National Changhua University of Education Institutional Repository : Item 987654321/11507
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 6507/11669
造訪人次 : 29717562      線上人數 : 402
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 進階搜尋

請使用永久網址來引用或連結此文件: http://ir.ncue.edu.tw/ir/handle/987654321/11507

題名: Skeletal Dysplasia Caused by FGFR3 Mutation in Taiwanese Patients
第三號纖母細胞成長因子受體基因突變引起的骨酪異化症
作者: Tsai, F. J.;Lee, C. C.;Wu, J. Y.;Yang, T. Y.;Wang, Nancy M.;Yang, C. F.;Peng, C. T.;Tsai, C. H.
貢獻者: 生物技術研究所
關鍵詞: Achondroplasia;Amplification created restriction site;ACRS;Fibroblast growth factor receptor3;FGFR3;Hypochondroplasia;Thanatophoric dysplasia
骨骼異化症;第三號纖母細胞成長因子受體基因
日期: 2000-03
上傳時間: 2012-06-06T02:04:05Z
出版者: 中臺灣醫學科學雜誌社
摘要: Background. The identification of a missense mutation (G380R) in the fibroblast growth factor receptor 3 (FGFR3) gene in patients with achondroplasia was followed by the detection of common FGFR3 mutations in two clinically related occurrences of skeletal dysplasia.: hypochondroplasia, and thanatophoric dysplasia. In this study, we investigated the FGFR3 mutation of achondroplasia, hypochondroplasia, and thanatophoric dysplasia in Taiwanese patients. Methods: There were 28 patients with achondroplasia, 18 with hypochondroplasia and two with thanatophoric dysplasia type I included in this study. Polymerase chain reaction (PCR), direct sequencing, and amplification created restriction site (ACRS) tests were performed to analyze the mutations on FGFR3 in these patients. Results: Genetic homogeneity of achondroplasia was demonstrated as recurrent G380R mutations in all patients hitherto reported. Although all detected mutations of hypochondroplasia were accounted for by a recurrent N540K mutation in the first tyrosine kinase domain of the receptor, a significant portion (45%) of our patients did not harbor the N540K mutation. Two patients with type I thanatophoric dysplasia were found to carry the R248C mutation. Conclusions: We used either a natural restriction enzyme site or ACRS to detect the recurrent G380R mutation of achondroplasia. The use of the ACRS was found to be more cost-effective and efficient than the use of the natural restriction enzyme digest.
背景 第三號纖母細胞成長因子受體(FG FR3)基因上的突變會導致骨骼異化症是最近分子生物學的最重要發現之一。為了解台灣這類型疾病上的基因突變情形我們分析了achondroplasia,hypochondroplasia及thanatophoric dysplasia的病人其FGFI好的特殊點突變。方法 利用聚合酶連鎖反應、基因定序以及酵素內切法,找出骨骼異化症的突變。結果 所有的achondroplasia病人都帶有G380R的突變,而在hypochondroplasia病人身上則具有一常見的N540K的突變,但仍有45%的病人不具此突變,另外兩名罕見的thanatophoric dysplasia病人都有R248C突變。結論 本研究證實利用ACRS的方法偵測achondroplasia比傳統的酵素內切法更其效力。
關聯: Mid-Taiwan Journal of Medicine, 5(1): 16-21
顯示於類別:[生物技術研究所] 期刊論文

文件中的檔案:

檔案 大小格式瀏覽次數
2020700310027.pdf53KbAdobe PDF1527檢視/開啟


在NCUEIR中所有的資料項目都受到原著作權保護.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋