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TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei

The flagellar pocket (FP) of the pathogen Trypanosoma brucei is an important single copy structure that is formed by the invagination of the pellicular membrane. It is the unique site of endo- and exocytosis and is required for parasite pathogenicity. The FP consists of distinct structural sub-domai...

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Autores principales: Perdomo, Doranda, Berdance, Elodie, Lallinger-Kube, Gertrud, Sahin, Annelise, Dacheux, Denis, Landrein, Nicolas, Cayrel, Anne, Ersfeld, Klaus, Bonhivers, Mélanie, Kohl, Linda, Robinson, Derrick R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: EDP Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906236/
https://www.ncbi.nlm.nih.gov/pubmed/35262485
http://dx.doi.org/10.1051/parasite/2022015
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author Perdomo, Doranda
Berdance, Elodie
Lallinger-Kube, Gertrud
Sahin, Annelise
Dacheux, Denis
Landrein, Nicolas
Cayrel, Anne
Ersfeld, Klaus
Bonhivers, Mélanie
Kohl, Linda
Robinson, Derrick R.
author_facet Perdomo, Doranda
Berdance, Elodie
Lallinger-Kube, Gertrud
Sahin, Annelise
Dacheux, Denis
Landrein, Nicolas
Cayrel, Anne
Ersfeld, Klaus
Bonhivers, Mélanie
Kohl, Linda
Robinson, Derrick R.
author_sort Perdomo, Doranda
collection PubMed
description The flagellar pocket (FP) of the pathogen Trypanosoma brucei is an important single copy structure that is formed by the invagination of the pellicular membrane. It is the unique site of endo- and exocytosis and is required for parasite pathogenicity. The FP consists of distinct structural sub-domains with the least explored being the flagellar pocket collar (FPC). TbBILBO1 is the first-described FPC protein of Trypanosoma brucei. It is essential for parasite survival, FP and FPC biogenesis. In this work, we characterize TbKINX1B, a novel TbBILBO1 partner. We demonstrate that TbKINX1B is located on the basal bodies, the microtubule quartet (a set of four microtubules) and the FPC in T. brucei. Down-regulation of TbKINX1B by RNA interference in bloodstream forms is lethal, inducing an overall disturbance in the endomembrane network. In procyclic forms, the RNAi knockdown of TbKINX1B leads to a minor phenotype with a small number of cells displaying epimastigote-like morphologies, with a misplaced kinetoplast. Our results characterize TbKINX1B as the first putative kinesin to be localized both at the basal bodies and the FPC with a potential role in transporting cargo along with the microtubule quartet.
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spelling pubmed-89062362022-03-24 TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei Perdomo, Doranda Berdance, Elodie Lallinger-Kube, Gertrud Sahin, Annelise Dacheux, Denis Landrein, Nicolas Cayrel, Anne Ersfeld, Klaus Bonhivers, Mélanie Kohl, Linda Robinson, Derrick R. Parasite Research Article The flagellar pocket (FP) of the pathogen Trypanosoma brucei is an important single copy structure that is formed by the invagination of the pellicular membrane. It is the unique site of endo- and exocytosis and is required for parasite pathogenicity. The FP consists of distinct structural sub-domains with the least explored being the flagellar pocket collar (FPC). TbBILBO1 is the first-described FPC protein of Trypanosoma brucei. It is essential for parasite survival, FP and FPC biogenesis. In this work, we characterize TbKINX1B, a novel TbBILBO1 partner. We demonstrate that TbKINX1B is located on the basal bodies, the microtubule quartet (a set of four microtubules) and the FPC in T. brucei. Down-regulation of TbKINX1B by RNA interference in bloodstream forms is lethal, inducing an overall disturbance in the endomembrane network. In procyclic forms, the RNAi knockdown of TbKINX1B leads to a minor phenotype with a small number of cells displaying epimastigote-like morphologies, with a misplaced kinetoplast. Our results characterize TbKINX1B as the first putative kinesin to be localized both at the basal bodies and the FPC with a potential role in transporting cargo along with the microtubule quartet. EDP Sciences 2022-03-09 /pmc/articles/PMC8906236/ /pubmed/35262485 http://dx.doi.org/10.1051/parasite/2022015 Text en © D. Perdomo et al., published by EDP Sciences, 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Perdomo, Doranda
Berdance, Elodie
Lallinger-Kube, Gertrud
Sahin, Annelise
Dacheux, Denis
Landrein, Nicolas
Cayrel, Anne
Ersfeld, Klaus
Bonhivers, Mélanie
Kohl, Linda
Robinson, Derrick R.
TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei
title TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei
title_full TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei
title_fullStr TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei
title_full_unstemmed TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei
title_short TbKINX1B: a novel BILBO1 partner and an essential protein in bloodstream form Trypanosoma brucei
title_sort tbkinx1b: a novel bilbo1 partner and an essential protein in bloodstream form trypanosoma brucei
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906236/
https://www.ncbi.nlm.nih.gov/pubmed/35262485
http://dx.doi.org/10.1051/parasite/2022015
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