Singh Krishna Kumar, Shukla Praphulla Chandra, Rommel Kathrin, Schmidtke Jörg, Arslan-Kirchner Mine
Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
Eur J Hum Genet. 2006 Jul;14(7):876-9. doi: 10.1038/sj.ejhg.5201620. Epub 2006 Apr 12.
Marfan syndrome (MFS; OMIM#154700) is a connective tissue disorder characterized by manifestations in the ocular, skeletal and cardiovascular systems. MFS is caused by mutation in the fibrillin-1 gene (FBN1; OMIM#134797) and more than 550 mutations have been identified so far. FBN1 is approximately 230 kb in size and contains three evolutionarily conserved alternatively spliced exons B, A and C at the 5'end. In a first systematic attempt to associate sequence variations in the FBN1 5' alternatively spliced exons with MFS, we investigated 41 individuals fulfilling the diagnostic criteria of Ghent nosology or with features of MFS including at least one major criterion or involvement of two organ systems but not fulfilling a strict interpretation of the Ghent nosology, and known to be negative for mutations in the FBN1 exons 1-65 as well as the TGFBR2 and TGFBR1 coding regions. We identified five novel and one previously reported variants in the six unrelated probands and provide preliminary evidence for their role in pathogenesis.
马凡综合征(MFS;OMIM#154700)是一种结缔组织疾病,其特征表现于眼、骨骼和心血管系统。MFS由原纤蛋白-1基因(FBN1;OMIM#134797)突变引起,迄今为止已鉴定出550多种突变。FBN1大小约为230 kb,在5'端包含三个进化保守的可变剪接外显子B、A和C。在首次将FBN1 5'可变剪接外显子中的序列变异与MFS相关联的系统研究中,我们调查了41名符合根特分类法诊断标准或具有MFS特征(包括至少一项主要标准或两个器官系统受累,但不符合根特分类法的严格定义)的个体,且已知这些个体FBN1外显子1 - 65以及TGFBR2和TGFBR1编码区域的突变检测为阴性。我们在6名无关先证者中鉴定出5个新的和1个先前报道的变异,并为它们在发病机制中的作用提供了初步证据。