Bernat R L, Borisy G G, Rothfield N F, Earnshaw W C
Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Cell Biol. 1990 Oct;111(4):1519-33. doi: 10.1083/jcb.111.4.1519.
We have used autoantibodies to probe the function of three human centromere proteins in mitosis. These antibodies recognize three human polypeptides in immunoblots: CENP-A (17 kD), CENP-B (80 kD), and CENP-C (140 kD). Purified anticentromere antibodies (ACA-IgG) disrupt mitosis when introduced into tissue culture cells during interphase. We have identified two execution points for antibody inhibition. Antibodies injected into the nucleus greater than or equal to 3 h before mitosis prevent the chromosomes from undergoing normal prometaphase movements in the subsequent mitosis. Antibodies injected in the nucleus during late G2 cause cells to arrest in metaphase. Surprisingly, antibodies introduced subsequent to the beginning of prophase do not block mitosis. These results suggest that the CENP antigens are involved in two essential interphase events that are required for centromere action in mitosis. These may include centromere assembly coordinate with the replication of alpha-satellite DNA at the end of S phase and the structural maturation of the kinetochore that begins at prophase.
我们利用自身抗体来探究三种人类着丝粒蛋白在有丝分裂中的功能。这些抗体在免疫印迹中可识别三种人类多肽:着丝粒蛋白A(17千道尔顿)、着丝粒蛋白B(80千道尔顿)和着丝粒蛋白C(140千道尔顿)。在间期将纯化的抗着丝粒抗体(ACA-IgG)导入组织培养细胞时,会破坏有丝分裂。我们已确定了抗体抑制的两个执行点。在有丝分裂前3小时或更早时间注入细胞核的抗体可阻止染色体在随后的有丝分裂中进行正常的前中期运动。在G2晚期注入细胞核的抗体可使细胞停滞在中期。令人惊讶的是,在前期开始后引入的抗体不会阻断有丝分裂。这些结果表明,着丝粒蛋白抗原参与了有丝分裂中着丝粒发挥作用所需的两个重要间期事件。这可能包括在S期结束时与α-卫星DNA复制协调的着丝粒组装以及在前期开始的动粒结构成熟。