| Project/Area Number |
15390633
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Orthodontic/Pediatric dentistry
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| Research Institution | Osaka University |
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Principal Investigator |
SHINTANI Seikou Osaka University, Graduate School of Dentistry, Associate Professor, 大学院・歯学研究科, 助教授 (90273698)
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| Co-Investigator(Kenkyū-buntansha) |
OOSHIMA Takashi Osaka University, Graduate School of Dentistry, Professor, 大学院・歯学研究科, 教授 (80116003)
TOYOSAWA Satoru Osaka University, Graduate School of Dentistry, Professor, 大学院・歯学研究科, 教授 (30243249)
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| Project Period (FY) |
2003 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥14,800,000 (Direct Cost: ¥14,800,000)
Fiscal Year 2004: ¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 2003: ¥10,800,000 (Direct Cost: ¥10,800,000)
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| Keywords | amelogenesis imperfecta / ameloblastin / enamelin / enamelysin / gene diagnosis / polymorphism / ポロモルフィズム / エナメリシン |
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| Research Abstract |
Amelogenesis imperfecta(AI) is a group of inherited disorders affecting enamel formation that are characterized by clinical and genetic heterogeneity. It is genetically classified into two forms, X-linked caused by the mutated amelogenin gene and autosomal. To date, only several types resulted from mutations of the gene encoding enamelin, kalliklein 4, enamelysin, and DLX3 although they are much more prevalent than X-linked form. We have recently cloned the human ameloblastin gene. Ameloblastin is one of the extracellular matrix proteins in tooth enamel and may be responsible for autosomal amelogenesis imperfecta(AI), since it plays a significant role in enamel crystal growth. Hence, the ameloblastin gene is also considered to be a candidate responsible for autosomal AI. We investigated polymorphisms of the human ameloblastin gene by polymerase chain reaction, DNA sequencing and single-strand conformational polymorphism(SSCP) analysis using genomic DNA from 50 Japanese subjects with sound dentition. One single sequential trinucleotide deletion and 3 single-nucleotide polymorphisms(SNPs) were identified in the translated region. The nucleotide deletion results in the lack of an amino acid residue and 2 of the SNPs cause nonsynonymous substitutions of amino acid residues. These results provide important background information for the investigation of autosomal AI in Japanese patients. Subsequently, we focussed our attention on the ameloblastin genes of 3 Japanese patients and also investigated the gene encoding enamelin and enamelysin. However, no pathogenic mutation in these genes of AI patients was detected. It was suggested that the exploration was extended to promoter regions of them, as well as coding regions of other expectant genes.
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