Department of Cell and Systems Biology, University of Toronto, 25 Harbord st,, Toronto, ON M5S 3G5, Canada.
Cell Div. 2013 Apr 12;8(1):4. doi: 10.1186/1747-1028-8-4.
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.
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.
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.
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.
在有丝分裂过程中,大多数核仁蛋白重新分布到其他位置,这为研究核仁蛋白定位与功能之间的关系提供了机会。粘菌是研究几个基本生物学过程和人类疾病的模型生物,但在有丝分裂过程中只研究了两种核仁蛋白:NumA1 和 Snf12。它们都与细胞周期有关。为了更好地理解粘菌中核仁蛋白的定位和动态变化,我们研究了有丝分裂过程中另外两种核仁蛋白的核仁定位:与 Snf12 相关的叉头相关激酶 A(FhkA),它与细胞周期有关,以及钙结合蛋白 4a(CBP4a),它是 NumA1 的结合伴侣。
我们在内部生产了多克隆抗体。为了确定有丝分裂过程中细胞周期各阶段的细胞内定位,用抗 FhkA 或抗 CBP4a 对细胞进行固定和探测。用 DAPI 核染剂进行共定位,以确定核和核仁的位置,用抗 α-微管蛋白进行共定位,以确定细胞周期阶段。
在此,我们验证了两种新的核仁蛋白,Rad53 同源物 FhkA 定位于核仁边缘,CBP4a 则分布于整个核仁。用 Ca2+螯合剂 BAPTA(5mM)处理表明,CBP4a 的核仁定位依赖于 Ca2+。在放线菌酮 D(0.05mg/mL)的作用下,CBP4a 从核仁中消失,而 FhkA 从核中伸出,最终作为细胞质环缢裂。FhkA 和 CBP4a 在有丝分裂过程中重新分布方式不同。FhkA 在整个细胞中重新分布,从前期到末期在核膜区域。相比之下,在前期 CBP4a 重新定位到核质中许多大的、离散的“CBP4a 岛”。在中期板区域还检测到两个较大的“CBP4a 岛”。
FhkA 和 CBP4a 是迄今为止在粘菌中验证的第六种和第七种核仁蛋白,也是第三种和第四种在有丝分裂过程中研究的核仁蛋白。这些核仁蛋白在有丝分裂过程中各期的蛋白特异性分布,为该模型生物的核仁蛋白动力学提供了独特的见解,为未来的工作奠定了基础。