Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Semin Cell Dev Biol. 2013 Aug-Sep;24(8-9):653-60. doi: 10.1016/j.semcdb.2013.05.006. Epub 2013 May 21.
If a eukaryotic cell is to reproduce, it must duplicate its genetic information in the form of DNA, and faithfully segregate that information during a complex process of cell division. During this division process, the resulting cells inherit one, and only one, copy of each chromosome. Over thirty years ago, it was predicted that the segregation of sister chromosomes could occur non-randomly, such that a daughter cell would preferentially inherit one of the two sister chromosomes according to some characteristic of that chromosome's template DNA strand. Although this prediction has been confirmed in studies of various cell-types, we know little of both the mechanism by which the asymmetric inheritance occurs and the significance it has to cells. In this essay, we propose a new model of non-random chromosome segregation-the mortal strand hypothesis-and discuss tests of the model that will provide insight into the molecular choreography of this intriguing phenomenon.
如果一个真核细胞要进行繁殖,它必须以 DNA 的形式复制其遗传信息,并在细胞分裂的复杂过程中准确地分离该信息。在这个分裂过程中,产生的细胞各继承一条染色体,而且只能继承一条染色体。三十多年前,人们就预测到姐妹染色体的分离可能是非随机的,即一个子细胞会根据其模板 DNA 链的某种特征,优先继承两条姐妹染色体中的一条。尽管在对各种细胞类型的研究中已经证实了这一预测,但我们对不对称遗传发生的机制及其对细胞的意义知之甚少。在本文中,我们提出了一种新的非随机染色体分离模型——致命链假说,并讨论了对该模型的检验,这将有助于深入了解这一有趣现象的分子舞蹈。