The protozoan parasite Plasmodium falciparum, responsible for the deadliest form of human malaria, employs antigenic variation via monoallelic expression as a key survival strategy. The selective activation of one out of the 60-member var gene family is key to understanding the parasite's ability to cause severe disease and evade the host immune response. var gene activation is initiated by its relocation to a specialized expression site. While the perinuclear expression site (PES) plays a crucial role in enabling the expression of a single allele, the characteristics of this PES remain largely obscure. Recent breakthroughs in genome editing tools and the discovery of regulatory noncoding RNAs have shed light on this intriguing biological feature, offering significant insights into the mechanisms of pathogen virulence.
Keyphrases
- plasmodium falciparum
- poor prognosis
- gene expression
- crispr cas
- immune response
- genome editing
- escherichia coli
- machine learning
- pseudomonas aeruginosa
- endothelial cells
- small molecule
- deep learning
- long non coding rna
- biofilm formation
- early onset
- dendritic cells
- candida albicans
- genome wide
- inflammatory response
- induced pluripotent stem cells