| Literature DB >> 24411171 |
Qing Zhou1, Huiqing Hu1, Ziyin Li2.
Abstract
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.Entities:
Keywords: Cytokinesis; Genomic stability; Human sleeping sickness; Mitosis; Trypanosome-specific proteins; Trypanosomes
Mesh:
Year: 2014 PMID: 24411171 PMCID: PMC4374570 DOI: 10.1016/B978-0-12-800097-7.00004-X
Source DB: PubMed Journal: Int Rev Cell Mol Biol ISSN: 1937-6448 Impact factor: 6.813