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孤雌生殖繁殖的钝额溞品系核糖体DNA中的重组率。

Rates of recombination in the ribosomal DNA of apomictically propagated Daphnia obtusa lines.

作者信息

McTaggart Seanna J, Dudycha Jeffry L, Omilian Angela, Crease Teresa J

机构信息

Department of Integrative Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.

出版信息

Genetics. 2007 Jan;175(1):311-20. doi: 10.1534/genetics.105.050229. Epub 2006 Nov 16.

Abstract

Ribosomal (r)DNA undergoes concerted evolution, the mechanisms of which are unequal crossing over and gene conversion. Despite the fundamental importance of these mechanisms to the evolution of rDNA, their rates have been estimated only in a few model species. We estimated recombination rate in rDNA by quantifying the relative frequency of intraindividual length variants in an expansion segment of the 18S rRNA gene of the cladoceran crustacean, Daphnia obtusa, in four apomictically propagated lines. We also used quantitative PCR to estimate rDNA copy number. The apomictic lines were sampled every 5 generations for 90 generations, and we considered each significant change in the frequency distribution of length variants between time intervals to be the result of a recombination event. Using this method, we calculated the recombination rate for this region to be 0.02-0.06 events/generation on the basis of three different estimates of rDNA copy number. In addition, we observed substantial changes in rDNA copy number within and between lines. Estimates of haploid copy number varied from 53 to 233, with a mean of 150. We also measured the relative frequency of length variants in 30 lines at generations 5, 50, and 90. Although length variant frequencies changed significantly within and between lines, the overall average frequency of each length variant did not change significantly between the three generations sampled, suggesting that there is little or no bias in the direction of change due to recombination.

摘要

核糖体(r)DNA经历协同进化,其机制为不等交换和基因转换。尽管这些机制对rDNA的进化至关重要,但仅在少数模式物种中估计过它们的速率。我们通过量化枝角类甲壳动物钝额溞18S rRNA基因扩展片段中个体内长度变异体的相对频率,在四个孤雌生殖繁殖系中估计了rDNA的重组率。我们还使用定量PCR来估计rDNA的拷贝数。每隔5代对孤雌生殖系进行采样,共采样90代,我们将时间间隔之间长度变异体频率分布的每一个显著变化视为重组事件的结果。基于rDNA拷贝数的三种不同估计,我们用这种方法计算出该区域的重组率为0.02 - 0.06次事件/代。此外,我们观察到系内和系间rDNA拷贝数有显著变化。单倍体拷贝数的估计值在53到233之间变化,平均值为150。我们还测量了30个系在第5代、第50代和第90代时长度变异体的相对频率。尽管系内和系间长度变异体频率有显著变化,但在采样的三代之间,每个长度变异体的总体平均频率没有显著变化,这表明由于重组导致的变化方向几乎没有或没有偏差。

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