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Evolutionary dynamics in molecular populations of ligase ribozymes.

机译:连接酶核酶分子种群的进化动力学。

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摘要

The emergence of life depended on the ability of the first biopolymer populations to thrive and approach larger population sizes and longer sequences that could store enough information, as required for a cellular type of life. The evolution of these populations very likely occurred under circumstances under which Muller's Ratchet in synergism with random drift could have caused large genetic deterioration of the biopolymers. The genetic deterioration of the molecules caused by the accumulation of mutations occurred during the copying process, can drive the populations to extinction unless there is a mechanism to counteract it. To test the effect of the mutation rate and the effective population size on the time to extinction, we used clonal populations of B16-19 ligase ribozymes, evolved with the continuous evolution in vitro system. The experiments were done using populations of 100, 300, 600 and/or 3000 molecules, and at low and high mutation rates. The error-prone Moloney Murine Leukemia virus reverse transcriptase was used with and without the addition of Mn(II). Populations evolved without Mn(II) were of four effective sizes. The times to extinction for those populations were found to be directly related to the effective size of the population. The small populations approached extinction at an average of 24.3 cycles; while the large populations did so at an average of 44.5 cycles. Genotypic characterization of the populations showed the presence of deleterious mutations in the small populations, which are the likely cause of their genetic deterioration and extinction via mutational meltdown. These deleterious mutations were not observed in the large populations; in contrast an advantageous mutant was present. Populations of 100 and 3000 molecules were evolved with Mn(II). None of the populations showed signs of genetic deterioration nor did they become extinct. Genotypic characterization of the 100-molecule population indicated the presence of a cloud of mutants forming a "quasispecies" structure. The high error rate used generated an extended class of closely genetically-related mutants, as indicated by their Hamming distance. The close connectedness of the mutants facilitates the recovery of one from another in the event of being removed from the population by random genetic drift. Thus, quasispecies shift the target of selection from the individual to the group and through cooperative behavior the populations stay extant. The fitness of the six most abundant molecules evolved was measured. The total fitness of the molecules was measured by identifying the fitness component of the system that affect the ligase replication cycles: the ligation, the reverse transcription and the transcription reactions. It was found that the strength of the three components of fitness varied in different chemical environments, and each has a differential effect in the total absolute fitness of the ligases. The ligase molecules evolved have different total absolute fitness values, and ranged above and below the fitness of B16-19.
机译:生命的出现取决于细胞生命类型所需的首批生物聚合物种群蓬勃发展并接近更大种群规模和更长序列的能力,这些序列可以存储足够的信息。这些种群的进化很可能发生在这样的情况下,在这种情况下,穆勒的棘轮与随机漂移协同作用可能导致生物聚合物的大量遗传降解。在复制过程中发生的由突变积累引起的分子遗传退化,可能导致种群灭绝,除非有某种机制可以阻止它们灭绝。为了测试突变率和有效种群规模对灭绝时间的影响,我们使用了B16-19连接酶核酶的克隆种群,该克隆种群是随着体外系统的不断进化而进化的。实验是使用100、300、600和/或3000个分子的群体进行的,突变率低且高。在添加和不添加Mn(II)的情况下,均使用容易出错的莫洛尼鼠白血病病毒逆转录酶。没有Mn(II)进化的种群有四个有效大小。发现这些种群的灭绝时间与种群的有效规模直接相关。少数群体的平均灭绝周期为24.3个周期。而大批人口平均以44.5个周期这样做。种群的基因型特征表明,小种群中存在有害突变,这可能是其遗传退化和通过突变融化而灭绝的原因。在大量人群中未观察到这些有害突变。相反,存在有利的突变体。 Mn(II)进化出100和3000个分子的种群。没有一个人口显示出遗传退化的迹象,也没有灭绝。 100分子种群的基因型特征表明存在形成“准物种”结构的突变体云。如其汉明距离所示,所使用的高错误率产生了一类扩展的与遗传密切相关的突变体。如果通过随机遗传漂移将其从种群中移出,突变体的紧密联系有助于它们彼此之间的恢复。因此,准种将选择的目标从个人转移到群体,并且通过合作行为,种群得以维持。测量了进化出的六个最丰富的分子的适合度。通过确定影响连接酶复制循环的系统的适合成分来测量分子的总体适合度:连接,逆转录和转录反应。发现适合度的三个成分的强度在不同的化学环境中变化,并且每个都对连接酶的总绝对适合度具有不同的影响。进化出的连接酶分子具有不同的总绝对适应度值,并且在B16-19的适应度之上和之下。

著录项

  • 作者

    Diaz Arenas, Carolina.;

  • 作者单位

    Portland State University.;

  • 授予单位 Portland State University.;
  • 学科 Biology Molecular.;Chemistry Biochemistry.;Biology Evolution and Development.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 153 p.
  • 总页数 153
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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