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Ankyrin-1 gene exhibits allelic heterogeneity in conferring protection against Malaria

  • Hong Ming Huang
  • , Denis C. Bauer
  • , Patrick M. Lelliott
  • , Matthew W.A. Dixon
  • , Leann Tilley
  • , Brendan J. McMorran
  • , Simon J. Foote
  • , Gaetan Burgio*
  • *Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    3 Citations (Scopus)

    Abstract

    Allelic heterogeneity is a common phenomenon where a gene exhibits a different phenotype depending on the nature of its genetic mutations. In the context of genes affecting malaria susceptibility, it allowed us to explore and understand the intricate host-parasite interactions during malaria infections. In this study, we described a gene encoding erythrocytic ankyrin-1 (Ank-1) which exhibits allelic-dependent heterogeneous phenotypes during malaria infections. We conducted an ENU mutagenesis screen on mice and identified two Ank-1 mutations, one resulting in an amino acid substitution (MRI95845), and the other a truncated Ank-1 protein (MRI96570). Both mutations caused hereditary spherocytosis-like phenotypes and confer differing protection against Plasmodium chabaudi infections. Upon further examination, the Ank-1(MRI96570) mutation was found to inhibit intraerythrocytic parasite maturation, whereas Ank-1(MRI95845) caused increased bystander erythrocyte clearance during infection. This is the first description of allelic heterogeneity in ankyrin-1 from the direct comparison between two Ank-1 mutations. Despite the lack of direct evidence from population studies, this data further supported the protective roles of ankyrin-1 mutations in conferring malaria protection. This study also emphasized the importance of such phenomena in achieving a better understanding of host-parasite interactions, which could be the basis of future studies.

    Original languageEnglish
    Pages (from-to)3133-3144
    Number of pages12
    JournalG3: Genes, Genomes, Genetics
    Volume7
    Issue number9
    DOIs
    Publication statusPublished - 1 Sept 2017

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