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首页> 外文期刊>Cell Division >Rad53 homologue forkhead-associated kinase A (FhkA) and Ca2+-binding protein 4a (CBP4a) are nucleolar proteins that differentially redistribute during mitosis in Dictyostelium
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Rad53 homologue forkhead-associated kinase A (FhkA) and Ca2+-binding protein 4a (CBP4a) are nucleolar proteins that differentially redistribute during mitosis in Dictyostelium

机译:Rad53同源叉头相关激酶A(FhkA)和Ca2 +结合蛋白4a(CBP4a)是核仁蛋白,在网状线粒体的有丝分裂过程中差异性重新分布

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Background During mitosis most nucleolar proteins redistribute to other locales providing an opportunity to study the relationship between nucleolar protein localization and function. Dictyostelium is a model organism for the study of several fundamental biological processes and human diseases but only two nucleolar proteins have been studied during mitosis: NumA1 and Snf12. Both of them are linked to the cell cycle. To acquire a better understanding of nucleolar protein localization and dynamics in Dictyostelium we studied the nucleolar localization of two additional proteins during mitosis: Snf12-linked forkhead-associated kinase A (FhkA), which is involved in the cell cycle, and Ca2+-binding protein 4a (CBP4a), which is a binding partner of NumA1. Methods Polyclonal antibodies were produced in-house. Cells were fixed and probed with either anti-FhkA or anti-CBP4a in order to determine cellular localization during interphase and throughout the stages of mitosis. Colocalization with DAPI nuclear stain allowed us to determine the location of the nucleus and nucleolus while colocalization with anti-α-tubulin allowed us to determine the cell cycle stage. Results Here we verify two novel nucleolar proteins, Rad53 homologue FhkA which localized around the edge of the nucleolus and CBP4a which was detected throughout the entire nucleolus. Treatment with the Ca2+ chelator BAPTA (5?mM) showed that the nucleolar localization of CBP4a is Ca2+-dependent. In response to actinomycin D (0.05?mg/mL) CBP4a disappeared from the nucleolus while FhkA protruded from the nucleus, eventually pinching off as cytoplasmic circles. FhkA and CBP4a redistributed differently during mitosis. FhkA redistributed throughout the entire cell and at the nuclear envelope region from prometaphase through telophase. In contrast, during prometaphase CBP4a relocated to many large, discrete “CBP4a islands” throughout the nucleoplasm. Two larger “CBP4a islands” were also detected specifically at the metaphase plate region. Conclusions FhkA and CBP4a represent the sixth and seventh nucleolar proteins that have been verified to date in Dictyostelium and the third and fourth studied during mitosis. The protein-specific distributions of all of these nucleolar proteins during interphase and mitosis provide unique insight into nucleolar protein dynamics in this model organism setting the stage for future work.
机译:背景技术在有丝分裂过程中,大多数核仁蛋白会重新分布到其他位置,从而提供了研究核仁蛋白定位与功能之间关系的机会。 Dictyostelium是用于研究几种基本生物学过程和人类疾病的模型生物,但在有丝分裂期间仅研究了两种核仁蛋白:NumA1和Snf12。它们都与细胞周期有关。为了更好地了解盘基网柄菌中核仁蛋白的定位和动力学,我们研究了有丝分裂期间另外两种蛋白的核仁定位:Snf12连锁的叉头相关激酶A(FhkA),其参与细胞周期; Ca 2 + 结合蛋白4a(CBP4a),是NumA1的结合伴侣。方法多克隆抗体是在内部产生的。固定细胞并用抗FhkA或抗CBP4a进行探测,以确定在相间和整个有丝分裂阶段的细胞定位。与DAPI核染色剂的共定位使我们能够确定核和核仁的位置,而与抗α-微管蛋白的共定位使我们能够确定细胞周期阶段。结果在这里,我们验证了两个新颖的核仁蛋白,Rad53同源蛋白FhkA,位于核仁边缘,CBP4a遍布整个核仁。用Ca 2 + 螯合剂BAPTA(5?mM)处理表明CBP4a的核仁定位是Ca 2 + 依赖性的。响应放线菌素D(0.05?mg / mL),CBP4a从核仁中消失,而FhkA从细胞核突出,最终以胞质环的形式夹住。在有丝分裂期间,FhkA和CBP4a的分布不同。 FhkA从前中期到末期重新分布在整个细胞内以及核膜区域。相反,在中期前,CBP4a移至整个核质中许多大的,离散的“ CBP4a岛”。还专门在中期板区域检测到两个较大的“ CBP4a岛”。结论FhkA和CBP4a代表迄今已在Dictyostelium中验证的第六和第七核仁蛋白,以及在有丝分裂期间已研究的第三和第四核仁蛋白。在相间和有丝分裂期间,所有这些核仁蛋白的蛋白特异性分布为这种模型生物中的核仁蛋白动力学提供了独特的见解,为将来的工作奠定了基础。

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