Laboratorio de señalización y mecanismos adaptativos en tripanosomátidos, Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres", Buenos Aires, Argentina.
Departamento de Fisiología, Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
PLoS Negl Trop Dis. 2019 Mar 21;13(3):e0007256. doi: 10.1371/journal.pntd.0007256. eCollection 2019 Mar.
Aurora kinases constitute a family of enzymes that play a key role during metazoan cells division, being involved in events like centrosome maturation and division, chromatin condensation, mitotic spindle assembly, control of kinetochore-microtubule attachments, and cytokinesis initiation. In this work, three Aurora kinase homologues were identified in Trypanosoma cruzi (TcAUK1, -2 and -3), a protozoan parasite of the Kinetoplastida Class. The genomic organization of these enzymes was fully analyzed, demonstrating that TcAUK1 is a single-copy gene, TcAUK2 coding sequence is present in two different forms (short and long) and TcAUK3 is a multi-copy gene. The three TcAUK genes are actively expressed in the different life cycle forms of T. cruzi (amastigotes, trypomastigotes and epimastigotes). TcAUK1 showed a changing localization along the cell cycle of the proliferating epimastigote form: at interphase it is located at the extremes of the kinetoplast while in mitosis it is detected at the cell nucleus, in close association with the mitotic spindle. Overexpression of TcAUK1 in epimastigotes leaded to a delay in the G2/M phases of the cell cycle due a retarded beginning of kinetoplast duplication. By immunofluorescence, we found that when it was overexpressed TcAUK1 lost its localization at the extremes of the kinetoplast during interphase, being observed inside the cell nucleus throughout the entire cell cycle. In summary, TcAUK1 appears to be a functional homologue of human Aurora B kinase, as it is related to mitotic spindle assembling and chromosome segregation. Moreover, TcAUK1 also seems to play a role during the initiation of kinetoplast duplication, a novel role described for this protein.
极光激酶构成一个酶家族,在后生动物细胞分裂过程中发挥关键作用,参与中心体成熟和分裂、染色质浓缩、有丝分裂纺锤体组装、动粒微管连接的控制以及胞质分裂的启动等事件。在这项工作中,在原生动物门的克氏锥虫中鉴定出三种极光激酶同源物(TcAUK1、-2 和 -3)。这些酶的基因组组织得到了全面分析,证明 TcAUK1 是单拷贝基因,TcAUK2 编码序列存在两种不同形式(短和长),而 TcAUK3 是多拷贝基因。这三个 TcAUK 基因在 T. cruzi 的不同生命周期形式(阿米巴型、鞭毛型和上皮型)中均有活性表达。TcAUK1 在增殖上皮型的细胞周期中表现出位置变化:在间期位于动基体的极端,而在有丝分裂中则位于细胞核,与有丝分裂纺锤体紧密相关。在上皮型中过表达 TcAUK1 会导致细胞周期的 G2/M 期延迟,因为动基体的复制开始延迟。通过免疫荧光,我们发现当它过表达时,TcAUK1 在间期失去了在动基体极端的定位,在整个细胞周期中都在细胞核内观察到。总之,TcAUK1 似乎是人类 Aurora B 激酶的功能同源物,因为它与有丝分裂纺锤体组装和染色体分离有关。此外,TcAUK1 似乎在动基体复制的启动中也发挥作用,这是该蛋白的一个新作用。