ID 83489
Author
Chen, Shuli Department of Pediatrics, The University of Tokushima School of Medicine
Ito, Michinori Department of Pediatrics, The University of Tokushima School of Medicine
Saijo, Takahiko Department of Pediatrics, The University of Tokushima School of Medicine
Naito, Etsuo Department of Pediatrics, The University of Tokushima School of Medicine
Kuroda, Yasuhiro Department of Pediatrics, The University of Tokushima School of Medicine Tokushima University Educator and Researcher Directory
Keywords
cystathionineβ-Synthase Deficiency
homocystinuria
mutation analysis
neonatal mass screening
Content Type
Journal Article
Description
Two mutations in the cystathionine β-synthase (CBS) gene were found in two Japanese siblings with pyridoxine non-responsive homocystinuria who had different methionine levels in their blood during the neonatal period. Both patients were com-pound heterozygotes of two mutant alleles:one had an A-to-G transition at nucleotide194 (A194G) that caused a histidine-to-arginine substitution at position 65 of the protein (H65R), while the other had a G-to-A transition at nucleotide346 (G346A) which resulted in a glycine-to-arginine substitution at position 116 of the protein (G116R). The two mutant proteins were separately expressed in Escherichia coli, and they completely lacked catalytic activity.
Despite their identical genotypes and almost equal protein intake, these siblings showed different levels of blood methionine during the neonatal period, suggesting that the level of methionine in blood is determined not only by the defect in the CBS gene and protein intake, but also by the activity of other enzymes involved in methionine and homocysteine metabolism, especially during the neonatal period. Therefore, high-risk newborns who have siblings with homocystinuria, even if the level of methionine in their blood is normal in a neonatal mass screening, should be followed up and diagnosed by an assay of enzyme activity or a gene analysis so that treatment can be begun as soon as possible to prevent the development of clinical symptoms. In addition, a new, more sensi-tive method for the mass screening of CBS deficiency in neonates should be developed.
Journal Title
The journal of medical investigation : JMI
ISSN
13431420
NCID
AA11166929
Volume
46
Issue
3-4
Start Page
186
End Page
191
Sort Key
186
Published Date
1999
Remark
FullText File
language
eng
departments
Medical Sciences