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

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          Abstract

          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.

          Abstract

          Protein kinases are fundamental in cellular signalling required for Leishmania survival throughout the life cycle. Here, Baker and Catta-Preta et al. report on a kinome-wide functional study in Leishmania mexicana to define protein kinases with roles in life cycle transition.

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          Most cited references68

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          Cutadapt removes adapter sequences from high-throughput sequencing reads

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            Prioritization of cancer therapeutic targets using CRISPR–Cas9 screens

            Functional genomics approaches can overcome limitations-such as the lack of identification of robust targets and poor clinical efficacy-that hamper cancer drug development. Here we performed genome-scale CRISPR-Cas9 screens in 324 human cancer cell lines from 30 cancer types and developed a data-driven framework to prioritize candidates for cancer therapeutics. We integrated cell fitness effects with genomic biomarkers and target tractability for drug development to systematically prioritize new targets in defined tissues and genotypes. We verified one of our most promising dependencies, the Werner syndrome ATP-dependent helicase, as a synthetic lethal target in tumours from multiple cancer types with microsatellite instability. Our analysis provides a resource of cancer dependencies, generates a framework to prioritize cancer drug targets and suggests specific new targets. The principles described in this study can inform the initial stages of drug development by contributing to a new, diverse and more effective portfolio of cancer drug targets.
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              Mosdepth: quick coverage calculation for genomes and exomes

              Abstract Summary Mosdepth is a new command-line tool for rapidly calculating genome-wide sequencing coverage. It measures depth from BAM or CRAM files at either each nucleotide position in a genome or for sets of genomic regions. Genomic regions may be specified as either a BED file to evaluate coverage across capture regions, or as a fixed-size window as required for copy-number calling. Mosdepth uses a simple algorithm that is computationally efficient and enables it to quickly produce coverage summaries. We demonstrate that mosdepth is faster than existing tools and provides flexibility in the types of coverage profiles produced. Availability and implementation mosdepth is available from https://github.com/brentp/mosdepth under the MIT license. Supplementary information Supplementary data are available at Bioinformatics online.
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                Author and article information

                Contributors
                jeremy.mottram@york.ac.uk
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                23 February 2021
                23 February 2021
                2021
                : 12
                : 1244
                Affiliations
                [1 ]GRID grid.5685.e, ISNI 0000 0004 1936 9668, York Biomedical Research Institute, , University of York, ; York, UK
                [2 ]GRID grid.5685.e, ISNI 0000 0004 1936 9668, Department of Biology, , University of York, ; York, UK
                [3 ]GRID grid.4491.8, ISNI 0000 0004 1937 116X, Department of Parasitology, Faculty of Science, , Charles University, ; Prague, Czech Republic
                [4 ]GRID grid.5685.e, ISNI 0000 0004 1936 9668, Department of Mathematics, , University of York, ; York, UK
                [5 ]GRID grid.5685.e, ISNI 0000 0004 1936 9668, Department of Physics, , University of York, ; York, UK
                Author information
                http://orcid.org/0000-0001-8983-3487
                http://orcid.org/0000-0001-9756-546X
                http://orcid.org/0000-0002-0432-2707
                http://orcid.org/0000-0002-0247-7713
                http://orcid.org/0000-0003-2116-6379
                http://orcid.org/0000-0003-0354-2924
                http://orcid.org/0000-0002-2302-0720
                http://orcid.org/0000-0001-6659-6001
                http://orcid.org/0000-0003-1790-1123
                http://orcid.org/0000-0001-5574-3766
                Article
                21360
                10.1038/s41467-021-21360-8
                7902614
                33623024
                77f0ed37-9792-4972-8e85-7f33217f2b9d
                © 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/.

                History
                : 25 August 2020
                : 13 January 2021
                Categories
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                © The Author(s) 2021

                Uncategorized
                parasite biology,parasite development
                Uncategorized
                parasite biology, parasite development

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