Hutchinson Sarah, Furger Andre, Halliday Dorothy, Judge Daniel P, Jefferson Andrew, Dietz Harry C, Firth Helen, Handford Penny A
Department of Biochemistry, University of Oxford, Oxford, UK.
Hum Mol Genet. 2003 Sep 15;12(18):2269-76. doi: 10.1093/hmg/ddg241. Epub 2003 Jul 22.
FBN1 mutations cause Marfan syndrome (MFS), an autosomal dominant disorder of connective tissue. One of the unexplained features of MFS is the pathogenic mechanism that leads to marked inter- and intra-familial clinical variability, despite complete disease penetrance. An FBN1 deletion patient [46,XXdel(15)(q15q22.1)] was identified whose fibrillin-1 protein and mRNA levels were significantly higher than expected for a single FBN1 allele. This suggested that allelic variation in normal FBN1 expression might occur in MFS families, and have potential clinical implications particularly for those with premature termination codon (PTC) mutations who usually display low levels of expression from the mutant allele due to nonsense-mediated decay (NMD). RNA analyses identified a variable reduction in total FBN1 transcript (78+/-2.2 to 27.3+/-2.3%) in three related individuals carrying PTC-causing mutation 932insT, compared with unaffected control individuals. Both pulse chase analysis of fibrillin-1 biosynthesis and RNase protection analyses demonstrated that these differences were due to variation in the expression of the normal FBN1 allele and not NMD of mutant RNA. We suggest that differences in normal FBN1 expression could contribute to the clinical variability seen in this family with MFS, and should be considered as a potential modifier of phenotype in other cases of MFS.
FBN1基因突变导致马凡综合征(MFS),这是一种常染色体显性结缔组织疾病。MFS一个无法解释的特征是,尽管疾病完全外显,但导致显著的家族间和家族内临床变异性的致病机制。鉴定出一名FBN1缺失患者[46,XXdel(15)(q15q22.1)],其原纤蛋白-1蛋白和mRNA水平显著高于单个FBN1等位基因预期的水平。这表明正常FBN1表达中的等位基因变异可能在MFS家族中发生,并且具有潜在的临床意义,特别是对于那些具有过早终止密码子(PTC)突变的患者,由于无义介导的衰变(NMD),这些患者通常突变等位基因的表达水平较低。RNA分析发现,与未受影响的对照个体相比,三名携带导致PTC突变932insT的相关个体中,FBN1转录本总量有不同程度的减少(78±2.2%至27.3±2.3%)。对原纤蛋白-生物合成的脉冲追踪分析和核糖核酸酶保护分析均表明,这些差异是由于正常FBN1等位基因表达的变化,而非突变RNA的NMD。我们认为,正常FBN1表达的差异可能导致该MFS家族中出现的临床变异性,并且在其他MFS病例中应被视为潜在的表型修饰因素。