Vig B K, Zinkowski R P
Cancer Genet Cytogenet. 1986 Aug;22(4):347-59. doi: 10.1016/0165-4608(86)90027-0.
Stable dicentric chromosomes from three mouse cell lines (viz., SEWA Rec4, brain tumor, and L-cells), as well as a human t(9;11) line were analyzed for the sequence in which the two centromeres separate. At prometaphase, as well as in many cells at midmetaphase, the dicentrics express the two centromeres in the form of two primary constrictions. As the cell advances to late metaphase, one of the constrictions loosens the two chromatids so that eventually there is no connection between them. The other centromere stays intact during this period and separates into two units at the metaanaphase junction along with the rest of the genome. The centromere that separates prematurely (out-of-phase) usually is the same in a given dicentric. It is proposed that such a prematurely separating centromere does not function as active element during chromatid migration. Apparently, in dicentrics some sort of control is exerted to eliminate the functioning of one centromere. The nature of such control is not understood at this time. The mouse dicentrics "synthesize" only one kinetochore as definable by antikinetochore antibody studies.
对来自三种小鼠细胞系(即SEWA Rec4、脑肿瘤细胞系和L细胞系)以及一种人类t(9;11)细胞系的稳定双着丝粒染色体进行分析,以确定两个着丝粒分离的顺序。在早中期以及许多处于中期的细胞中,双着丝粒以两个初级缢痕的形式表现出两个着丝粒。随着细胞进入晚中期,其中一个缢痕松开两条染色单体,最终它们之间不再有连接。在此期间,另一个着丝粒保持完整,并在后期连接处与基因组的其他部分一起分离成两个单元。在给定的双着丝粒中,过早(不同步)分离的着丝粒通常是相同的。有人提出,这种过早分离的着丝粒在染色单体迁移过程中不作为活跃元件起作用。显然,在双着丝粒中存在某种控制机制来消除一个着丝粒的功能。目前还不清楚这种控制的本质。通过抗动粒抗体研究可确定,小鼠双着丝粒“合成”仅一个动粒。