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相关概念视频

Mismatch Repair01:20

Mismatch Repair

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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Genome Copying Errors02:46

Genome Copying Errors

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DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
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Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
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Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
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Viral Mutations00:36

Viral Mutations

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A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
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在固定之前,随机突变的累积波.

Marius Moeller1, Benjamin Werner2, Weini Huang1,3

  • 1Department of Mathematics, <a href="https://ror.org/026zzn846">Queen Mary University of London</a>, London E14NS, United Kingdom.

Physical review. E
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概括
此摘要是机器生成的。

中性突变经常在种群中固定在一起,形成"突变波". 这些波解释了空频分布,并导致可预测的波频分布,这对于理解进化过程至关重要.

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科学领域:

  • 进化生物学是进化的生物学.
  • 人口遗传学 人口遗传学
  • 分子进化是分子进化的过程.

背景情况:

  • 突变是推动进化的遗传变异的来源.
  • 了解突变固定动态是进化研究的关键.
  • 多个中性突变的关节固定经常发生,与简单的模型相反.

研究的目的:

  • 在常数种群中对中性突变的关节固定事件进行定量分析.
  • 介绍和定义突变"波"的概念.
  • 分析这些突变波的分布和特征.

主要方法:

  • 在随机模拟中对突变固定事件的定量分析.
  • 联合固定分布的统计测量.
  • "突变波"概念的开发和应用.

主要成果:

  • 关节固定事件即使在中性选择下也是常见的.
  • 突变"波"描述了多个突变在特定频率的同时固定.
  • 变异基因频率分布显示了由这些离散突变波主导的大空区域.
  • 一个可预测的"波频分布"从离散波的平均值出现.

结论:

  • 突变波是恒定种群中中性进化的基本特征.
  • 该概念解释了变异性等位基因频率分布中观察到的模式.
  • 波频分布为突变动态提供了一个可预测的模型.