Carvalho Ana, Carmena Mar, Sambade Clara, Earnshaw William C, Wheatley Sally P
Chromosome Structure Group, Wellcome Trust Centre for Cell Biology, Institute of Cell and Molecular Biology, University of Edinburgh, King's Buildings, Mayfield Road, Edinburgh EH9 3JR, Scotland, UK.
J Cell Sci. 2003 Jul 15;116(Pt 14):2987-98. doi: 10.1242/jcs.00612. Epub 2003 Jun 3.
Survivin is an essential chromosomal passenger protein whose function remains unclear. Here, we have used RNA interference to specifically repress Survivin in cultured HeLa cells. Immunoblot analysis showed that Survivin was no longer detectable in cultures 60 hours after transfection with Survivin-specific siRNA. Live cell analysis showed that many Survivin-depleted cells were delayed in mitosis, and immunofluorescence analysis of fixed specimens revealed that Survivin-depleted cells accumulated in prometaphase with misaligned chromosomes. The chromosomal passenger proteins, INCENP and Aurora-B, which can interact directly with Survivin, were absent from the centromeres of Survivin-depleted cells. These data contribute to the emerging picture that Survivin operates together with INCENP and Aurora-B to perform its mitotic duties. Some Survivin-depleted cells eventually exited mitosis without completing cytokinesis. This resulted in a gradual increase in the percentage of multinucleated cells in the culture. Time-lapse imaging of synchronized cultures revealed that control and Survivin-depleted cells arrested in mitosis in the presence of nocodazole; however, the latter failed to arrest in mitosis when treated with taxol. Immunofluorescence studies revealed that Survivin-depleted cells were unable to stably maintain BubR1 at the kinetochores in the presence of either taxol or nocodazole. Our data reveal that Survivin is not required for the spindle assembly checkpoint when it is activated by the loss of microtubules. However, Survivin is required for the maintenance of the checkpoint when it is activated by taxol, which is generally thought to cause a loss of spindle tension.
存活素是一种重要的染色体乘客蛋白,其功能尚不清楚。在此,我们利用RNA干扰技术在培养的HeLa细胞中特异性抑制存活素。免疫印迹分析表明,用存活素特异性小干扰RNA转染60小时后,培养物中不再能检测到存活素。活细胞分析表明,许多缺乏存活素的细胞在有丝分裂中延迟,固定标本的免疫荧光分析显示,缺乏存活素的细胞在前中期积累,染色体排列紊乱。可直接与存活素相互作用的染色体乘客蛋白INCENP和极光激酶B在缺乏存活素的细胞的着丝粒中缺失。这些数据有助于形成这样一种新的认识,即存活素与INCENP和极光激酶B共同发挥作用来履行其有丝分裂职责。一些缺乏存活素的细胞最终未完成胞质分裂就退出了有丝分裂。这导致培养物中多核细胞的百分比逐渐增加。同步培养物的延时成像显示,在诺考达唑存在的情况下,对照细胞和缺乏存活素的细胞在有丝分裂中停滞;然而,在用紫杉醇处理时,后者未能在有丝分裂中停滞。免疫荧光研究表明,在紫杉醇或诺考达唑存在的情况下,缺乏存活素的细胞无法在动粒处稳定维持BubR1。我们的数据表明,当纺锤体组装检查点因微管缺失而被激活时,存活素并非必需。然而,当检查点因紫杉醇激活时,存活素是维持该检查点所必需的,紫杉醇通常被认为会导致纺锤体张力丧失。