Abstract
During its red blood cell stage, the malaria parasite Plasmodium falciparum can switch its variant surface proteins (P. falciparum erythrocyte membrane protein 1) to evade the host immune response. The var gene family encodes P. falciparum erythrocyte membrane protein 1, different versions of which have unique binding specificities to various human endothelial surface molecules. Individual parasites each contain approximately 60 var genes at various locations within their chromosomes; however, parasite isolates contain different complements of var genes, thus, the gene family is enormous with a virtually unlimited number of members. A single var gene is expressed by each parasite in a mutually exclusive manner. We report that control of var gene transcription and antigenic variation is associated with a chromatin memory that includes methylation of histone H3 at lysine K9 as an epigenetic mark. We also discuss how gene transcription memory may affect the mechanism of pathogenesis and immune evasion.
MeSH Terms
Animals
Chromatin/genetics,metabolism
Epigenesis, Genetic/genetics
Gene Expression Regulation
Histones/metabolism
Malaria/immunology,parasitology
Methylation
Plasmodium falciparum/genetics,immunology,pathogenicity
Transcription, Genetic/genetics
Virulence/genetics
Chemicals
Chromatin
Histones
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Chookajorn Thanat
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA.
[email protected]
Dzikowski Ron
Frank Matthias
Li Felomena
Jiwani Alisha Z
Hartl Daniel L
Deitsch Kirk W
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