Affinage · Plasmodium

Showing PF3D7_1023900 — CHD1 is a alias.

CHD1

PF3D7_1023900 · chromodomain-helicase-DNA-binding protein 1 homolog, 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_1023900 (CHD1) is a putative chromodomain-helicase-DNA-binding protein of P. falciparum identified as a binding partner of the chromatin-associated protein PfMORC (PF3D7_1468100) by co-immunoprecipitation/mass spectrometry, placing it within a nuclear complex that modulates epigenetic control of gene expression during asexual blood stage development (PMID:39412522). Beyond this complex membership, no direct enzymatic activity, substrate, localization, or independent functional role has been characterized for CHD1 itself in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2024 Medium

    To position CHD1 within P. falciparum chromatin biology, its physical association with the PfMORC complex was established, connecting an otherwise uncharacterized putative chromatin remodeler to a defined epigenetic regulatory machinery.

    Evidence Multi-omic co-immunoprecipitation/mass spectrometry of a PfMORC-HA pulldown in asexual blood stages

    PMID:39412522

    Open questions at the time
    • Single Co-IP/MS without reciprocal validation from a CHD1 tag
    • No direct enzymatic (helicase/remodeling) activity demonstrated for CHD1
    • No genetic or functional assay defining CHD1's independent role or contribution to the complex

Open questions

Synthesis pass · forward-looking unresolved questions
  • Whether CHD1 has intrinsic chromatin-remodeling activity, what genes or genomic loci it acts on, and whether it is functionally required within the PfMORC complex remain unresolved.
  • No demonstrated catalytic activity for CHD1
  • No knockdown/knockout phenotype for CHD1
  • No subcellular localization data specific to CHD1

Mechanism profile

Synthesis pass · controlled-vocabulary classification
Complex memberships
PfMORC-associated chromatin-remodeling complex [#0]

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2024 PF3D7_1023900 (PfCHD1) was identified as a binding partner of PfMORC (PF3D7_1468100) through multi-omic (co-immunoprecipitation/mass spectrometry) analysis, placing CHD1 within a nuclear chromatin-remodeling complex that modulates epigenetic control of gene expression during asexual blood stage development of P. falciparum. Multi-omic analysis including co-immunoprecipitation and mass spectrometry (interactome of PfMORC-HA pulldown) eLife Medium 39412522

Source papers

Stage 0 corpus · 6 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2010 Chromatin-mediated epigenetic regulation in the malaria parasite Plasmodium falciparum. Eukaryotic cell 96 20453074
1986 Rapid repeated DNA replication during microgametogenesis and DNA synthesis in young zygotes of Plasmodium berghei. Transactions of the Royal Society of Tropical Medicine and Hygiene 61 3088783
1968 DNA, RNA , and protein synthesis in erythrocytic forms of Plasmodium knowlesi. The American journal of tropical medicine and hygiene 56 4971014
2005 DNA-[adenine] methylation in lower eukaryotes. Biochemistry. Biokhimiia 42 15948708
2024 A Plasmodium falciparum MORC protein complex modulates epigenetic control of gene expression through interaction with heterochromatin. eLife 13 39412522
2025 A drug repurposing approach reveals targetable epigenetic pathways in Plasmodium vivax hypnozoites. eLife 6 41025349