The c-FOS gene product, a putative transacting transcriptional regulator of the amyloid precursor protein (APP) gene, is a candidate locus for the familial Alzheimer's disease (FAD) mutation on chromosome 14 (FAD14). In light of this functional relationship, we investigated the nucleotide sequence and segregation of c-FOS and the nucleotide sequence of the 5' APP promoter. Single-stranded conformational polymorphisms (SSCPs) in the c-FOS gene revealed that c-FOS closely cosegregates with the FAD14 gene but does not show allelic association with FAD. A conservative third-position T→C mutation was demonstrated in exon 2 (codon 84) of c-FOS, and a C→G substitution was detected at—209 bp in the 5' promoter of APP. Neither were unique to FAD and are unlikely to be pathogenic or secondary modifiers of the FAD phenotype. We conclude that the c-FOS open reading frame is probably not the site of the FAD14 locus, but we cannot exclude the existence of modifier loci on chromosome 21. © 1993 American Academy of Neurology.
Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial alzheimer's disease / Rogaev E.I.; Lukiw W.J.; Vaula G.; Haines J.L.; Rogaeva E.A.; Tsuda T.; Alexandrova N.; Liang Y.; Mortilla M.; Amaducci L.; Bergamini L.; Bruni A.C.; Foncin J.-F.; Macciardi F.; Montesi M.P.; Sorbi S.; Rainero I.; Pinessi L.; Polinsky R.J.; Frommelt P.; Duara R.; Lopez R.; Pollen D.; Gusella J.F.; Tanzi R.; Maclachlan D.C.; St. George-Hyslop P.H.. - In: NEUROLOGY. - ISSN 0028-3878. - STAMPA. - 43:(1993), pp. 2275-2279. [10.1212/wnl.43.11.2275]
Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial alzheimer's disease
Mortilla M.;Amaducci L.;Macciardi F.;Sorbi S.;
1993
Abstract
The c-FOS gene product, a putative transacting transcriptional regulator of the amyloid precursor protein (APP) gene, is a candidate locus for the familial Alzheimer's disease (FAD) mutation on chromosome 14 (FAD14). In light of this functional relationship, we investigated the nucleotide sequence and segregation of c-FOS and the nucleotide sequence of the 5' APP promoter. Single-stranded conformational polymorphisms (SSCPs) in the c-FOS gene revealed that c-FOS closely cosegregates with the FAD14 gene but does not show allelic association with FAD. A conservative third-position T→C mutation was demonstrated in exon 2 (codon 84) of c-FOS, and a C→G substitution was detected at—209 bp in the 5' promoter of APP. Neither were unique to FAD and are unlikely to be pathogenic or secondary modifiers of the FAD phenotype. We conclude that the c-FOS open reading frame is probably not the site of the FAD14 locus, but we cannot exclude the existence of modifier loci on chromosome 21. © 1993 American Academy of Neurology.
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