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连接姐妹染色单体直至后期开始的DNA连环体由一种检查点机制维持。

DNA catenations that link sister chromatids until the onset of anaphase are maintained by a checkpoint mechanism.

作者信息

Giménez-Abián Juan F, Clarke Duncan J, Giménez-Martín Gonzalo, Weingartner Magdalena, Giménez-Abián M Inmaculada, Carballo Jesús A, Díaz de la Espina Susana Moreno, Bögre László, De la Torre Consuelo

机构信息

Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

出版信息

Eur J Cell Biol. 2002 Jan;81(1):9-16. doi: 10.1078/0171-9335-00226.

Abstract

Treatment of Allium cepa meristematic cells in metaphase with the topoisomerase II inhibitor ICRF-193, results in bridging of the sister chromatids at anaphase. Separation of the sisters in experimentally generated acentric chromosomal fragments was also inhibited by ICRF-193, indicating that some non-centromeric catenations also persist in metaphase chromosomes. Thus, catenations must be resolved by DNA topoisomerase II at the metaphase-to-anaphase transition to allow segregation of sisters. A passive mechanism could maintain catenations holding sisters until the onset of anaphase. At this point the opposite tension exerted on sister chromatids could render the decatenation reaction physically more favorable than catenation. But this possibility was dismissed as acentric chromosome fragments were able to separate their sister chromatids at anaphase. A timing mechanism (a common trigger for two processes taking different times to be completed) could passively couple the resolution of the last remaining catenations to the moment of anaphase onset. This possibility was also discarded as cells arrested in metaphase with microtubule-destabilising drugs still displayed anaphase bridges when released in the presence of ICRF-193. It is possible that a checkpoint mechanism prevents the release of the last catenations linking sisters until the onset of anaphase. To test whether cells are competent to fully resolve catenations before anaphase onset, we generated multinucleate plant cells. In this system, the nuclei within a single multinucleate cell displayed differences in chromosome condensation at metaphase, but initiated anaphase synchronously. When multinucleates were treated with ICRF-193 at the metaphase-toanaphase transition, tangled and untangled anaphases were observed within the same cell. This can only occur if cells are competent to disentangle sister chromatids before the onset of anaphase, but are prevented from doing so by a checkpoint mechanism.

摘要

用拓扑异构酶II抑制剂ICRF - 193处理处于中期的洋葱分生组织细胞,会导致后期姐妹染色单体桥接。实验产生的无着丝粒染色体片段中的姐妹染色单体分离也受到ICRF - 193的抑制,这表明中期染色体中也存在一些非着丝粒连环。因此,在中期到后期的转变过程中,连环必须由DNA拓扑异构酶II解决,以允许姐妹染色单体分离。一种被动机制可以维持连接姐妹染色单体的连环,直到后期开始。此时,施加在姐妹染色单体上的相反张力可能使解连环反应在物理上比连环反应更有利。但这种可能性被排除了,因为无着丝粒染色体片段能够在后期分离其姐妹染色单体。一种定时机制(一个触发两个完成时间不同的过程的共同因素)可以将最后剩余连环的解决与后期开始的时刻被动地联系起来。当用微管去稳定药物使细胞停滞在中期,在ICRF - 193存在下释放时,这些细胞仍显示后期桥,这种可能性也被排除了。有可能存在一种检查点机制,阻止连接姐妹染色单体的最后连环在后期开始前释放。为了测试细胞在后期开始前是否有能力完全解决连环,我们产生了多核植物细胞。在这个系统中,单个多核细胞内的细胞核在中期显示出染色体凝聚的差异,但后期同步启动。当多核细胞在中期到后期转变时用ICRF - 193处理,在同一个细胞内观察到了混乱和不混乱的后期。只有当细胞在后期开始前有能力解开姐妹染色单体,但被检查点机制阻止这样做时,才会发生这种情况。

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