Systematic functional analysis of Leishmania protein kinases identifies regulators of differentiation or survival.
N BakerCarolina Moura Costa Catta-PretaRachel NeishJovana SadlovaBen PowellE V C Alves-FerreiraV GeogheganJuliana B T CarnielliKatherine NewlingC HughesB VojtkovaJ AnandA MihutPegine B WalradLaurence G WilsonJ W PitchfordPetr VolfJeremy Charles MottramPublished in: Nature communications (2021)
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.
Keyphrases
- genome wide
- life cycle
- genome wide identification
- dna methylation
- protein kinase
- copy number
- single cell
- protein protein
- amino acid
- genome wide analysis
- transcription factor
- binding protein
- high throughput
- randomized controlled trial
- magnetic resonance imaging
- clinical trial
- staphylococcus aureus
- magnetic resonance
- metabolic syndrome
- gene expression
- insulin resistance
- drinking water
- candida albicans
- phase iii
- wild type
- bioinformatics analysis