Affinage · Plasmodium

DDX60

PF3D7_0903400 · ATP-dependent RNA helicase DDX60, putative

Annotated
2026-09-08
6 papers in source corpus 1 papers cited in narrative 1 extracted findings

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

PF3D7_0903400 (DDX60) is a putative ATP-dependent RNA helicase of P. falciparum whose only experimental characterization places it within an Md1-associated cytoplasmic ribonucleoprotein complex in gametocytes, where proximity labelling of the male development 1 (Md1) protein recovered DDX60 alongside translational repressors, CCR4–NOT complex members, and other DEAD-box RNA helicases in RNP granule-like structures (PMID:36477538). Beyond this membership in an Md1-proximal RNP environment (PMID:36477538), no direct enzymatic activity, substrate, structure, or independent loss-of-function phenotype has been characterized for DDX60 in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2022 Low

    To place DDX60 in a cellular context, proximity labelling asked which proteins neighbour the male-fate determinant Md1, and recovered DDX60 as a hit, establishing that it resides within an Md1-associated cytoplasmic RNP complex rather than acting in isolation.

    Evidence TurboID proximity labelling followed by mass spectrometry in a P. falciparum Md1-TurboID gametocyte strain versus untagged wild-type control

    PMID:36477538

    Open questions at the time
    • Single proximity-labelling experiment with no direct functional follow-up for DDX60 itself; membership is inferred from spatial proximity, not a validated interaction
    • No ATP-dependent helicase or RNA-binding activity demonstrated for DDX60
    • No independent loss-of-function phenotype for DDX60 established

Open questions

Synthesis pass · forward-looking unresolved questions
  • Whether DDX60 has intrinsic RNA helicase activity, a defined RNA substrate, and a distinct role in gametocyte RNP granule function or male development remains unknown.
  • No biochemical reconstitution of ATP-dependent helicase activity
  • No substrate or interaction partner directly validated
  • No knockdown/knockout phenotype for DDX60 reported

Mechanism profile

Synthesis pass · controlled-vocabulary classification
Complex memberships
Md1-associated cytoplasmic ribonucleoprotein complex [#0]

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2022 PF3D7_0903400 (DDX60) was detected as a biotinylated proximity-labelling hit of the male development 1 (Md1) protein in P. falciparum gametocytes, placing DDX60 in the neighbourhood of cytoplasmic RNP granule-like structures that include translational repressors, CCR4–NOT complex members, and other dead-box RNA helicases. This establishes DDX60's membership in an Md1-associated cytoplasmic ribonucleoprotein complex, but no direct enzymatic activity or independent functional role for DDX60 was demonstrated in this study. TurboID proximity labelling followed by mass spectrometry (Md1-TurboID strain vs. untagged WT control) Nature Low 36477538

Source papers

Stage 0 corpus · 6 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2015 A bioinformatic survey of RNA-binding proteins in Plasmodium. BMC genomics 62 26525978
1968 DNA, RNA , and protein synthesis in erythrocytic forms of Plasmodium knowlesi. The American journal of tropical medicine and hygiene 56 4971014
2024 Cytoadhesion of Plasmodium falciparum-Infected Red Blood Cells Changes the Expression of Cytokine-, Histone- and Antiviral Protein-Encoding Genes in Brain Endothelial Cells. Molecular microbiology 0 39630601
2023 Protein KIC5 is a novel regulator of artemisinin stress response in the malaria parasite Plasmodium falciparum. Scientific reports 0 36624300
2022 Identification of Co-Existing Mutations and Gene Expression Trends Associated With K13-Mediated Artemisinin Resistance in Plasmodium falciparum. Frontiers in genetics 0 35464842
2022 A transcriptional switch controls sex determination in Plasmodium falciparum. Nature 0 36477538