Huang Hong Ming, Bauer Denis C, Lelliott Patrick M, Dixon Matthew W A, Tilley Leann, McMorran Brendan J, Foote Simon J, Burgio Gaetan
Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Australian National University, Canberra 2601, Australia.
Commonwealth Scientific and Industrial Research Organisation, Sydney 2113, Australia.
G3 (Bethesda). 2017 Sep 7;7(9):3133-3144. doi: 10.1534/g3.117.300079.
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 () which exhibits allelic-dependent heterogeneous phenotypes during malaria infections. We conducted an ENU mutagenesis screen on mice and identified two mutations, one resulting in an amino acid substitution (MRI95845), and the other a truncated protein (MRI96570). Both mutations caused hereditary spherocytosis-like phenotypes and confer differing protection against infections. Upon further examination, the mutation was found to inhibit intraerythrocytic parasite maturation, whereas caused increased bystander erythrocyte clearance during infection. This is the first description of allelic heterogeneity in ankyrin-1 from the direct comparison between two 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.
等位基因异质性是一种常见现象,即一个基因根据其基因突变的性质表现出不同的表型。在影响疟疾易感性的基因背景下,它使我们能够探索和理解疟疾感染期间复杂的宿主-寄生虫相互作用。在本研究中,我们描述了一个编码红细胞锚蛋白-1()的基因,该基因在疟疾感染期间表现出等位基因依赖性的异质表型。我们对小鼠进行了ENU诱变筛选,鉴定出两个突变,一个导致氨基酸替换(MRI95845),另一个导致截短的蛋白(MRI96570)。这两个突变都导致了遗传性球形红细胞增多症样表型,并对感染提供了不同程度的保护。进一步检查发现,突变抑制了红细胞内寄生虫的成熟,而在感染期间导致旁观者红细胞清除增加。这是首次通过对两个突变的直接比较来描述锚蛋白-1中的等位基因异质性。尽管缺乏人群研究的直接证据,但这些数据进一步支持了锚蛋白-1突变在赋予疟疾保护方面的保护作用。本研究还强调了这种现象在更好地理解宿主-寄生虫相互作用方面的重要性,这可能是未来研究的基础。