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PMID: 10782929 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Molecular analysis of the 5'-flanking region of the neurofibromatosis type 1 (NF1) gene: identification of five sequence variants.

Clinical genetics ·Vol. 57 ·No. 3 ·2000-03-00 ·页码 221-4

Osborn M, Cooper DN, Upadhyaya M

Abstract

Dideoxy fingerprinting was used to analyse the 5' flanking region of the neurofibromin (NF1) gene in a panel of 380 neurofibromatosis type 1 (NF1) patients. Five polymorphisms/rare variants were identified at positions -412, - 402, + 16, + 25 and + 132, but control data indicated that these were unlikely to be of pathological significance. Promoter mutations in the NF1 gene are not, therefore, a common cause of NF1. This notwithstanding, a reporter gene assay was performed to determine if these variants could affect the expression of the NF1 gene, and all three changes in the 5'-untranslated region (UTR) (+ 16, + 25, + 132) were found to be associated with a 60-70% increase in reporter gene expression.

MeSH 主题词
DNA Fingerprinting DNA Mutational Analysis Genes, Neurofibromatosis 1/genetics HeLa Cells Humans Luciferases/metabolism Neurofibromatosis 1/genetics Plasmids Polymerase Chain Reaction Polymorphism, Genetic Promoter Regions, Genetic Transfection
化学物质
Luciferases
作者与单位
共 3 位作者,点击展开单位 / ORCID
Osborn M
Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff, UK.
Cooper D N
Upadhyaya M
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
2000-03-00
页码
221-4
Language
English
Country/Region
Denmark
NLM ID
0253664
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