mRNA. Studies inhibiting RNA synthesis with actinomycin D or inhibiting protein synthesis with cycloheximide demonstrate that the decrease in the latter mutation is attributable to an increased rate of mRNA decay. By examining the stability of IDUA mRNA and protein, studies provide better insight into the effect of mutation on IDUA activity.

原文英語
頁(從 - 到)66-70
頁數5
期刊Clinical Genetics
56
發行號1
DOIs
出版狀態已發佈 - 1999

ASJC Scopus subject areas

  • 遺傳學
  • 遺傳學(臨床)

指紋

深入研究「Mucopolysaccharidosis type I: Characterization of novel mutations affecting α-L-iduronidase activity」主題。共同形成了獨特的指紋。

引用此