A single valine to leucine switch disrupts Plasmodium falciparum AP2-G DNA binding and reveals GDV1's role in ap2-g activation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41547993.
- Also identified by DOI 10.1038/s41467-026-68416-1 and PMC identifier 12913604.
- Licence recorded as CC BY-NC-ND.
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Abstract
Sexual commitment in Plasmodium parasites is essential for malaria transmission, yet the signaling events initiating sexual conversion in only a subpopulation of parasites remain unclear. We discovered a single valine(V<sub>2163</sub>) to leucine(L<sub>2163</sub>) mutation in a transcription factor required for P. falciparum gametocytogenesis (AP2-G) that abrogates sexual differentiation. AP2-G.L<sub>2163</sub> does not bind the ap2-g consensus motif, GnGTAC, or stimulate gene transcription, including autoregulation. The GDV1-dependent expression of AP2-G.L<sub>2163</sub> demonstrates GDV1's critical role in the initial activation of the silent ap2-g locus in the absence of functional AP2-G. While AP2-G.V<sub>2163</sub> is required for MSRP1 expression, providing a marker that discriminates early from late sexually committed schizonts. Together this work demonstrates that V<sub>2163</sub> in AP2-G plays a critical role in DNA binding, highlighting the functional importance of this specific region for malaria transmission as well as the key role of GDV1 in the initial activation of ap2-g expression and induction of sexual differentiation.
Medical subject headings
- Plasmodium falciparum
- Protozoan Proteins
- Leucine
- Transcription Factors
- Valine
- DNA, Protozoan
- DNA-Binding Proteins