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Morquio a syndrome: Cloning, sequence, and structure of the human n- acetylgalactosamine 6-sulfatase (galns) gene

  • C. P. Morris
  • , X. H. Guo
  • , S. Apostolou
  • , J. J. Hopwood
  • , H. S. Scott

Research output: Contribution to journal › Article › peer-review

Abstract

Deficiency of the lysosomal enzyme, N-acetylgalactosamine 6-sulfatase (GALNS; EC 3.1.6.4), results in the storage of the glycosaminoglycans, keratan sulfate and chondroitin 6-sulfate, which leads to the lysosomal storage disorder Morquio A syndrome. Four overlapping genomic clones derived from a chromosome 16-specific gridded cosmid library containing the entire GALNS gene were isolated. The structure of the gene and the sequence of the exon/intron boundaries and the 5' promoter region were determined. The GALNS gene is split into 14 exons spanning approximately 40 kb. The potential promoter for GALNS lacks a TATA box but contains GC box consensus sequences, consistent with its role as a housekeeping gene. The GALNS gene contains an Alu repeat in intron 5 and a VNTR-like sequence in intron 6.

Original languageEnglish
Pages (from-to)652-654
Number of pages3
JournalGenomics
Volume22
Issue number3
DOIs
Publication statusPublished or Issued - Aug 1994
Externally publishedYes

ASJC Scopus subject areas

  • Genetics

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