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Functional Profiling of a Plasmodium Genome Reveals an Abundance of Essential Genes.
Bushell, Ellen; Gomes, Ana Rita; Sanderson, Theo; Anar, Burcu; Girling, Gareth; Herd, Colin; Metcalf, Tom; Modrzynska, Katarzyna; Schwach, Frank; Martin, Rowena E; Mather, Michael W; McFadden, Geoffrey I; Parts, Leopold; Rutledge, Gavin G; Vaidya, Akhil B; Wengelnik, Kai; Rayner, Julian C; Billker, Oliver.
  • Bushell E; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Gomes AR; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Sanderson T; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Anar B; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Girling G; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Herd C; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Metcalf T; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Modrzynska K; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Schwach F; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Martin RE; Research School of Biology, Australian National University, Canberra, Australia.
  • Mather MW; Drexel University College of Medicine, Philadelphia, PA, USA.
  • McFadden GI; School of Biosciences, University of Melbourne, Royal Parade, Parkville, Australia.
  • Parts L; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Rutledge GG; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK.
  • Vaidya AB; Drexel University College of Medicine, Philadelphia, PA, USA.
  • Wengelnik K; DIMNP, CNRS, INSERM, University Montpellier, Montpellier, France.
  • Rayner JC; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK. Electronic address: julian.rayner@sanger.ac.uk.
  • Billker O; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK. Electronic address: oliver.billker@sanger.ac.uk.
Cell ; 170(2): 260-272.e8, 2017 07 13.
Article en En | MEDLINE | ID: mdl-28708996
ABSTRACT
The genomes of malaria parasites contain many genes of unknown function. To assist drug development through the identification of essential genes and pathways, we have measured competitive growth rates in mice of 2,578 barcoded Plasmodium berghei knockout mutants, representing >50% of the genome, and created a phenotype database. At a single stage of its complex life cycle, P. berghei requires two-thirds of genes for optimal growth, the highest proportion reported from any organism and a probable consequence of functional optimization necessitated by genomic reductions during the evolution of parasitism. In contrast, extreme functional redundancy has evolved among expanded gene families operating at the parasite-host interface. The level of genetic redundancy in a single-celled organism may thus reflect the degree of environmental variation it experiences. In the case of Plasmodium parasites, this helps rationalize both the relative successes of drugs and the greater difficulty of making an effective vaccine.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Plasmodium berghei / Genoma de Protozoos Límite: Animals Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Plasmodium berghei / Genoma de Protozoos Límite: Animals Idioma: En Año: 2017 Tipo del documento: Article