Bobrowski Adam, Wojdyła Tomasz, Kimmel Marek
Department of Mathematics, Faculty of Electrical Engineering, Technical University of Lublin, 20-618 Lublin, Poland.
J Math Biol. 2010 Sep;61(3):455-73. doi: 10.1007/s00285-009-0308-1. Epub 2009 Nov 11.
In this paper, we extend the theoretical treatment of the Moran model of genetic drift with recombination and mutation, which was previously introduced by us for the case of two loci, to the case of n loci. Recombination, when considered in the Wright-Fisher model, makes it considerably less tractable. In the works of Griffiths, Hudson and Kaplan and their colleagues important properties were established using the coalescent approach. Other more recent approaches form a body of work to which we would like to contribute. The specific framework used in our paper allows finding close-form relationships, which however are limited to a set of distributions, which jointly characterize allelic states at a number of loci at the same or different chromosome(s) but which do not jointly characterize allelic states at a single locus on two or more chromosomes. However, the system is sufficiently rich to allow computing, albeit in general numerically, all possible multipoint linkage disequilibria under recombination, mutation and drift. We explore the algorithms enabling construction of the transition probability matrices of the Markov chain describing the process. We find that asymptotically the effects of recombination become indistinguishable, at least as characterized by the set of distributions we consider, from the effects of mutation and drift. Mathematically, the results are based on the foundations of the theory of semi-groups of operators. This approach allows generalization to any Markov-type mutation model. Based on these fundamental results, we explore the rates of convergence to the limit distribution, using Dobrushin's coefficient and spectral gap.
在本文中,我们将之前针对两个基因座情况引入的具有重组和突变的遗传漂变莫兰模型的理论处理扩展到了(n)个基因座的情况。在赖特 - 费希尔模型中考虑重组时,会使其处理起来变得相当棘手。在格里菲思、哈德森、卡普兰及其同事的工作中,使用合并方法确立了重要性质。其他一些更新的方法构成了一个我们希望有所贡献的工作体系。我们论文中使用的特定框架允许找到封闭形式的关系,然而这些关系仅限于一组分布,这些分布共同表征同一或不同染色体上多个基因座处的等位基因状态,但不能共同表征两条或更多条染色体上单个基因座处的等位基因状态。不过,该系统足够丰富,能够计算(尽管通常是数值计算)在重组、突变和漂变情况下所有可能的多点连锁不平衡。我们探索了能够构建描述该过程的马尔可夫链转移概率矩阵的算法。我们发现,渐近地,至少从我们所考虑的分布集的角度来看,重组的影响与突变和漂变的影响变得难以区分。从数学上讲,这些结果基于算子半群理论的基础。这种方法允许推广到任何马尔可夫型突变模型。基于这些基本结果,我们使用多布鲁申系数和谱隙来探索收敛到极限分布的速率。