Vagnarelli P B, Earnshaw W C
Wellcome Institute for Cell Biology, Institute for Cell and Molecular Biology, University of Edinburgh, Swann Building, Kings Buildings, Mayfield Road, Edinburgh EH9 3JR, UK.
Chromosoma. 2001 Nov;110(6):393-401. doi: 10.1007/s004120100163. Epub 2001 Sep 14.
Inactive centromeres of stable dicentric chromosomes provide a unique opportunity to examine the resolution of sister chromatid cohesion in mitosis. Here we show for the first time that inactive centromeres are composed of heterochromatin, as defined by the presence of heterochromatin protein HP1(Hs alpha). We then show that both the inner centromere protein (INCENP) and its binding partner Aurora-B/AIM-1 kinase can also be detected at the inactive centromere. Thus, targeting of the chromosomal passengers is not dependent upon the presence of an active centromere/kinetochore. Furthermore, we show that the association of INCENP with the inactive centromere correlates strictly with the state of cohesion between sister chromatids: loss of cohesion is accompanied by loss of detectable INCENP. These results are consistent with recent suggestions that one function of the chromosomal passenger proteins may be to regulate sister chromatid separation in mitosis.
稳定的双着丝粒染色体的无活性着丝粒为研究有丝分裂中姐妹染色单体黏连的解离提供了独特的机会。在此,我们首次表明,无活性着丝粒由异染色质组成,这是根据异染色质蛋白HP1(Hsα)的存在来定义的。然后我们表明,在内着丝粒蛋白(INCENP)及其结合伴侣极光激酶B/AIM-1激酶也能在无活性着丝粒处被检测到。因此,染色体乘客蛋白的靶向作用并不依赖于活性着丝粒/动粒的存在。此外,我们表明INCENP与无活性着丝粒的关联与姐妹染色单体之间的黏连状态严格相关:黏连的丧失伴随着可检测到的INCENP的丧失。这些结果与最近的观点一致,即染色体乘客蛋白的一个功能可能是在有丝分裂中调节姐妹染色单体的分离。