Azen E A, Hurley C K, Denniston C
Biochem Genet. 1979 Apr;17(3-4):257-79. doi: 10.1007/BF00498967.
Genetic polymorphism of the major glycoprotein (Gl) found in parotid saliva is determined by autosomal inheritance of one unexpressed and four expressed alleles. This hypothesis is supported by studies in 41 white families including 146 children. For 143 randomly collected salivas from whites and 82 randomly collected salivas from blacks, maximum likelihood estimates of the gene frequencies are as follows: for whites, Gl1 = 0.742, Gl2 = 0.040, Gl3 = 0.155, Gl4 = 0.017, Gl0 = 0.46; for blacks, Gl1 = 0.459, Gl2 = 0.050, Gl3 = 0.337, Gl4 = 0.044, Gl0 = 0.110. There is strong evidence for linkage of Gl/Pr (seven families, lod score at theta = 0 is 5.24) and G1/Db (eight families, lod score at theta = 0 is 4.45). The allelic products of Gl show evidence for linkage disequilibrium with the products of the Pr, Db, and Pa loci (P less than 0.0005). On the basis of varying degrees of linkage disequilibrium, Gl may be closer to Db than to Pr or Pa and on the "outside" of Db with respect to Pr or Pa. Amino acid analyses of Gl 1 and Gl 4 proteins show strong resemblances in composition to the major basic glycoprotein and the acidic proline-rich proteins of parotid saliva described by other workers. The polymorphic forms of the Gl proteins show microheterogeneity due to variability in charge and molecular weight. The electrophoretic polymorphism appears to be determined by apparent differences in molecular weights between the Gl proteins.
腮腺唾液中主要糖蛋白(Gl)的遗传多态性由一个未表达等位基因和四个表达等位基因的常染色体遗传决定。这一假设得到了对41个白人家庭(包括146名儿童)的研究支持。对于随机收集的143份白人唾液和82份黑人唾液,基因频率的最大似然估计如下:白人中,Gl1 = 0.742,Gl2 = 0.040,Gl3 = 0.155,Gl4 = 0.017,Gl0 = 0.46;黑人中,Gl1 = 0.459,Gl2 = 0.050,Gl3 = 0.337,Gl4 = 0.044,Gl0 = 0.110。有强有力的证据表明Gl/Pr(7个家庭,θ = 0时的连锁值为5.24)和G1/Db(8个家庭,θ = 0时的连锁值为4.45)存在连锁。Gl的等位基因产物显示出与Pr、Db和Pa位点的产物存在连锁不平衡的证据(P小于0.0005)。基于不同程度的连锁不平衡,相对于Pr或Pa,Gl可能比Pr或Pa更靠近Db,且在Db相对于Pr或Pa的“外侧”。对Gl 1和Gl 4蛋白的氨基酸分析表明,其组成与其他研究者描述的腮腺唾液中的主要碱性糖蛋白和富含酸性脯氨酸的蛋白有很强的相似性。Gl蛋白的多态形式由于电荷和分子量的变化而表现出微异质性。电泳多态性似乎由Gl蛋白之间分子量的明显差异决定。