<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Prof. Artur Scherf</submitter><funding>ParaFrap LabEx</funding><funding>FOSISS-CONACyT</funding><funding>Consejo Nacional de Ciencia y Tecnología (CONACYT)</funding><funding>European Research Council Advanced grant</funding><journal>EMBO Reports</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-SCDT-EMBOR-2018-46331-T</full_dataset_link><abstract>Post-translational modifications of histone H3 N-terminal tails are key epigenetic regulators of virulence gene expression and sexual commitment in the human malaria parasite Plasmodium falciparum. Here, we identify proteolytic clipping of the N-terminal tail of nucleosome-associated histone H3 at amino acid position 21 as a new chromatin modification. A Cathepsin C-like proteolytic clipping activity is observed in nuclear parasite extracts. Notably, an ectopically expressed version of clipped histone H3, PfH3p-HA, is targeted to the nucleus and integrates into mononucleosomes. Furthermore, chromatin immunoprecipitation and next generation sequencing analysis identified PfH3p-HA as being highly enriched in the upstream region of six genes that play a key role in DNA replication and repair:</abstract><repository>biostudies-other</repository><funding_grant_id>228896</funding_grant_id><funding_grant_id>272364</funding_grant_id><funding_grant_id>ANR-11-LABX0024</funding_grant_id><funding_grant_id>PlasmoSilencing 670301</funding_grant_id><pubmed_authors>Dr. Beatriz Xoconostle-Cazares</pubmed_authors><pubmed_authors>Dr. Gabriela, Romero Meza</pubmed_authors><pubmed_authors>Dr. Shruthi, Shidhar Vembar</pubmed_authors><pubmed_authors>Dr. Rafael, Miyazawa Martins</pubmed_authors><pubmed_authors>Rosaura Hernandez-Rivas</pubmed_authors><pubmed_authors>Prof. Artur Scherf</pubmed_authors><pubmed_authors>Ms. Daniela Lozano-Amado</pubmed_authors><pubmed_authors>Miguel Vargas</pubmed_authors><pubmed_authors>Dr. Cameron, Ross MacPherson</pubmed_authors><pubmed_authors>Dr. Abril, Marcela Herrera-Solorio</pubmed_authors><pubmed_authors>Patty Chen</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clipped histone H3 is integrated into nucleosomes of DNA replication genes in the human malaria parasite Plasmodium falciparum</name><description>Post-translational modifications of histone H3 N-terminal tails are key epigenetic regulators of virulence gene expression and sexual commitment in the human malaria parasite Plasmodium falciparum. Here, we identify proteolytic clipping of the N-terminal tail of nucleosome-associated histone H3 at amino acid position 21 as a new chromatin modification. A Cathepsin C-like proteolytic clipping activity is observed in nuclear parasite extracts. Notably, an ectopically expressed version of clipped histone H3, PfH3p-HA, is targeted to the nucleus and integrates into mononucleosomes. Furthermore, chromatin immunoprecipitation and next generation sequencing analysis identified PfH3p-HA as being highly enriched in the upstream region of six genes that play a key role in DNA replication and repair:</description><dates><release>2020-01-16T21:00:10Z</release><modification>2020-01-16T21:00:10Z</modification><creation>2020-01-16T21:00:10Z</creation></dates><accession>S-SCDT-EMBOR-2018-46331-T</accession><cross_references><doi>10.15252/embr.201846331</doi></cross_references></HashMap>