Kluve-Beckerman B, Long G L, Benson M D
Biochem Genet. 1986 Dec;24(11-12):795-803. doi: 10.1007/BF00554519.
Serum amyloid A (SAA) is an acute-phase reactant and precursor to amyloid A protein, the major constituent of the fibril deposits of reactive amyloidosis. The factors determining whether the 104-amino acid SAA molecule is converted into the 76-amino acid amyloid A protein and deposited as fibrils are not known. As an initial step toward investigating the possibility that a particular primary structure of SAA is involved in amyloid formation, we have cloned and determined the nucleotide sequence of human SAA-specific cDNAs. The first clone, selected using an oligonucleotide probe, was shown to encode the signal peptide and amino-terminal region of SAA. The cDNA of this clone served as probe in the selection of two distinct, full-length SAA cDNAs, initially differentiated by the presence (pSAA21) or absence (pSAA82) of a PstI site in the coding sequence. The complete nucleotide sequence of pSAA82 cDNA was determined. Since there appear to be multiple human SAA alleles, it is conceivable that their differential expression is important to amyloid formation.
血清淀粉样蛋白A(SAA)是一种急性期反应物,也是淀粉样蛋白A的前体,而淀粉样蛋白A是反应性淀粉样变性原纤维沉积物的主要成分。决定104个氨基酸的SAA分子是否会转化为76个氨基酸的淀粉样蛋白A并以原纤维形式沉积的因素尚不清楚。作为研究SAA的特定一级结构是否参与淀粉样蛋白形成可能性的第一步,我们克隆并确定了人SAA特异性cDNA的核苷酸序列。使用寡核苷酸探针选择的第一个克隆被证明编码SAA的信号肽和氨基末端区域。该克隆的cDNA在选择两个不同的全长SAA cDNA时用作探针,最初这两个cDNA根据编码序列中PstI位点的存在(pSAA21)或不存在(pSAA82)来区分。确定了pSAA82 cDNA的完整核苷酸序列。由于似乎存在多个人类SAA等位基因,可以想象它们的差异表达对淀粉样蛋白形成很重要。