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一个包含 Haspin 和 Aurora B 的正反馈环促进了有丝分裂中着丝粒处 CPC 的积累。

A positive feedback loop involving Haspin and Aurora B promotes CPC accumulation at centromeres in mitosis.

机构信息

Division of Rheumatology, Immunology and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Curr Biol. 2011 Jun 21;21(12):1061-9. doi: 10.1016/j.cub.2011.05.016. Epub 2011 Jun 9.

Abstract

Haspin phosphorylates histone H3 at Thr3 (H3T3ph) during mitosis [1, 2], providing a chromatin binding site for the chromosomal passenger complex (CPC) at centromeres to regulate chromosome segregation [3-5]. H3T3ph becomes increasingly focused at inner centromeres during prometaphase [1, 2], but little is known about how its level or location and the consequent chromosomal localization of the CPC are regulated. In addition, CPC binding to shugoshin proteins contributes to centromeric Aurora B localization [5, 6]. Recruitment of the shugoshins to centromeres requires the phosphorylation of histone H2A at Thr120 (H2AT120ph) by the kinetochore kinase Bub1 [7], but the molecular basis for the collaboration of this pathway with H3T3ph has been unclear. Here, we show that Aurora B phosphorylates Haspin to promote generation of H3T3ph and that Aurora B kinase activity is required for normal chromosomal localization of the CPC, indicating an intimate linkage between Aurora B and Haspin functions in mitosis. We propose that Aurora B activity triggers a CPC-Haspin-H3T3ph feedback loop that promotes generation of H3T3ph on chromatin. We also provide evidence that the Bub1-shugoshin-CPC pathway supplies a signal that boosts the CPC-Haspin-H3T3ph feedback loop specifically at centromeres to produce the well-known accumulation of the CPC in these regions.

摘要

Haspin 在有丝分裂过程中使组蛋白 H3 的 Thr3 发生磷酸化(H3T3ph)[1,2],为着丝粒处的染色体乘客复合物(CPC)提供染色质结合位点,以调节染色体分离[3-5]。在前期,H3T3ph 在内着丝粒处逐渐集中[1,2],但人们对其水平或位置以及 CPC 的相应染色体定位是如何被调节的知之甚少。此外,CPC 与 Sgo2 蛋白的结合有助于着丝粒处 Aurora B 的定位[5,6]。Sgo2 蛋白被招募到着丝粒需要动粒激酶 Bub1 使组蛋白 H2A 的 Thr120 发生磷酸化(H2AT120ph)[7],但这条途径与 H3T3ph 协作的分子基础一直不清楚。在这里,我们表明 Aurora B 使 Haspin 磷酸化以促进 H3T3ph 的生成,并且 Aurora B 激酶活性是 CPC 正常染色体定位所必需的,这表明 Aurora B 和 Haspin 在有丝分裂中的功能之间存在密切联系。我们提出 Aurora B 活性触发 CPC-Haspin-H3T3ph 反馈回路,促进染色质上 H3T3ph 的生成。我们还提供了证据表明,Bub1-Sgo2-CPC 途径提供了一个信号,该信号专门在着丝粒处增强 CPC-Haspin-H3T3ph 反馈回路,从而产生 CPC 在这些区域的众所周知的积累。

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