Vig B K, Paweletz N, Schroeter D
Department of Biology, University of Nevada, Reno 89557.
Cancer Genet Cytogenet. 1989 Apr;38(2):283-96. doi: 10.1016/0165-4608(89)90670-5.
A subpopulation of rat cerebral endothelial cells, designated B1, exhibits an array of multicentric chromosomes. Because of the formation of bridges at anaphase, this cell population produced new types of multicentrics at every cell division. These chromosomes showed kinetochore proteins at every centromeric site and all centromeric regions replicated their DNA at the end of the S phase, more or less simultaneously. A new subpopulation of cells, designated B2, obtained from the original sample frozen at Wayne State University displayed several dicentrics. In contrast to B1 these chromosomes exhibit premature centromere separation as reported for mouse and human cell lines. These B2 dicentrics show only one site of kinetochore protein deposition. The timing of DNA replication around the centric region of prematurely separating centromere is also changed similar to the earlier reported premature DNA synthesis for mouse dicentrics. These observations suggest a universality of relationship between premature centromere separation, a lack of kinetochore formation, and early replication of the centric/pericentric DNA associated with these centromeres. The cause of sudden change from activity to inactivity of these chromosomes, though interesting, is not clear.
大鼠脑内皮细胞的一个亚群,称为B1,呈现出一系列多中心染色体。由于在后期形成桥,这个细胞群体在每次细胞分裂时都会产生新型的多中心染色体。这些染色体在每个着丝粒位点都显示有着丝粒蛋白,并且所有着丝粒区域在S期结束时或多或少同时复制其DNA。从韦恩州立大学冷冻保存的原始样本中获得的一个新的细胞亚群,称为B2,显示出几个双着丝粒染色体。与B1相反,这些染色体表现出如小鼠和人类细胞系中所报道的着丝粒过早分离。这些B2双着丝粒染色体仅显示一个着丝粒蛋白沉积位点。过早分离着丝粒的中心区域周围的DNA复制时间也发生了变化,类似于早期报道的小鼠双着丝粒染色体的过早DNA合成。这些观察结果表明,着丝粒过早分离、着丝粒形成缺失以及与这些着丝粒相关的中心/着丝粒周围DNA的早期复制之间存在普遍关系。这些染色体从活跃突然转变为不活跃的原因虽然有趣,但尚不清楚。