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毛发-鼻-指综合征伴多生牙

Tricho-rhino-phalangeal syndrome with supernumerary teeth.

作者信息

Kantaputra P, Miletich I, Lüdecke H-J, Suzuki E Y, Praphanphoj V, Shivdasani R, Wuelling M, Vortkamp A, Napierala D, Sharpe P T

机构信息

Department of Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Thailand.

出版信息

J Dent Res. 2008 Nov;87(11):1027-31. doi: 10.1177/154405910808701102.

Abstract

Tricho-rhino-phalangeal syndromes (TRPS) are caused by mutation or deletion of TRPS1, a gene encoding a GATA transcription factor. These disorders are characterized by abnormalities of the hair, face, and selected bones. Rare cases of individuals with TRPS displaying supernumerary teeth have been reported, but none of these has been examined molecularly. We used two different approaches to investigate a possible role of TRPS1 during tooth development. We looked at the expression of Tprs1 during mouse tooth development and analyzed the craniofacial defects of Trps1 mutant mice. In parallel, we investigated whether a 17-year-old Thai boy with clinical features of TRPS and 5 supernumerary teeth had mutation in TRPS1. We report here that Trps1 is expressed during mouse tooth development, and that an individual with TRPS with supernumerary teeth has the amino acid substitution A919V in the GATA zinc finger of TRPS1. These results suggest a role for TRPS1 in tooth morphogenesis.

摘要

毛发-鼻-指(趾)综合征(TRPS)由TRPS1基因突变或缺失引起,TRPS1是一种编码GATA转录因子的基因。这些病症的特征是毛发、面部和特定骨骼出现异常。已有报道称,罕见的TRPS个体出现多生牙,但均未进行分子检测。我们采用两种不同方法研究TRPS1在牙齿发育过程中可能发挥的作用。我们观察了Tprs1在小鼠牙齿发育过程中的表达情况,并分析了Trps1突变小鼠的颅面缺陷。同时,我们调查了一名患有TRPS临床特征和5颗多生牙的17岁泰国男孩的TRPS1是否存在突变。我们在此报告,Trps1在小鼠牙齿发育过程中表达,并且一名患有TRPS和多生牙的个体在TRPS1的GATA锌指中有A919V氨基酸替换。这些结果表明TRPS1在牙齿形态发生中发挥作用。

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