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Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival

Differentiation between distinct stages is fundamental for the life cycle of intracellular protozoan parasites and for transmission between hosts, requiring stringent spatial and temporal regulation. Here, we apply kinome-wide gene deletion and gene tagging in Leishmania mexicana promastigotes to de...

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Autores principales: Baker, N., Catta-Preta, C. M. C., Neish, R., Sadlova, J., Powell, B., Alves-Ferreira, E. V. C., Geoghegan, V., Carnielli, J. B. T., Newling, K., Hughes, C., Vojtkova, B., Anand, J., Mihut, A., Walrad, P. B., Wilson, L. G., Pitchford, J. W., Volf, P., Mottram, J. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902614/
https://www.ncbi.nlm.nih.gov/pubmed/33623024
http://dx.doi.org/10.1038/s41467-021-21360-8
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author Baker, N.
Catta-Preta, C. M. C.
Neish, R.
Sadlova, J.
Powell, B.
Alves-Ferreira, E. V. C.
Geoghegan, V.
Carnielli, J. B. T.
Newling, K.
Hughes, C.
Vojtkova, B.
Anand, J.
Mihut, A.
Walrad, P. B.
Wilson, L. G.
Pitchford, J. W.
Volf, P.
Mottram, J. C.
author_facet Baker, N.
Catta-Preta, C. M. C.
Neish, R.
Sadlova, J.
Powell, B.
Alves-Ferreira, E. V. C.
Geoghegan, V.
Carnielli, J. B. T.
Newling, K.
Hughes, C.
Vojtkova, B.
Anand, J.
Mihut, A.
Walrad, P. B.
Wilson, L. G.
Pitchford, J. W.
Volf, P.
Mottram, J. C.
author_sort Baker, N.
collection PubMed
description Differentiation between distinct stages is fundamental for the life cycle of intracellular protozoan parasites and for transmission between hosts, requiring stringent spatial and temporal regulation. Here, we apply kinome-wide gene deletion and gene tagging in Leishmania mexicana promastigotes to define protein kinases with life cycle transition roles. Whilst 162 are dispensable, 44 protein kinase genes are refractory to deletion in promastigotes and are likely core genes required for parasite replication. Phenotyping of pooled gene deletion mutants using bar-seq and projection pursuit clustering reveal functional phenotypic groups of protein kinases involved in differentiation from metacyclic promastigote to amastigote, growth and survival in macrophages and mice, colonisation of the sand fly and motility. This unbiased interrogation of protein kinase function in Leishmania allows targeted investigation of organelle-associated signalling pathways required for successful intracellular parasitism.
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spelling pubmed-79026142021-03-11 Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival Baker, N. Catta-Preta, C. M. C. Neish, R. Sadlova, J. Powell, B. Alves-Ferreira, E. V. C. Geoghegan, V. Carnielli, J. B. T. Newling, K. Hughes, C. Vojtkova, B. Anand, J. Mihut, A. Walrad, P. B. Wilson, L. G. Pitchford, J. W. Volf, P. Mottram, J. C. Nat Commun Article Differentiation between distinct stages is fundamental for the life cycle of intracellular protozoan parasites and for transmission between hosts, requiring stringent spatial and temporal regulation. Here, we apply kinome-wide gene deletion and gene tagging in Leishmania mexicana promastigotes to define protein kinases with life cycle transition roles. Whilst 162 are dispensable, 44 protein kinase genes are refractory to deletion in promastigotes and are likely core genes required for parasite replication. Phenotyping of pooled gene deletion mutants using bar-seq and projection pursuit clustering reveal functional phenotypic groups of protein kinases involved in differentiation from metacyclic promastigote to amastigote, growth and survival in macrophages and mice, colonisation of the sand fly and motility. This unbiased interrogation of protein kinase function in Leishmania allows targeted investigation of organelle-associated signalling pathways required for successful intracellular parasitism. Nature Publishing Group UK 2021-02-23 /pmc/articles/PMC7902614/ /pubmed/33623024 http://dx.doi.org/10.1038/s41467-021-21360-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Baker, N.
Catta-Preta, C. M. C.
Neish, R.
Sadlova, J.
Powell, B.
Alves-Ferreira, E. V. C.
Geoghegan, V.
Carnielli, J. B. T.
Newling, K.
Hughes, C.
Vojtkova, B.
Anand, J.
Mihut, A.
Walrad, P. B.
Wilson, L. G.
Pitchford, J. W.
Volf, P.
Mottram, J. C.
Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival
title Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival
title_full Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival
title_fullStr Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival
title_full_unstemmed Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival
title_short Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival
title_sort systematic functional analysis of leishmania protein kinases identifies regulators of differentiation or survival
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902614/
https://www.ncbi.nlm.nih.gov/pubmed/33623024
http://dx.doi.org/10.1038/s41467-021-21360-8
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