Nakayasu H, Berezney R
Department of Biological Sciences, State University of New York, Buffalo 14260.
J Cell Biol. 1989 Jan;108(1):1-11. doi: 10.1083/jcb.108.1.1.
We have used fluorescent microscopy to map DNA replication sites in the interphase cell nucleus after incorporation of biotinylated dUTP into permeabilized PtK-1 kangaroo kidney or 3T3 mouse fibroblast cells. Discrete replication granules were found distributed throughout the nuclear interior and along the periphery. Three distinct patterns of replication sites in relationship to chromatin domains in the cell nucleus and the period of S phase were detected and termed type I (early to mid S), type II (mid to late S) and type III (late S). Similar patterns were seen with in vivo replicated DNA using antibodies to 5-bromodeoxyuridine. Extraction of the permeabilized cells with DNase I and 0.2 M ammonium sulfate revealed a striking maintenance of these replication granules and their distinct intranuclear arrangements with the remaining nuclear matrix structures despite the removal of greater than 90% of the total nuclear DNA. The in situ prepared nuclear matrix structures also incorporated biotinylated dUTP into replication granules that were indistinguishable from those detected within the intact nucleus.
我们通过荧光显微镜对生物素化的dUTP掺入通透的PtK - 1袋鼠肾细胞或3T3小鼠成纤维细胞后的间期细胞核中的DNA复制位点进行了定位。发现离散的复制颗粒分布于整个核内及核周边。检测到细胞核中与染色质结构域及S期不同阶段相关的三种不同的复制位点模式,分别称为I型(S期早期至中期)、II型(S期中期至晚期)和III型(S期晚期)。使用抗5 - 溴脱氧尿苷抗体对体内复制的DNA进行检测也观察到了类似的模式。用DNase I和0.2 M硫酸铵对通透细胞进行提取后发现,尽管去除了超过90%的总核DNA,但这些复制颗粒及其在剩余核基质结构中的独特核内排列仍得到了显著维持。原位制备的核基质结构也将生物素化的dUTP掺入到与完整细胞核内检测到的复制颗粒无法区分的复制颗粒中。