Stratil A, Cízová D, Hojný J, Hradecký J
Czechoslovak Academy of Sciences, Institute of Animal Physiology and Genetics, Department of Genetics, Libĕchov.
Anim Genet. 1990;21(3):267-76. doi: 10.1111/j.1365-2052.1990.tb03236.x.
Polymorphism of an alpha-protease inhibitor, PI3, in pig serum samples was detected using 2D agarose gel (pH 5.4)--polyacrylamide gel (pH 9.0) electrophoresis. Evidence was obtained that the five variants observed (A, B1, B2, C and D) are under genetic control by codominant alleles (Pi3A, Pi3B1, Pi3B2, Pi3C and Pi3D) at one autosomal locus. Variants A, B1, B2 and C inhibited chymotrypsin; there was no appreciable inhibition of trypsin and papain. Variant D did not inhibit chymotrypsin, and therefore its classification as a PI3 variant was put in question. PI3 typing was not possible in about 50% of the studied pigs since in those cases the PI3 variants were either too weak or absent. On the basis of backcross matings and haplotyping in complete families for protease inhibitor loci Pi1, Po1A, Pi2 and Pi3 it was proved that the Pi3 locus belongs to the protease inhibitor gene cluster, and the position of the locus in the linkage group was proposed as being Pi1-Po1A-(Po1B)-Pi3-Pi2-(Igh1, Igh2, Igh3, Igh4).
利用二维琼脂糖凝胶(pH 5.4)-聚丙烯酰胺凝胶(pH 9.0)电泳检测猪血清样本中α-蛋白酶抑制剂PI3的多态性。有证据表明,观察到的五个变体(A、B1、B2、C和D)受一个常染色体位点上的共显性等位基因(Pi3A、Pi3B1、Pi3B2、Pi3C和Pi3D)的遗传控制。变体A、B1、B2和C可抑制胰凝乳蛋白酶;对胰蛋白酶和木瓜蛋白酶没有明显抑制作用。变体D不抑制胰凝乳蛋白酶,因此其作为PI3变体的分类受到质疑。在约50%的受试猪中无法进行PI3分型,因为在这些情况下,PI3变体要么太弱,要么不存在。基于蛋白酶抑制剂基因座Pi1、Po1A、Pi2和Pi3的回交交配和完整家系的单倍型分析,证明Pi3基因座属于蛋白酶抑制剂基因簇,并提出该基因座在连锁群中的位置为Pi1-Po1A-(Po1B)-Pi3-Pi(2-Igh1、Igh2、Igh3、Igh4)。