C to T transition at the first nucleotide of codon 63 of the beta-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy.

Abstract

Hemoglobin (Hb) M-Saskatoon, a beta variant of methemoglobin, is characterized by mild hemolysis. It is caused by the substitution of a histidine by a tyrosine at the 63rd amino acid residue of the beta-globin chain. Amplification and sequence analysis of genomic beta-globin DNA from an Indonesian boy diagnosed as having the more severe disease thalassemia demonstrated the presence of a C to T transition at nucleotide 473 in one of the two beta-globin genes resulting in a histidine to tyrosine substitution at 63rd residue. This amino acid change matched with that reported in Hb M-Saskatoon. This nucleotide change abolished a recognition site for the restriction endonuclease NlaIII. NlaIII digestion of the corresponding beta-globin DNA amplified from the patient's parents indicated that the mutation was inherited through from his mother. This result shows that the world-wide distribution of Hb M-Saskatoon extends to Indonesia, where it was not previously identified. Possible causes of the unusually severe symptoms observed in the case are discussed.

• Authors: P Suryantoro, Y Takeshima, A Haryanto, M Matsuo
• Journal: The Japanese journal of human genetics (Jpn J Hum Genet) Vol. 40 Issue 2 Pg. 195-201 (Jun 1995) ISSN: 0916-8478 [Print] Japan
• PMID: 7663000 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Codon
• Hemoglobins, Abnormal
• Nucleotides
• hemoglobin Saskatoon
• Globins

Topics

• Base Sequence
• Child
• Codon
• Globins (genetics)
• Hemoglobins, Abnormal (genetics)
• Humans
• Indonesia
• Male
• Molecular Sequence Data
• Nucleotides (genetics)
• Point Mutation
• beta-Thalassemia (genetics)