Vig B K, Broccoli D
Department of Biology, University of Nevada, Reno 89557-0015.
Chromosoma. 1988;96(4):311-7. doi: 10.1007/BF00286919.
The dicentric and multicentric chromosomes in L cells and a brain tumor cell line of mouse display only one site of kinetochore formation associated with the 'active' centromere. The accessory or 'inactive' centromeres show premature separation. These cell lines were treated with 10(-6) M 5-bromodeoxyuridine (BrdUrd) followed by anti-BrdUrd antibody to study the pattern of replication of pericentric heterochromatin flanking the active vs inactive centromeres. Regardless of its quantity, heterochromatin around the inactive centromere replicates earlier than that associated with the active centromere. There appears to be a relationship between the timing of separation of a centromere and the timing of replication of pericentric heterochromatin. The premature replication of heterochromatin associated with an inactive centromere may be responsible for its premature separation and, hence, inactivity.
在小鼠的L细胞和一种脑肿瘤细胞系中,双着丝粒染色体和多着丝粒染色体仅显示出一个与“活性”着丝粒相关的动粒形成位点。附属的或“非活性”着丝粒表现出过早分离。用10^(-6) M 5-溴脱氧尿苷(BrdUrd)处理这些细胞系,随后用抗BrdUrd抗体研究活性与非活性着丝粒侧翼的着丝粒周围异染色质的复制模式。无论其数量如何,非活性着丝粒周围的异染色质比与活性着丝粒相关的异染色质更早复制。着丝粒分离的时间与着丝粒周围异染色质的复制时间之间似乎存在关联。与非活性着丝粒相关的异染色质的过早复制可能是其过早分离的原因,因此也是其无活性的原因。