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由于连锁有害突变对重组率修饰因子的选择。

Selection on a modifier of recombination rate due to linked deleterious mutations.

作者信息

Pálsson S

机构信息

Department of Conservation Biology and Genetics, Uppsala, Sweden.

出版信息

J Hered. 2002 Jan-Feb;93(1):22-6. doi: 10.1093/jhered/93.1.22.

Abstract

Several models have been suggested to explain the origin and maintenance of recombination. Here I present the results from computer simulations of multilocus haploid and diploid genotypes in small populations. Each chromosome consisted of 1001 loci where deleterious mutations occurred. At "equilibrium" for mutation-selection-genetic drift balance a single recombination variant was introduced to the population in the middle of a chromosome. On average 75,000 replicates for each combination of parameters were followed to fixation or loss of the modifier allele. The results show that, in a small population, increased recombination can be selected, even in the absence of epistasis or beneficial mutations. The effect of the mutation rate for deleterious mutations depends on the ploidy level and the recessiveness of deleterious mutations. A higher deleterious mutation rate is required for an increase in recombination rate to be favored in haploid populations. Increased recombination could not evolve in the case of strong associative overdominance.

摘要

已经提出了几种模型来解释重组的起源和维持。在这里,我展示了小群体中多位点单倍体和二倍体基因型的计算机模拟结果。每条染色体由1001个发生有害突变的位点组成。在突变 - 选择 - 遗传漂变平衡的“平衡”状态下,一个单一的重组变体被引入到染色体中间的群体中。对于每种参数组合,平均跟踪75000次重复实验,直至修饰等位基因固定或丢失。结果表明,在小群体中,即使没有上位性或有益突变,增加的重组也可以被选择。有害突变的突变率的影响取决于倍性水平和有害突变的隐性程度。在单倍体群体中,要使重组率增加受到青睐,需要更高的有害突变率。在强关联超显性的情况下,增加的重组无法进化。

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