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在黑腹果蝇的减数分裂和有丝分裂过程中,Polo激酶调节染色体乘客复合体的定位和活性。

Polo kinase regulates the localization and activity of the chromosomal passenger complex in meiosis and mitosis in Drosophila melanogaster.

作者信息

Carmena Mar, Lombardia Miguel Ortiz, Ogawa Hiromi, Earnshaw William C

机构信息

The Wellcome Trust Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, UK

Centre National de la Recherche Scientifique, Aix-Marseille Université, CNRS UMR 7257, AFMB, 163 Avenue de Luminy, 13288 Marseille, France.

出版信息

Open Biol. 2014 Nov;4(11):140162. doi: 10.1098/rsob.140162.

Abstract

Cell cycle progression is regulated by members of the cyclin-dependent kinase (CDK), Polo and Aurora families of protein kinases. The levels of expression and localization of the key regulatory kinases are themselves subject to very tight control. There is increasing evidence that crosstalk between the mitotic kinases provides for an additional level of regulation. We have previously shown that Aurora B activates Polo kinase at the centromere in mitosis, and that the interaction between Polo and the chromosomal passenger complex (CPC) component INCENP is essential in this activation. In this report, we show that Polo kinase is required for the correct localization and activity of the CPC in meiosis and mitosis. Study of the phenotype of different polo allele combinations compared to the effect of chemical inhibition revealed significant differences in the localization and activity of the CPC in diploid tissues. Our results shed new light on the mechanisms that control the activity of Aurora B in meiosis and mitosis.

摘要

细胞周期进程受细胞周期蛋白依赖性激酶(CDK)、Polo激酶和极光激酶家族的蛋白激酶成员调控。关键调控激酶的表达水平和定位本身受到非常严格的控制。越来越多的证据表明,有丝分裂激酶之间的相互作用提供了额外的调控水平。我们之前已经表明,极光B在有丝分裂过程中在着丝粒处激活Polo激酶,并且Polo与染色体乘客复合体(CPC)组分INCENP之间的相互作用在这种激活中至关重要。在本报告中,我们表明Polo激酶对于CPC在减数分裂和有丝分裂中的正确定位和活性是必需的。与化学抑制的效果相比,对不同polo等位基因组合的表型研究揭示了二倍体组织中CPC的定位和活性存在显著差异。我们的结果为控制减数分裂和有丝分裂中极光B活性的机制提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed80/4248065/ca3ebcd6721e/rsob-4-140162-g1.jpg

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