Dai Jun, Sultan Sammy, Taylor Stephen S, Higgins Jonathan M G
Division of Rheumatology, Immunology and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genes Dev. 2005 Feb 15;19(4):472-88. doi: 10.1101/gad.1267105. Epub 2005 Jan 28.
Post-translational modifications of conserved N-terminal tail residues in histones regulate many aspects of chromosome activity. Thr 3 of histone H3 is highly conserved, but the significance of its phosphorylation is unclear, and the identity of the corresponding kinase unknown. Immunostaining with phospho-specific antibodies in mammalian cells reveals mitotic phosphorylation of H3 Thr 3 in prophase and its dephosphorylation during anaphase. Furthermore we find that haspin, a member of a distinctive group of protein kinases present in diverse eukaryotes, phosphorylates H3 at Thr 3 in vitro. Importantly, depletion of haspin by RNA interference reveals that this kinase is required for H3 Thr 3 phosphorylation in mitotic cells. In addition to its chromosomal association, haspin is found at the centrosomes and spindle during mitosis. Haspin RNA interference causes misalignment of metaphase chromosomes, and overexpression delays progression through early mitosis. This work reveals a new kinase involved in composing the histone code and adds haspin to the select group of kinases that integrate regulation of chromosome and spindle function during mitosis and meiosis.
组蛋白中保守的N端尾部残基的翻译后修饰调节染色体活动的许多方面。组蛋白H3的苏氨酸3高度保守,但其磷酸化的意义尚不清楚,相应激酶的身份也未知。在哺乳动物细胞中用磷酸特异性抗体进行免疫染色显示,在前期H3苏氨酸3发生有丝分裂磷酸化,并在后期去磷酸化。此外,我们发现haspin是存在于多种真核生物中的一组独特蛋白激酶的成员,它在体外使H3的苏氨酸3磷酸化。重要的是,通过RNA干扰使haspin缺失表明,这种激酶是有丝分裂细胞中H3苏氨酸3磷酸化所必需的。除了与染色体结合外,在有丝分裂期间还在中心体和纺锤体中发现了haspin。haspin RNA干扰导致中期染色体排列紊乱,过表达会延迟早期有丝分裂的进程。这项工作揭示了一种参与构成组蛋白密码的新激酶,并将haspin添加到在有丝分裂和减数分裂期间整合染色体和纺锤体功能调节的精选激酶组中。