| Project/Area Number |
02670467
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Pediatrics
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| Research Institution | Department of Pediatrics & Child Health, Kurume University School of Medicine |
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Principal Investigator |
YOSHINO Makoto Kurume University School of Medicine, Associate Professor, 医学部, 助教授 (40080569)
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| Co-Investigator(Kenkyū-buntansha) |
NAKAO Mitsuyoshi Kurume University School of Medicine, Research Associate, 医学部, 助手 (00217663)
NISHIYORI Atsushi Kurume University School of Medicine, Research Associate, 医学部, 助手 (30218226)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1991: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1990: ¥1,000,000 (Direct Cost: ¥1,000,000)
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| Keywords | Phenylketonuria / Phenylalanine hydroxylase / Mutation / Japanese population / フェニ-ルアラニン代謝異常 / 遺伝子 / 変異 |
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| Research Abstract |
Objectives : At least thirty-one mutations at the phenylalanine hydroxylase gene locus have been identified among various ethnic populations. Significant differences in the distribution of such mutations are known among such ethnic populations. This project was designed to elucidate mutations at the phenylalanine hydroxylase gene among the Japanese phenylketonuric and hyperphenylalaninemic patients.
Materials and Methods : Three phenylketonurics, one hyperphenylalaninemic patient and two healthy individuals were enrolled in this study. Genomic DNA was extracted from peripheral leukocytes or lymphocytes after proteinase K digestion by phenol extraction. Exons 3 and 5 of the phenylalanine hydroxylase gene were amplified by the polymerase chain reaction technique with the DNA specimens extracted from these individuals as templates. Sequences of primers were as previously described. The amplified exons were cloned and subjected to sequencing by a dideoxy technique.
Results : A ^<553>C->T mutation (R111Ter mutation) was found in one allele of one of the phenylketonurics. The mutations at the other allele of this patient and in the other patients have not been identified.
Comments : This mutation have been identified among the Chinese phenylketonuric patients, and accordingly is of etiological significance. Analysis of mutations in the other allele of this patient and in the other patient are now in progress.
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