Institut Pasteur, Stem Cells & Development, Department of Developmental & Stem Cell Biology, CNRS URA 2578, 25 rue du Dr. Roux, Paris F-75015, France.
Semin Cell Dev Biol. 2013 Aug-Sep;24(8-9):627-42. doi: 10.1016/j.semcdb.2013.05.008. Epub 2013 May 13.
The semi-conservative nature of DNA replication has suggested that identical DNA molecules within chromatids are inherited by daughter cells after cell division. Numerous reports of non-random DNA segregation in prokaryotes and eukaryotes suggest that this is not always the case, and that epigenetic marks on chromatids, if not the individual DNA strands themselves, could have distinct signatures. Their selective distribution to daughter cells provides a novel mechanism for gene and cell fate regulation by segregating chromatids asymmetrically. Here we highlight some examples and potential mechanisms that can regulate this process. We propose that cellular asymmetry is inherently present during each cell division, and that it provides an opportunity during each cell cycle for moderating cell fates.
DNA 复制的半保守性质表明,在细胞分裂后,姐妹染色单体中的相同 DNA 分子被子细胞继承。大量关于原核生物和真核生物中非随机 DNA 分离的报告表明,情况并非总是如此,染色单体上的表观遗传标记(如果不是单个 DNA 链本身)可能具有独特的特征。如果将它们有选择地分配到子细胞中,就可以通过不对称地分离染色单体为基因和细胞命运调控提供一种新的机制。在这里,我们重点介绍一些可以调节该过程的示例和潜在机制。我们提出,细胞不对称性在每次细胞分裂中固有存在,并且在每个细胞周期中为调节细胞命运提供了机会。