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马凡综合征的产前诊断:绒毛取样中纤连蛋白-1突变的鉴定。

Prenatal diagnosis of Marfan syndrome: identification of a fibrillin-1 mutation in chorionic villus sample.

作者信息

Rantamäki T, Raghunath M, Karttunen L, Lönnqvist L, Child A, Peltonen L

机构信息

Department of Human Molecular Genetics, National Public Health Institute, Helsinki, Finland.

出版信息

Prenat Diagn. 1995 Dec;15(12):1176-81. doi: 10.1002/pd.1970151217.

Abstract

Marfan syndrome (MFS) is one of the most common heritable connective tissue disorders and is caused by mutations in a gene coding for fibrillin-1. All but one of over 30 published mutations have been unique and specific prenatal diagnostics can only be provided to families with a previously established mutation. We have earlier identified a 366 bp deletion of fibrillin mRNA in a three-generation British Marfan family. An affected female in the family together with her husband sought prenatal diagnosis. Chorionic villus sampling was performed at 11.5 weeks of gestation and total RNA was directly extracted from the sample. After reverse transcription and polymerase chain reaction (PCR) of the cDNA, the same deletion was identified in the chorionic villus sample (CVS) and the mother's sample in agarose gel electrophoresis. The fetal origin of the CVS was confirmed with polymorphic markers. In addition to the mutation analysis, CVS cells of the proband and a control fetus were cultured for biochemical studies of fibrillin polypeptides. The results of the biochemical investigation were in concordance with the molecular analysis.

摘要

马凡综合征(MFS)是最常见的遗传性结缔组织疾病之一,由编码原纤维蛋白-1的基因突变引起。已发表的30多种突变中,除一种外均为独特突变,只有之前已确定突变的家庭才能进行特定的产前诊断。我们之前在一个三代英国家庭中发现了原纤维蛋白mRNA的366 bp缺失。该家庭中一名受影响的女性与其丈夫寻求产前诊断。在妊娠11.5周时进行绒毛取样,并直接从样本中提取总RNA。对cDNA进行逆转录和聚合酶链反应(PCR)后,在琼脂糖凝胶电泳中,绒毛取样样本(CVS)和母亲样本中均鉴定出相同的缺失。通过多态性标记证实了CVS的胎儿来源。除了突变分析外,还对先证者和对照胎儿的CVS细胞进行培养,用于原纤维蛋白多肽的生化研究。生化研究结果与分子分析结果一致。

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