Department of Microbiology and Molecular Genetics, University of Texas Medical School at Houston, Houston, Texas, USA.
Department of Microbiology and Molecular Genetics, University of Texas Medical School at Houston, Houston, Texas, USA.
Int Rev Cell Mol Biol. 2014;308:127-66. doi: 10.1016/B978-0-12-800097-7.00004-X.
Trypanosoma brucei, a unicellular eukaryote and the causative agent of human sleeping sickness, possesses multiple single-copy organelles that all need to be duplicated and segregated during cell division. Trypanosomes undergo a closed mitosis in which the mitotic spindle is anchored on the nuclear envelope and connects the kinetochores made of novel protein components. Cytokinesis in trypanosomes is initiated from the anterior tip of the new flagellum attachment zone, and proceeds along the longitudinal axis without the involvement of the actomyosin contractile ring, the well-recognized cytokinesis machinery conserved from yeast to humans. Trypanosome appears to employ both evolutionarily conserved and trypanosome-specific proteins to regulate its cell cycle, and has evolved certain cell cycle regulatory pathways that are either distinct between its life cycle stages or different from its human host. Understanding the mechanisms of mitosis and cytokinesis in trypanosomes not only would shed novel light on the evolution of cell cycle control, but also could provide new drug targets for chemotherapy.
布氏锥虫,一种单细胞真核生物,也是人类昏睡病的病原体,拥有多个需要在细胞分裂过程中复制和分离的单拷贝细胞器。布氏锥虫经历一种封闭的有丝分裂,其中有丝分裂纺锤体锚定在核膜上,并连接由新型蛋白成分组成的动粒。锥虫的胞质分裂始于新鞭毛附着区的前端,并沿着纵轴进行,而不涉及肌动球蛋白收缩环,这是一种从酵母到人都保守的公认的胞质分裂机制。布氏锥虫似乎利用既进化保守又锥虫特有的蛋白来调节其细胞周期,并进化出某些细胞周期调控途径,这些途径在其生命周期的不同阶段之间是不同的,或者与人类宿主不同。了解锥虫有丝分裂和胞质分裂的机制不仅可以为细胞周期调控的进化提供新的线索,还可以为化疗提供新的药物靶点。