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Culture adaptation of malaria parasites selects for convergent loss-of-function mutants
by
Conway, David J.
, Claessens, Antoine
, Affara, Muna
, Kwiatkowski, Dominic P.
, Assefa, Samuel A.
in
631/208
/ 631/326/417/2551
/ Adaptation
/ Adaptation, Physiological - genetics
/ Alleles
/ Animals
/ Biochemistry, Molecular Biology
/ Codon, Nonsense - genetics
/ Codons
/ Gene disruption
/ Genes
/ Genetics
/ Genome
/ Genomes
/ Genomics
/ Humanities and Social Sciences
/ Humans
/ Laboratories
/ Life Sciences
/ Loss of Function Mutation - genetics
/ Malaria
/ Malaria, Falciparum - parasitology
/ Microbiology and Parasitology
/ multidisciplinary
/ Mutation
/ Nucleotide sequence
/ Parasites
/ Parasites - isolation & purification
/ Parasites - physiology
/ Parasitology
/ Plasmodium falciparum
/ Plasmodium falciparum - genetics
/ Plasmodium falciparum - growth & development
/ Plasmodium falciparum - isolation & purification
/ Plasmodium falciparum - physiology
/ Polymorphism, Single Nucleotide - genetics
/ Population genetics
/ Populations and Evolution
/ Science
/ Science (multidisciplinary)
/ Sequence Analysis, DNA
/ Single-nucleotide polymorphism
/ Stop codon
/ Vector-borne diseases
2017
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Culture adaptation of malaria parasites selects for convergent loss-of-function mutants
by
Conway, David J.
, Claessens, Antoine
, Affara, Muna
, Kwiatkowski, Dominic P.
, Assefa, Samuel A.
in
631/208
/ 631/326/417/2551
/ Adaptation
/ Adaptation, Physiological - genetics
/ Alleles
/ Animals
/ Biochemistry, Molecular Biology
/ Codon, Nonsense - genetics
/ Codons
/ Gene disruption
/ Genes
/ Genetics
/ Genome
/ Genomes
/ Genomics
/ Humanities and Social Sciences
/ Humans
/ Laboratories
/ Life Sciences
/ Loss of Function Mutation - genetics
/ Malaria
/ Malaria, Falciparum - parasitology
/ Microbiology and Parasitology
/ multidisciplinary
/ Mutation
/ Nucleotide sequence
/ Parasites
/ Parasites - isolation & purification
/ Parasites - physiology
/ Parasitology
/ Plasmodium falciparum
/ Plasmodium falciparum - genetics
/ Plasmodium falciparum - growth & development
/ Plasmodium falciparum - isolation & purification
/ Plasmodium falciparum - physiology
/ Polymorphism, Single Nucleotide - genetics
/ Population genetics
/ Populations and Evolution
/ Science
/ Science (multidisciplinary)
/ Sequence Analysis, DNA
/ Single-nucleotide polymorphism
/ Stop codon
/ Vector-borne diseases
2017
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Culture adaptation of malaria parasites selects for convergent loss-of-function mutants
by
Conway, David J.
, Claessens, Antoine
, Affara, Muna
, Kwiatkowski, Dominic P.
, Assefa, Samuel A.
in
631/208
/ 631/326/417/2551
/ Adaptation
/ Adaptation, Physiological - genetics
/ Alleles
/ Animals
/ Biochemistry, Molecular Biology
/ Codon, Nonsense - genetics
/ Codons
/ Gene disruption
/ Genes
/ Genetics
/ Genome
/ Genomes
/ Genomics
/ Humanities and Social Sciences
/ Humans
/ Laboratories
/ Life Sciences
/ Loss of Function Mutation - genetics
/ Malaria
/ Malaria, Falciparum - parasitology
/ Microbiology and Parasitology
/ multidisciplinary
/ Mutation
/ Nucleotide sequence
/ Parasites
/ Parasites - isolation & purification
/ Parasites - physiology
/ Parasitology
/ Plasmodium falciparum
/ Plasmodium falciparum - genetics
/ Plasmodium falciparum - growth & development
/ Plasmodium falciparum - isolation & purification
/ Plasmodium falciparum - physiology
/ Polymorphism, Single Nucleotide - genetics
/ Population genetics
/ Populations and Evolution
/ Science
/ Science (multidisciplinary)
/ Sequence Analysis, DNA
/ Single-nucleotide polymorphism
/ Stop codon
/ Vector-borne diseases
2017
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Culture adaptation of malaria parasites selects for convergent loss-of-function mutants
Journal Article
Culture adaptation of malaria parasites selects for convergent loss-of-function mutants
2017
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Overview
Cultured human pathogens may differ significantly from source populations. To investigate the genetic basis of laboratory adaptation in malaria parasites, clinical Plasmodium falciparum isolates were sampled from patients and cultured
in vitro
for up to three months. Genome sequence analysis was performed on multiple culture time point samples from six monoclonal isolates, and single nucleotide polymorphism (SNP) variants emerging over time were detected. Out of a total of five positively selected SNPs, four represented nonsense mutations resulting in stop codons, three of these in a single ApiAP2 transcription factor gene, and one in SRPK1. To survey further for nonsense mutants associated with culture, genome sequences of eleven long-term laboratory-adapted parasite strains were examined, revealing four independently acquired nonsense mutations in two other ApiAP2 genes, and five in Epac. No mutants of these genes exist in a large database of parasite sequences from uncultured clinical samples. This implicates putative master regulator genes in which multiple independent stop codon mutations have convergently led to culture adaptation, affecting most laboratory lines of
P. falciparum
. Understanding the adaptive processes should guide development of experimental models, which could include targeted gene disruption to adapt fastidious malaria parasite species to culture.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Adaptation, Physiological - genetics
/ Alleles
/ Animals
/ Biochemistry, Molecular Biology
/ Codons
/ Genes
/ Genetics
/ Genome
/ Genomes
/ Genomics
/ Humanities and Social Sciences
/ Humans
/ Loss of Function Mutation - genetics
/ Malaria
/ Malaria, Falciparum - parasitology
/ Microbiology and Parasitology
/ Mutation
/ Parasites - isolation & purification
/ Plasmodium falciparum - genetics
/ Plasmodium falciparum - growth & development
/ Plasmodium falciparum - isolation & purification
/ Plasmodium falciparum - physiology
/ Polymorphism, Single Nucleotide - genetics
/ Science
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