Faucz F R, Probst C M, Petzl-Erler M L
Laboratory of Human Molecular Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil.
Eur J Immunogenet. 2000 Feb;27(1):5-16. doi: 10.1046/j.1365-2370.2000.00186.x.
In the class II region of the major histocompatibility complex (MHC), four genes implicated in processing of MHC class I-presented antigens have been described. Two of these (TAP1 and TAP2) code for endoplasmic reticulum membrane transporter proteins and the other two (LMP2 and LMP7) for proteasome subunits. These genes are polymorphic, although much less so than classical MHC class I and II genes. There is controversy concerning the possible functional implications of this variation. Population genetics is one of the means of investigating the evolutionary and functional significance of genetic polymorphisms; however, few populations have been analysed with respect to TAP and LMP diversity. We present here the polymorphism of TAP1, TAP2, LMP2 and LMP7 genes in the Kaingang and Guarani Amerindian tribes, and in the Caucasoid population of the Brazilian State of Paraná. Allele frequencies found in the Caucasoids were close to those described for similar populations. Amerindians had a somewhat more restricted polymorphism, and allele and haplotype frequencies differed greatly between the two tribes. Overall linkage disequilibrium (LD) between the four genes was low in the Caucasoids, but high in the Amerindians, for which significant LD was seen for all informative pairs of loci. Comparing results of this and previous studies we observed that, whenever significant LD occurs in non-Amerindians, it tends to be similar in the different ethnic groups. While this might be interpreted as evidence of co-evolution of genes in the TAP-LMP region, the high haplotypic diversity in all populations and low LD in non-Amerindians indicate absence of co-evolution of the different genes. Distributions of allele and genotype frequencies are consistent with the hypothesis of selective neutrality. We conclude that genetic polymorphism of the human TAP and LMP genes and haplotypes is of little, if any, functional significance.
在主要组织相容性复合体(MHC)的II类区域,已描述了四个与MHC I类呈递抗原加工相关的基因。其中两个基因(TAP1和TAP2)编码内质网膜转运蛋白,另外两个基因(LMP2和LMP7)编码蛋白酶体亚基。这些基因具有多态性,尽管其多态性程度远低于经典的MHC I类和II类基因。关于这种变异可能的功能影响存在争议。群体遗传学是研究遗传多态性的进化和功能意义的方法之一;然而,针对TAP和LMP多样性进行分析的人群很少。我们在此展示了TAP1、TAP2、LMP2和LMP7基因在凯冈和瓜拉尼美洲印第安部落以及巴西巴拉那州高加索人群中的多态性。在高加索人群中发现的等位基因频率与类似人群中描述的频率相近。美洲印第安人的多态性在某种程度上更为受限,并且两个部落之间的等位基因和单倍型频率差异很大。在高加索人群中,这四个基因之间的总体连锁不平衡(LD)较低,但在美洲印第安人中较高,对于所有信息性位点对都观察到了显著的LD。比较本研究和先前研究的结果,我们观察到,每当在非美洲印第安人中出现显著的LD时,不同种族群体中的情况往往相似。虽然这可能被解释为TAP - LMP区域中基因共同进化的证据,但所有人群中高单倍型多样性以及非美洲印第安人中低LD表明不同基因不存在共同进化。等位基因和基因型频率的分布与选择中性假说一致。我们得出结论,人类TAP和LMP基因及单倍型的遗传多态性即使有功能意义也很小。