<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter/><organism>Arabidopsis thaliana</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14125</full_dataset_link><description>Comparison analysis of Arabidopsis fbl17-1 single and fbl17-1 e2fc-1 double mutant transcriptomes to study the implication of FBL17 and E2FC in cell cycle regulation and DNA damage responses</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - mRNAs were isolated from total RNAs by using the NEBNext® Poly(A) mRNA Magnetic Isolation Module (NEB) for mRNA libraries preparation. Sequencing libraries were prepared using the Collibri stranded RNA library kit for Illumina (Invitrogen).</sample_protocol><sample_protocol>Growth Protocol - Arabidopsis sterile seeds are plated on MES-buffered Murashige and Skoog) medium (1X MS salts; Duchefa; 0.8% agar, Fluka; 1% (w/v) sucrose; pH adjusted to 5.7 with KOH). Plated seeds are stratified at 4°C for 2-3 days and then transferred to a plant growth chamber under a 16-h-light/8-h-dark cycle (22/20°C) until collection.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNAs were extracted from 10 day-old whole seedlings in vitro-grown by using Trizol solution (Invitrogen) completed by a second phenol/chloroform treatment. Three biological replicates were used as starting material. RNAs concentrations were determined with a QuBit Fluorometer (Thermo Fisher Scientific). RNAs integrities were checked using the 2100 Bioanalyzer (Agilent).</sample_protocol><sample_protocol>Sequencing - The libraries were sequenced using an Illumina Nextseq 500 system (single-end mode 1 × 75 bp).</sample_protocol><sample_protocol>Sample Collection - Whole 10 day-old in vitro-grown seedlings are snap-frozen in liquid nitrogen before RNA extraction.</sample_protocol><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>organisation</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>NextSeq 500</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Arabidopsis thaliana</species><additional_accession>E-MTAB-9050</additional_accession><pubmed_authors>Sandra Noir</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNAseq analysis of Arabidopsis e2fc-1 and fbl17-1 e2fc-1 mutant seedlings</name><description>Comparison analysis of Arabidopsis fbl17-1 single and fbl17-1 e2fc-1 double mutant transcriptomes to study the implication of FBL17 and E2FC in cell cycle regulation and DNA damage responses</description><dates><release>2026-05-31T00:00:00Z</release><modification>2026-05-31T01:01:14.409Z</modification><creation>2024-05-28T21:39:40.083Z</creation></dates><accession>E-MTAB-14125</accession><cross_references><ENA>ERP160716</ENA><Biostudies>E-MTAB-9050</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>