Kwan James Z J, Nguyen Thomas F, Teves Sheila S
Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, BC, Canada.
Methods Mol Biol. 2019;2038:239-250. doi: 10.1007/978-1-4939-9674-2_16.
For over two decades, scientists have observed that most transcription factors (TFs) become excluded from mitotic chromosomes of mammalian cells undergoing cell division. The few TFs that were observed to remain bound to chromosomes have been termed mitotic bookmarkers and were predicted to play important roles in reestablishing transcription after mitosis. Using live-cell imaging of endogenous TFs in mouse embryonic stem cells, we discovered that the observed exclusion from mitotic chromosomes is largely a result of formaldehyde cross-linking and that in fact, most TFs bind to mitotic chromosomes throughout mitosis. Here, we describe the single-molecule live-cell imaging and analytical tools we used to characterize and quantify TF diffusion and binding as mouse embryonic stem cells proceed through mitosis.
二十多年来,科学家们观察到,大多数转录因子(TFs)会从正在进行细胞分裂的哺乳动物细胞的有丝分裂染色体中被排除。少数被观察到仍与染色体结合的转录因子被称为有丝分裂书签蛋白,并被预测在有丝分裂后重新建立转录过程中发挥重要作用。通过对小鼠胚胎干细胞中内源性转录因子进行活细胞成像,我们发现观察到的转录因子从有丝分裂染色体中的排除在很大程度上是甲醛交联的结果,而事实上,大多数转录因子在整个有丝分裂过程中都与有丝分裂染色体结合。在这里,我们描述了我们用于表征和量化小鼠胚胎干细胞在有丝分裂过程中转录因子扩散和结合的单分子活细胞成像及分析工具。