Abstract

The early divergent protozoan parasite Trypanosoma brucei alternates between the insect vector and the mammalian hosts during its life cycle and proliferates through binary cell fission. The cell cycle control system in T. brucei differs substantially from that in its mammalian hosts and possesses distinct mitosis-cytokinesis checkpoint controls between two life cycle stages, the procyclic form and the bloodstream form. T. brucei undergoes an unusual mode of cytokinesis, which is controlled by a novel signaling cascade consisting of evolutionarily conserved protein kinases and trypanosome-specific regulatory proteins in the procyclic form. However, given the distinct mitosis-cytokinesis checkpoints between the two forms, it is unclear whether the cytokinesis regulatory pathway discovered in the procyclic form also operates in a similar manner in the bloodstream form. Here, we showed that the three regulators of cytokinesis initiation, cytokinesis initiation factor 1 (CIF1), CIF2, and CIF3, are interdependent for subcellular localization but not for protein stability as in the procyclic form. Further, we demonstrated that KLIF, a regulator of cytokinesis completion in the procyclic form, plays limited roles in cytokinesis in the bloodstream form. Finally, we showed that the cleavage furrow-localizing protein FRW1 is required for cytokinesis initiation in the bloodstream form but is nonessential for cytokinesis in the procyclic form. Together, these results identify conserved and life cycle-specific functions of cytokinesis regulators, highlighting the distinction in the regulation of cytokinesis between different life cycle stages of T. bruceiIMPORTANCE The early divergent protozoan parasite Trypanosoma brucei is the causative agent of sleeping sickness in humans and nagana in cattle in sub-Saharan Africa. This parasite has a complex life cycle by alternating between the insect vector and the mammalian hosts and proliferates by binary cell fission. The control of cell division in trypanosomes appears to be distinct from that in its human host and differs substantially between two life cycle stages, the procyclic (insect) form and the bloodstream form. Cytokinesis, the final step of binary cell fission, is regulated by a novel signaling cascade consisting of two evolutionarily conserved protein kinases and a cohort of trypanosome-specific regulators in the procyclic form, but whether this signaling pathway operates in a similar manner in the bloodstream form is unclear. In this report, we performed a functional analysis of multiple cytokinesis regulators and discovered their distinct functions and regulations in the bloodstream form.

Highlights

  • IMPORTANCE The early divergent protozoan parasite Trypanosoma brucei is the causative agent of sleeping sickness in humans and nagana in cattle in sub-Saharan Africa

  • cytokinesis initiation factor 1 (CIF1) was undetectable at any subcellular structures in the G1 phase, but it was found to localize to the new flagellum attachment zone (FAZ) tip after the S phase of the cell cycle when the new FAZ was assembled (Fig. 1A), similar to the localization pattern in the procyclic form [18, 20]

  • To understand the function of CIF1, we carried out RNA interference (RNAi), and Western blotting showed that upon RNAi induction by tetracycline, CIF1 protein level was gradually decreased to ϳ30% of the control level at 24 h of RNAi induction (Fig. 1C)

Read more

Summary

Introduction

Through genetic and biochemical analyses, a signaling pathway underlying cytokinesis initiation in the procyclic form has been delineated, which involves two evolutionarily conserved protein kinases, the T. brucei Polo-like kinase (TbPLK) and the T. brucei Aurora B kinase 1 (TbAUK1), and a cohort of trypanosome-specific proteins [18,19,20,21] These trypanosome-specific proteins include three regulators of cytokinesis initiation, cytokinesis initiation factor 1 (CIF1), CIF2, and CIF3, which form two separate protein complexes, the CIF1-CIF2 complex and the CIF1-CIF3 complex, and localize to the distal tip of the new FAZ to promote cytokinesis initiation [18,19,20,21]. The distinctive positioning of the new flagellum tip between the two life msphere.asm.org 2

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call