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串联阵列的持久性:对卫星DNA和简单序列DNA的影响

Persistence of tandem arrays: implications for satellite and simple-sequence DNAs.

作者信息

Walsh J B

出版信息

Genetics. 1987 Mar;115(3):553-67. doi: 10.1093/genetics/115.3.553.

DOI:10.1093/genetics/115.3.553
PMID:3569882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1216357/
Abstract

Recombination processes acting on tandem arrays are suggested here to have probable intrinsic biases, producing an expected net decrease in array size following each event, in contrast to previous models which assume no net change in array size. We examine the implications of this by modeling copy number dynamics in a tandem array under the joint interactions of sister-strand unequal crossing over (rate gamma per generation per copy) and intrastrand recombination resulting in deletion (rate epsilon per generation per copy). Assuming no gene amplification or selection, the expected mean persistence time of an array starting with z excess copies (i.e., array size z + 1) is z(1 + gamma/epsilon) recombinational events. Nontrivial equilibrium distributions of array sizes exist when gene amplification or certain forms of selection are considered. We characterize the equilibrium distribution for both a simple model of gene amplification and under the assumption that selection imposes a minimal array size, n. For the latter case, n + 1/alpha is an upper bound for mean array size under fairly general conditions, where alpha(= 2 epsilon/gamma) is the scaled deletion rate. Further, the distribution of excess copies over n is bounded above by a geometric distribution with parameter alpha/(1 + alpha). Tandem arrays are unlikely to be greatly expanded by unequal crossing over unless alpha much less than 1, implying that other mechanisms, such as gene amplification, are likely important in the evolution of large arrays. Thus unequal crossing over, by itself, is likely insufficient to account for satellite DNA.

摘要

本文提出作用于串联阵列的重组过程可能存在内在偏差,与先前假设阵列大小无净变化的模型相反,每次事件后阵列大小预计会出现净减少。我们通过对串联阵列中的拷贝数动态进行建模来研究其影响,该模型考虑了姐妹染色单体不等交换(每代每份拷贝的速率为γ)和导致缺失的链内重组(每代每份拷贝的速率为ε)的联合相互作用。假设没有基因扩增或选择,从z个额外拷贝开始(即阵列大小为z + 1)的阵列的预期平均持续时间为z(1 + γ/ε)次重组事件。当考虑基因扩增或某些形式的选择时,存在非平凡的阵列大小平衡分布。我们对基因扩增的简单模型以及选择施加最小阵列大小n的假设下的平衡分布进行了表征。对于后一种情况,在相当一般的条件下,n + 1/α是平均阵列大小的上限,其中α(= 2ε/γ)是缩放后的缺失率。此外,超过n的额外拷贝的分布以上界为参数为α/(1 + α)的几何分布。除非α远小于1,否则串联阵列不太可能通过不等交换而大幅扩展,这意味着其他机制,如基因扩增,在大型阵列的进化中可能很重要。因此,仅不等交换本身可能不足以解释卫星DNA。