Relaxing the Hypotheses of Symmetry and Time-Reversibility in Genome Evolutionary Models

J. Bahi, C. Guyeux, A. Perasso
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引用次数: 1

Abstract

Various genome evolutionary models have been proposed these last decades to predict the evolution of a DNA sequence over time, essentially described using a mutation matrix. By essence, all of these models relate the evolution of DNA sequences to the computation of the successive powers of the mutation matrix. To make this computation possible, hypotheses are assumed for the matrix, such as symmetry and time-reversibility, which are not compatible with mutation rates that have been recently obtained experimentally on genes ura3 and can1 of the Yeast Saccharomyces cerevisiae. In this work, authors investigate systematically the possibility to relax either the symmetry or the time-reversibility hypothesis of the mutation matrix, by investigating all the possible matrices of size 2*2 and 3*3. As an application example, the experimental study on the Yeast Saccharomyces cerevisiae has been used in order to deduce a simple mutation matrix, and to compute the future evolution of the rate purine/pyrimidine for $ura3$ on the one hand, and of the particular behavior of cytosines and thymines compared to purines on the other hand.
放宽基因组进化模型中的对称性和时间可逆性假设
在过去的几十年里,已经提出了各种基因组进化模型来预测DNA序列随时间的进化,基本上是用突变矩阵来描述的。从本质上讲,所有这些模型都将DNA序列的进化与突变矩阵的连续幂的计算联系起来。为了使计算成为可能,对矩阵进行了假设,例如对称性和时间可逆性,这些假设与最近在酵母的ura3和can1基因上实验获得的突变率不相容。在本文中,作者通过研究大小为2*2和3*3的所有可能矩阵,系统地研究了突变矩阵的对称性或时间可逆性假设松弛的可能性。作为一个应用实例,本文通过对酵母(Saccharomyces cerevisiae)的实验研究,一方面推导了一个简单的突变矩阵,一方面计算了$ura3$的嘌呤/嘧啶比率的未来演变,另一方面计算了胞嘧啶和胸腺嘧啶相对于嘌呤的特殊行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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