1] Department of Molecular Cell Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany. [2] Institute of Science and Technology (IST) Austria, 3400 Klosterneuburg, Austria. [3].
1] Department of Molecular Cell Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany. [2].
Nat Rev Mol Cell Biol. 2014 Jun;15(6):369-83. doi: 10.1038/nrm3805. Epub 2014 May 14.
Homologous recombination is crucial for genome stability and for genetic exchange. Although our knowledge of the principle steps in recombination and its machinery is well advanced, homology search, the critical step of exploring the genome for homologous sequences to enable recombination, has remained mostly enigmatic. However, recent methodological advances have provided considerable new insights into this fundamental step in recombination that can be integrated into a mechanistic model. These advances emphasize the importance of genomic proximity and nuclear organization for homology search and the critical role of homology search mediators in this process. They also aid our understanding of how homology search might lead to unwanted and potentially disease-promoting recombination events.
同源重组对于基因组稳定性和遗传交换至关重要。尽管我们对重组及其机制的主要步骤的了解已经很深入,但同源搜索——探索基因组中同源序列以实现重组的关键步骤——仍然很大程度上是个谜。然而,最近的方法学进展为重组这一基本步骤提供了相当多的新见解,可以将这些见解整合到一个机制模型中。这些进展强调了基因组接近性和核组织对同源搜索的重要性,以及同源搜索介质在这个过程中的关键作用。它们还有助于我们理解同源搜索如何导致不必要的、可能促进疾病的重组事件。
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