{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kanyal A"],"funding":["European Molecular Biology Organization","Francis Crick Institute","Versus Arthritis","European Molecular Biology Organization (EMBO)","Department of Biotechnology, Ministry of Science and Technology, India (DBT)","Wellcome Trust","Department of Biotechnology, Ministry of Science and Technology, India"],"pagination":["e0237723"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11237754"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(6)"],"pubmed_abstract":["<i>Plasmodium falciparum,</i> the deadly protozoan parasite responsible for malaria, has a tightly regulated gene expression profile closely linked to its intraerythrocytic development cycle. Epigenetic modifiers of the histone acetylation code have been identified as key regulators of the parasite's transcriptome but require further investigation. In this study, we map the genomic distribution of <i>Plasmodium falciparum</i> histone deacetylase 1 (PfHDAC1) across the erythrocytic asexual development cycle and find it has a dynamic occupancy over a wide array of developmentally relevant genes. Overexpression of PfHDAC1 results in a progressive increment in parasite load over consecutive rounds of the asexual infection cycle and is associated with enhanced gene expression of multiple famili"],"journal":["mBio"],"pubmed_title":["PfHDAC1 is an essential regulator of <i>P. falciparum</i> asexual proliferation and host cell invasion genes with a dynamic genomic occupancy responsive to artemisinin stress."],"pmcid":["PMC11237754"],"funding_grant_id":["BT/PR41408/MED/29/1547/2020","FC001189","#8640"],"pubmed_authors":["Karmodiya K","Treeck M","Mamatharani DV","Farheen D","Deshmukh B","Davies H","Kanyal A"],"additional_accession":[]},"is_claimable":false,"name":"PfHDAC1 is an essential regulator of <i>P. falciparum</i> asexual proliferation and host cell invasion genes with a dynamic genomic occupancy responsive to artemisinin stress.","description":"<i>Plasmodium falciparum,</i> the deadly protozoan parasite responsible for malaria, has a tightly regulated gene expression profile closely linked to its intraerythrocytic development cycle. Epigenetic modifiers of the histone acetylation code have been identified as key regulators of the parasite's transcriptome but require further investigation. In this study, we map the genomic distribution of <i>Plasmodium falciparum</i> histone deacetylase 1 (PfHDAC1) across the erythrocytic asexual development cycle and find it has a dynamic occupancy over a wide array of developmentally relevant genes. Overexpression of PfHDAC1 results in a progressive increment in parasite load over consecutive rounds of the asexual infection cycle and is associated with enhanced gene expression of multiple famili","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jun","modification":"2025-04-05T15:47:16.154Z","creation":"2025-04-05T15:47:16.154Z"},"accession":"S-EPMC11237754","cross_references":{"pubmed":["38709067"],"doi":["10.1128/mbio.02377-23"]}}