Yoshida A, Davé V, Branch D R, Yamaguchi H, Okubo Y
Am J Hum Genet. 1982 Nov;34(6):919-24.
The blood type A is known to be subclassified as A1, A2, and A1-A2 intermediate (Aint), depending upon red cell agglutinability with anti-A1 and anti-H lectins. Approximately 80% of the blood group H-sites remained unglycosylated in type Aint erythrocyte membranes. Plasma from Aint individuals contains a special blood group GalNAc transferase (UDP-GalNAc:2'-fucosylgalactoside-alpha-3-N-acetylgalactosaminyl transferase), which is different from the enzyme in A1 plasma and the enzyme in A2 plasma. A1-enzyme has strong affinity to UDP-GalNAc and 2'-fucosyllactose, A2-enzyme has low affinity to both substrates, and Aint-enzyme has strong affinity to UDP-GalNAc and very low affinity to 2'-fucosyllactose, which is a soluble analog of the H-substances. The low degree of glycosylation of the blood group H-sites due to the low affinity of Aint-enzyme with the H-substances can account for the lower A activity and higher H activity in Aint red cells than in A1 red cells. The blood group A allele can be subdivided into three common alleles, A1, A2, and Aint, each controlling the formation of different types of blood group GalNAc transferases.
已知血型A可根据红细胞与抗A1和抗H凝集素的凝集性分为A1、A2和A1 - A2中间型(Aint)。在Aint型红细胞膜中,约80%的血型H位点未被糖基化。Aint个体的血浆中含有一种特殊的血型N - 乙酰半乳糖胺转移酶(UDP - GalNAc:2'-岩藻糖基半乳糖-α-3-N-乙酰半乳糖胺转移酶),它与A1血浆中的酶和A2血浆中的酶不同。A1酶对UDP - GalNAc和2'-岩藻糖基乳糖有很强的亲和力,A2酶对这两种底物的亲和力较低,而Aint酶对UDP - GalNAc有很强的亲和力,对2'-岩藻糖基乳糖(H物质的可溶性类似物)的亲和力非常低。由于Aint酶与H物质的亲和力低,导致血型H位点的糖基化程度低,这可以解释Aint红细胞中A活性低于A1红细胞且H活性高于A1红细胞的现象。血型A等位基因可细分为三个常见等位基因,A1、A2和Aint,每个等位基因控制不同类型血型N - 乙酰半乳糖胺转移酶的形成。