Abstract
The risk associated with the serum amyloid A (SAA) 1 gene and developing AA-amyloidosis is still controversial. In familial Mediterranean fever or Caucasoid rheumatoid arthritis (RA), the SAA1.1 allele is a risk factor for the development of AA-amyloidosis. However, individuals with the SAA1.3 allele are susceptible to AA-amyloidosis in the Japanese RA population, but those with the SAA1.1 are not. Previous reports have indicated that the − 13T/C single nucleotide polymorphism (SNP) at the 5’-flanking region of SAA1 appears to be a better marker of AA-amyloidosis than the exon-3 based haplotype, i.e., SAA1.1 or SAA1.3, in both Japanese and American Caucasian populations. So far, it is unknown why the − 13T SNP increases the amyloidogenicity of the patients. In the present study, a luciferase reporter gene assay showed that the transcriptional activity of the SAA1 having the − 13T-containing promoter was significantly higher than activities of those with − 13C-containing promoters (Fisher's protected least significance difference test). We suggest that having the − 13T SNP in the SAA1 promoter correlates with the amyloidogenicity in part as a result of this increased transcriptional activity.
RA, rheumatoid arthritis; FMF, familial Mediterranean fever; SAA, serum amyloid A; SNP, single nucleotide polymorphism; A-SAA, acute phase serum amyloid A
RA, rheumatoid arthritis; FMF, familial Mediterranean fever; SAA, serum amyloid A; SNP, single nucleotide polymorphism; A-SAA, acute phase serum amyloid A