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莱茵衣藻的重组率变化和不频繁的有性生殖影响遗传多样性。

Recombination Rate Variation and Infrequent Sex Influence Genetic Diversity in Chlamydomonas reinhardtii.

机构信息

Department of Cell and Systems Biology, University of Toronto, Ontario, Canada.

Department of Biology, University of Toronto Mississauga, Ontario, Canada.

出版信息

Genome Biol Evol. 2020 Apr 1;12(4):370-380. doi: 10.1093/gbe/evaa057.

DOI:10.1093/gbe/evaa057
PMID:32181819
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7186780/
Abstract

Recombination confers a major evolutionary advantage by breaking up linkage disequilibrium between harmful and beneficial mutations, thereby facilitating selection. However, in species that are only periodically sexual, such as many microbial eukaryotes, the realized rate of recombination is also affected by the frequency of sex, meaning that infrequent sex can increase the effects of selection at linked sites despite high recombination rates. Despite this, the rate of sex of most facultatively sexual species is unknown. Here, we use genomewide patterns of linkage disequilibrium to infer fine-scale recombination rate variation in the genome of the facultatively sexual green alga Chlamydomonas reinhardtii. We observe recombination rate variation of up to two orders of magnitude and find evidence of recombination hotspots across the genome. Recombination rate is highest flanking genes, consistent with trends observed in other nonmammalian organisms, though intergenic recombination rates vary by intergenic tract length. We also find a positive relationship between nucleotide diversity and physical recombination rate, suggesting a widespread influence of selection at linked sites in the genome. Finally, we use estimates of the effective rate of recombination to calculate the rate of sex that occurs in natural populations, estimating a sexual cycle roughly every 840 generations. We argue that the relatively infrequent rate of sex and large effective population size creates a population genetic environment that increases the influence of selection on linked sites across the genome.

摘要

重组通过打破有害和有益突变之间的连锁不平衡,从而促进选择,赋予了主要的进化优势。然而,在那些仅周期性有性繁殖的物种中,如许多微生物真核生物,实际的重组率也受到性别的频率的影响,这意味着尽管重组率高,但不频繁的性别会增加连锁位点的选择效应。尽管如此,大多数兼性有性物种的性别的频率仍然未知。在这里,我们使用全基因组连锁不平衡的模式来推断兼性有性绿藻莱茵衣藻基因组中精细尺度的重组率变化。我们观察到高达两个数量级的重组率变化,并在整个基因组中发现了重组热点的证据。重组率在侧翼基因处最高,与在其他非哺乳动物生物中观察到的趋势一致,尽管基因间重组率随基因间片段长度而异。我们还发现核苷酸多样性与物理重组率之间存在正相关关系,这表明基因组中连锁位点的选择普遍存在影响。最后,我们利用有效重组率的估计值来计算自然种群中发生的性别的频率,估计大约每 840 代发生一次有性循环。我们认为,相对不频繁的性别的频率和大的有效种群大小创造了一个种群遗传环境,增加了选择对基因组中连锁位点的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/b1bd350e9434/evaa057f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/21e529772855/evaa057f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/8a61248446cf/evaa057f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/b1bd350e9434/evaa057f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/21e529772855/evaa057f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/8a61248446cf/evaa057f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd64/7186780/b1bd350e9434/evaa057f3.jpg

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Genome Biol Evol. 2020 Apr 1;12(4):370-380. doi: 10.1093/gbe/evaa057.
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causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds. across flycatcher populations clarify the causes and consequences of fine-scale recombination rate variation in birds.\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
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Extensive de novo mutation rate variation between individuals and across the genome of Chlamydomonas reinhardtii.莱茵衣藻个体间及全基因组范围内广泛的新生突变率变异。
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Natural Selection and Recombination Rate Variation Shape Nucleotide Polymorphism Across the Genomes of Three Related Populus Species.自然选择与重组率变异塑造了三种相关杨树物种基因组中的核苷酸多态性。
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The ecology and genetics of fitness in Chlamydomonas. VIII. The dynamics of adaptation to novel environments after a single episode of sex.衣藻适应性的生态学与遗传学。VIII. 单次有性生殖事件后对新环境的适应动态。
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Population genomics of the facultatively asexual duckweed Spirodela polyrhiza.兼性无性繁殖浮萍 Spirodela polyrhiza 的群体基因组学研究。
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Beyond recombination: Exploring the impact of meiotic frequency on genome-wide genetic diversity.超越重组:探索减数分裂频率对全基因组遗传多样性的影响。
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Population bottlenecks and sexual recombination shape diatom microevolution.种群瓶颈和有性重组塑造硅藻微观进化。
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Male-biased recombination at chromosome ends in a songbird revealed by precisely mapping crossover positions.

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Patterns of population structure and complex haplotype sharing among field isolates of the green alga Chlamydomonas reinhardtii.绿藻莱茵衣藻田间分离株的种群结构模式和复杂单倍型共享。
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Extreme Lewontin's Paradox in Ubiquitous Marine Phytoplankton Species.普遍海洋浮游植物物种中的极端勒温廷悖论。
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Tetrad analysis in plants and fungi finds large differences in gene conversion rates but no GC bias.
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通过精确定位交叉点揭示一种鸣禽中染色体末端的偏向雄性重组。
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Multiannual patterns of genetic structure and mating type ratios highlight the complex bloom dynamics of a marine planktonic diatom.遗传结构和交配型比例的多年模式突出了一种海洋浮游硅藻复杂的水华动态。
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Population Genomics of the Facultatively Sexual Liverwort Marchantia polymorpha.兼性有性的地钱属植物的群体基因组学。
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Recombination-aware phylogeographic inference using the structured coalescent with ancestral recombination.基于带有祖先重组的结构合并的重组感知系统地理学推断
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Variation in fine-scale recombination rate in temperature-evolved Drosophila melanogaster populations in response to selection.温度驯化的黑腹果蝇种群中精细重组率的变化对选择的响应。
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How Can We Resolve Lewontin's Paradox?我们如何解决莱文廷悖论?
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The distribution of fitness effects of spontaneous mutations in Chlamydomonas reinhardtii inferred using frequency changes under experimental evolution.使用实验进化下的频率变化推断莱茵衣藻自发突变的适应性效应分布。
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Evolutionary Genomics of Sex-Related Chromosomes at the Base of the Green Lineage.绿色线系底部性别相关染色体的进化基因组学。
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在植物和真菌中进行的四联体分析发现,基因转换率存在很大差异,但没有 GC 偏好。
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Variation in recombination frequency and distribution across eukaryotes: patterns and processes.真核生物中重组频率和分布的变化:模式和过程。
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The Recombination Landscape in Wild House Mice Inferred Using Population Genomic Data.利用群体基因组数据推断野生家鼠的重组景观。
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Population genomics of picophytoplankton unveils novel chromosome hypervariability.浮游植物群体基因组揭示了新颖的染色体高度多态性。
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Estimating the parameters of background selection and selective sweeps in in the presence of gene conversion.在存在基因转换的情况下,估计背景选择和选择清扫的参数。
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cyvcf2: fast, flexible variant analysis with Python.cyvcf2:使用Python进行快速、灵活的变异分析。
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Direct Estimate of the Spontaneous Mutation Rate Uncovers the Effects of Drift and Recombination in the Chlamydomonas reinhardtii Plastid Genome.直接估计自发突变率揭示了莱茵衣藻叶绿体基因组中漂变和重组的影响。
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Nonparadoxical evolutionary stability of the recombination initiation landscape in yeast.酵母中重组起始图谱的非矛盾进化稳定性
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