Two independent mutations in a family with neurofibromatosis type 1 (NF1)

✍ Scribed by Klose, Anja; Peters, Hartmut; Hoffmeyer, Sven; Buske, Annegret; L�der, Andrea; He�, Detlef; Lehmann, R�diger; N�rnberg, Peter; Tinschert, Sigrid

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 39 KB
• Volume: 83
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/(sici)1096-8628(19990305)83:1<6::aid-ajmg3>3.0.co;2-e

✦ Synopsis

We report on two independent alterations of the NF1 gene in a three-generation kindred with neurofibromatosis type 1 (NF1). Using temperature gradient gel electrophoresis (TGGE) in a mutation analysis of exon 31 of the NF1 gene we detected the previously reported nonsense mutation R1947X. This Cto-T transition at codon 1947 in exon 31 is considered to represent a mutation ''hot spot'' of the NF1 gene due to 5m CpG deamination. All living family members together with their genomic DNA were included in this investigation. However, the mutation R1947X was absent from two undoubtedly affected siblings of the propositus. Another NF1 mutation (889-2A→G) was identified in the two sibs by the protein truncation test (PTT). The novel splice site mutation 889-2A→G results in a skip of NF1 exon 7 during splicing and protein truncation due to frameshift. The two NF1 alterations are linked to different paternal haplotypes. In our study of a three-generation kindred, R1947X represents a de novo mutation whereas 889-2A→G is an inherited splice mutation. Implications for phenotype variation are discussed. Am. J. Med. Genet. 83: 6-12, 1999.