Liu Tian, Todhunter Rory J, Lu Qing, Schoettinger Lindsay, Li Hongying, Littell Ramon C, Burton-Wurster Nancy, Acland Gregory M, Lust George, Wu Rongling
Department of Statistics, University of Florida, Gainesville, Florida 32611, USA.
Genetics. 2006 Sep;174(1):439-53. doi: 10.1534/genetics.106.060137. Epub 2006 Jul 18.
Unlike gametic linkage disequilibrium defined for a random-mating population, zygotic disequilibrium describes the nonrandom association between different loci in a nonequilibrium population that deviates from Hardy-Weinberg equilibrium. Zygotic disequilibrium specifies five different types of disequilibria simultaneously that are (1) Hardy-Weinberg disequilibria at each locus, (2) gametic disequilibrium (including two alleles in the same gamete, each from a different locus), (3) nongametic disequilibrium (including two alleles in different gametes, each from a different locus), (4) trigenic disequilibrium (including a zygote at one locus and an allele at the other), and (5) quadrigenic disequilibrium (including two zygotes each from a different locus). However, because of the uncertainty on the phase of the double heterozygote, gametic and nongametic disequilibria need to be combined into a composite digenic disequilibrium and further define a composite quadrigenic disequilibrium together with the quadrigenic disequilibrium. To investigate the extent and distribution of zygotic disequilibrium across the canine genome, a total of 148 dogs were genotyped at 247 microsatellite markers located on 39 pairs of chromosomes for an outbred multigenerational pedigree, initiated with a limited number of unrelated founders. A major portion of zygotic disequilibrium was contributed by the composite digenic and quadrigenic disequilibrium whose values and numbers of significant marker pairs are both greater than those of trigenic disequilibrium. All types of disequilibrium are extensive in the canine genome, although their values tend to decrease with extended map distances, but with a greater slope for trigenic disequilibrium than for the other types of disequilibrium. Considerable variation in the pattern of disequilibrium reduction was observed among different chromosomes. The results from this study provide scientific guidance about the determination of the number of markers used for whole-genome association studies.
与针对随机交配群体定义的配子连锁不平衡不同,合子不平衡描述的是偏离哈迪 - 温伯格平衡的非平衡群体中不同基因座之间的非随机关联。合子不平衡同时指定了五种不同类型的不平衡,即(1)每个基因座处的哈迪 - 温伯格不平衡,(2)配子不平衡(包括同一配子中的两个等位基因,每个来自不同基因座),(3)非配子不平衡(包括不同配子中的两个等位基因,每个来自不同基因座),(4)三基因不平衡(包括一个基因座处的一个合子和另一个基因座处的一个等位基因),以及(5)四基因不平衡(包括来自不同基因座的两个合子)。然而,由于双杂合子相位的不确定性,配子不平衡和非配子不平衡需要合并为一个复合双基因不平衡,并与四基因不平衡一起进一步定义一个复合四基因不平衡。为了研究合子不平衡在犬类基因组中的程度和分布,对一个由有限数量的无关奠基者起始的远交多代家系中的148只狗,在位于39对染色体上的247个微卫星标记处进行了基因分型。合子不平衡的主要部分由复合双基因和四基因不平衡贡献,其显著标记对的值和数量均大于三基因不平衡。尽管所有类型的不平衡值往往会随着图谱距离的增加而降低,但三基因不平衡的斜率比其他类型的不平衡更大,不过所有类型的不平衡在犬类基因组中都很广泛。在不同染色体之间观察到不平衡减少模式存在相当大的差异。本研究结果为全基因组关联研究中使用的标记数量的确定提供了科学指导。