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相关概念视频

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Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
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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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The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
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Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
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Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
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科学领域:

  • 进化生物学
  • 分子生物学
  • 蛋白质生物化学

背景情况:

  • 蛋白质的功能依赖于复杂的组合.
  • 从同质体转变为异质体是通过基因重复发生的.
  • 分子间补偿突变可以在没有适应性进化的情况下驱动这些转变.

研究的目的:

  • 实验性地研究异构复合物从同构酶的演化.
  • 确定基因重复后的有害突变是否会导致新的功能复合体.
  • 了解构造性中立进化的基础机制.

主要方法:

  • 试验基因复制和同质酶的演变.
  • 影响同位素和异位素功能的突变分析.
  • 一个新型异构体的结构确定.

主要成果:

  • 发现了数百种破坏性突变,
  • 这些突变导致重复蛋白的联合表达和异构化.
  • 结构分析揭示了非对称性缓冲功能丧失突变,

结论:

  • 基因重复随之而来的有害突变可以导致功能异构复合物的形成.
  • 建设性中性进化可以在没有适应性进化的情况下发生,由补偿性突变驱动.
  • 蛋白质复杂的进化可以通过结构不对称性促进的子功能化进行.