<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Andreas Bachmair</submitter><organism>Arabidopsis thaliana</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-17503</full_dataset_link><description>SUMO conjugation is an important process in developmental transitions and in environmental stress responses. We generated mutants in the key enzyme SUMO conjugating enzyme 1 of Arabidopsis thaliana and investigated how these mutations affect gene expression in leaves. We also combined mutations in SUMO conjugation with expression of a bacterial nahG gene that destroys salicylic acid, to determine which of the differently regulated genes depend on increased salicylic acid levels. The experiment encompasses four biological replicates for each genotype.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Leaves were collected from rosettes of plants with first flowers opening. Leaves were frozen in liquid nitrogen.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Frozen leaf material was crushed with metal beads in a Qiagen TissueLyseer II and used to extract RNA with Promega SV Total RNA Isolation System acc. to manufacturer instructions.</sample_protocol><sample_protocol>Growth Protocol - Plants were grown in a controlled environment climate chamber at 22°C 12/8 day/night cycle at 150 µE light form an LED panel.</sample_protocol><sample_protocol>Sequencing - Sequencing was carried with a NovaSeqX sequencer with 1400M reads.</sample_protocol><sample_protocol>Library Construction - PolyA RNA was enriched using the NEBNext Poly(A) mRNA Magnetic Isolation Module followed by library construction with the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - DEseq2_1.18 was used for normalisation, values at alpha0.05 wer designated as significantly \"up\" or "down\</data_protocol><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>Illumina NovaSeq X</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Arabidopsis thaliana</species><pubmed_authors>Andreas Bachmair</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative RNA expression analysis of Arabidopsis leaf material differing in genes of SUMO conjugation</name><description>SUMO conjugation is an important process in developmental transitions and in environmental stress responses. We generated mutants in the key enzyme SUMO conjugating enzyme 1 of Arabidopsis thaliana and investigated how these mutations affect gene expression in leaves. We also combined mutations in SUMO conjugation with expression of a bacterial nahG gene that destroys salicylic acid, to determine which of the differently regulated genes depend on increased salicylic acid levels. The experiment encompasses four biological replicates for each genotype.</description><dates><release>2026-09-01T00:00:00Z</release><modification>2026-09-01T01:00:53.008Z</modification><creation>2026-08-13T20:17:41.566Z</creation></dates><accession>E-MTAB-17503</accession><cross_references><ENA>ERP203684</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>