Comment[ArrayExpressAccession] E-MTAB-1715 MAGE-TAB Version 1.1 Investigation Title Tbrucei_H1_RNAi Comment[Submitted Name] Tbrucei_H1_RNAi Experiment Description Our goal was to determine if histone H1 is involved in transcription regulation. RNA interference was used to deplete histone H1 from bloodstream form T. brucei in culture. Total RNA was extracted and RNAseq was used to compare the expression profile of H1 depleted clones and parental cell-line. Experimental Design biological variation design cellular modification design Comment[AEExperimentType] RNA-seq of coding RNA Comment[AEExperimentDisplayName] RNA-seq of coding RNA in bloodstream form of Trypanosoma brucei with or without depletion of histone H1 by RNA intereference to study if histone H1 is involved in transcription regulation Experimental Factor Name RNA interference Experimental Factor Type RNA interference Quality Control Type biological replicate Quality Control Term Source REF EFO Public Release Date 2014-07-10 Person Last Name Manso Person First Name Helena Person Mid Initials Person Email hmanso@fm.ul.pt Person Phone 00 351 217 999 561 Person Address Avenida Porofessor Egas Moniz, Edificio Egas Moniz, 1649-028 Lisboa, Portugal Person Affiliation Avenida Porofessor Egas Moniz, Edificio Egas Moniz, 1649-028 Lisboa, Portugal Person Roles submitter PubMed ID Publication Author List Ana C. Pena, Mafalda R. Pimentel, Helena Manso, Rita Vaz-Drago, Daniel Neves, Francisco Aresta-Branco, Filipa R. Ferreira, Fabien Guegan, Luis Pedro Coelho, Maria Carmo-Fonseca, Nuno L. Barbosa-Morais, Luisa M. Figueiredo Publication Title Trypanosoma brucei histone H1 inhibits RNA Polymerase I transcription and is important for parasite fitness in vivo Publication Status Protocol Name P-MTAB-33258 P-MTAB-33259 P-MTAB-33260 P-MTAB-33261 P-MTAB-33262 Protocol Type growth protocol treatment protocol nucleic acid extraction protocol nucleic acid library construction protocol nucleic acid sequencing protocol Protocol Description T. brucei bloodstream form parasites (strain Lister 427, antigenic type MiTat 1.2, clone 221a) [Johnson and Cross, 1979] were cultured at 37 degrees C, 5% CO2, in HMI-11 medium. RNA interference of histone H1 was induced for 4 days in culture. Total RNA was extracted using TRIzol standard protocol. Ribosomal RNA was depleted with RiboMinus kit (Invitrogen). PolyA-containing RNA was purified using Dynabeads oligo-(dT) (Invitrogen) and cDNA was synthesized using random hexamers according to Complete RNA-seq Library System kit (NuGEN) instructions. Illumina HiSeq2000 standard protocol Protocol Term Source REF EFO EFO EFO EFO EFO Protocol Hardware Illumina HiSeq 2000 Term Source Name EFO Term Source File http://www.ebi.ac.uk/efo Comment[SecondaryAccession] ERP003403 Comment[SequenceDataURI] http://www.ebi.ac.uk/ena/data/view/ERR556936-ERR556939 SDRF File E-MTAB-1715.sdrf.txt