Division of Gene Regulation, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Mol Cell. 2010 May 28;38(4):603-13. doi: 10.1016/j.molcel.2010.03.016.
The three-dimensional organization of chromosomes within the nucleus and its dynamics during differentiation are largely unknown. To visualize this process in molecular detail, we generated high-resolution maps of genome-nuclear lamina interactions during subsequent differentiation of mouse embryonic stem cells via lineage-committed neural precursor cells into terminally differentiated astrocytes. This reveals that a basal chromosome architecture present in embryonic stem cells is cumulatively altered at hundreds of sites during lineage commitment and subsequent terminal differentiation. This remodeling involves both individual transcription units and multigene regions and affects many genes that determine cellular identity. Often, genes that move away from the lamina are concomitantly activated; many others, however, remain inactive yet become unlocked for activation in a next differentiation step. These results suggest that lamina-genome interactions are widely involved in the control of gene expression programs during lineage commitment and terminal differentiation.
细胞核内染色体的三维组织及其在分化过程中的动态变化在很大程度上是未知的。为了在分子水平上详细观察这个过程,我们通过谱系定向神经前体细胞将小鼠胚胎干细胞分化为终末分化的星形胶质细胞,生成了基因组-核纤层相互作用的高分辨率图谱。结果表明,胚胎干细胞中存在的基本染色体结构在谱系定向和随后的终末分化过程中,在数百个位点上逐渐发生改变。这种重塑既涉及单个转录单元,也涉及多基因区域,并影响许多决定细胞身份的基因。通常,远离核纤层的基因会同时被激活;然而,许多其他基因仍然处于非活性状态,但在下一个分化步骤中会被激活。这些结果表明,核纤层-基因组相互作用广泛参与了谱系定向和终末分化过程中基因表达程序的控制。