Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia.

Abstract

UNLABELLED:

A total of 22 Japanese patients with hypophosphatasia were included in a study analysing the relationship between mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene and the severity of the phenotype in Japanese patients with hypophosphatasia. The enzymatic activity of some of the identified mutant TNSALP proteins was also examined using corresponding expression vectors. Eighteen mutations, including 6 novel ones, were identified in the patients. Among them, the common mutations were F310L and T1559del. Of note, five patients with F310L mutation in one of the alleles exhibited a relatively mild phenotype without respiratory complications despite its perinatal onset. In contrast, the T1559del mutation is associated with perinatal lethal and infantile forms when not found in patients with the F310L mutation. The genotype-phenotype relationship was, to some extent, consistent with the enzymatic activity of the mutant ALP proteins; mutations K207E and G409C found in a surviving case of infantile hypophosphatasia, as well as F310L, retained some residual activities, whereas T1559del caused a complete loss of activity.

CONCLUSION:

In Japanese patients, the common mutations F310L and T1559del are associated with the relatively mild and lethal forms of hypophosphatasia, respectively. Our results may enhance the importance of genotyping patients with hypophosphatasia to predict their prognosis.

• Authors: Toshimi Michigami, Takayuki Uchihashi, Akira Suzuki, Kanako Tachikawa, Shigeo Nakajima, Keiichi Ozono
• Journal: European journal of pediatrics (Eur J Pediatr) Vol. 164 Issue 5 Pg. 277-82 (May 2005) ISSN: 0340-6199 [Print] Germany
• PMID: 15660230 (Publication Type: Journal Article)

Chemical References

• Alkaline Phosphatase

Topics

• Alkaline Phosphatase (genetics)
• Asian People (genetics)
• Child, Preschool
• Female
• Genotype
• Humans
• Hypophosphatasia (enzymology, genetics)
• Infant
• Infant, Newborn
• Japan
• Male
• Mutation, Missense
• Phenotype
• Sequence Deletion