The human serum amyloid A (SAA) gene family consists of two acute phas
e genes, SAA1 and SAA2; a pseudogene, SAA3 and a fourth gene, SAA4. Th
e existence of SAA4 was first described in this laboratory. Subsequent
ly, Sack and Talbot isolated a clone, designated GSAA4, which had homo
logy to SAA3. The clone was described as the same as SAA4 and was char
acterized as a pseudogene. However, our restriction site and sequence
analyses of SAA4 demonstrated that SAA4 and GSAA4 are separate entitie
s. SAA4 encodes a functional, constitutively expressed protein. Recent
ly, the GSAA4 clone has been reported by Sellar and Whitehead as const
ituting a fifth SAA-related sequence. However, we have demonstrated th
at GSAA4 has striking homology with the 3' terminus of SAA3 in the rev
erse orientation. Furthermore, computer analyses strongly indicate tha
t the GSAA4 or fifth SAA-related sequence is in fact, a clone from the
SAA3 locus. We have amplified, isolated and sequenced fragments from
genomic DNA which demonstrate that the GSAA4 sequence is the correct s
equence of the 3' region of SAA3. The SAA family must therefore still
be viewed as consisting of four SAA loci at present.