<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Joram Dongus</submitter><organism>Arabidopsis thaliana</organism><software>Nextflow rnaseq rev 3.9</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16910</full_dataset_link><description>This dataset identifies genes expressed in florally induced meristems of Col-0 and skrt-2 plants, in control conditions and during salt stress. It allows us to identify how skrt-2 and salt affect the timing of the floral transition, and how the floral transition itself is regulated.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Treatment - Seven days after sowing, each tray was watered with 800mL of control solution (tap water, no suppletion of NaCl) or 800 mL salt solution that contained 18.40 g NaCl. Each tray contained 21 7x7 cm pots that can take up 3.5 L of water, where the water volume varied between ~ 3 L to ~4.3 L, meaning that the NaCl concentration varied between ~75 mM and ~105 mM NaCl. Afterwards, all plants were well-watered with tap water without added NaCl, to limit salt concentrations becoming too high and excluding water-limiting stress to affect plant phenotypes.</sample_protocol><sample_protocol>Growth Protocol - eeds were stratified in demi-water 4 °C in the dark for 2-4 days and sown directly on standard potting soil. Seeds were covered for 3-4 days with a transparent plastic cover to achieve a high and consistent humidity level and germination. Genotypes were separated from each other in a Latin square design.</sample_protocol><sample_protocol>Library Construction - Total RNA integrity and purity were assessed using an Agilent 5400 by Novogene (UK Co. Ltd (Cambridge, UK)) and subsequently used for RNA poly-A enrichment library preparation and transcriptome</sample_protocol><sample_protocol>Nucleic Acid Extraction - Samples were homogenized using 2 stainless steel beads in 2 mL tubes (SafeSeal; Sarstedt) in a paint shaker (Fast &amp; Fluid) until samples were fully homogenized. RNA isolation was performed using the Universal RNA purification kit (Roboklon; EURx, Berlin, Germany). Possible DNA contaminants were eliminated with an on-column DNaseI digest.</sample_protocol><sample_protocol>Sequencing - sequencing (150bp paired-end mode) on a NovaSeq 6000 platform (Novogene UK Co. Ltd (Cambridge, UK)).</sample_protocol><sample_protocol>Sample Collection - Seven to nine apices per sample were harvested by hand disection between ZT 7.5 and ZT 9.5 in triplicate and snapfrozen in liquid nitrogen and stored at -70 °C.</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>Sequence Alignment - Reads were mapped to the TAIR10 genome (retrieved: 20240308) using the Nextflow (v. 23.04.3) rnaseq pipeline (rev. 3.9; Di Tommaso et al., 2017) yielding 15-75 million reads per sample.</data_protocol><data_protocol>Data Transformation - Normalisation of processed files was performed with the default settings of nextflow/rnaseq 3.9 pipeline. Specifically STAR followed by salmon</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 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Arabidopsis thaliana</species><pubmed_authors>Kilian Duijts</pubmed_authors><pubmed_authors>Christa Testerink</pubmed_authors><pubmed_authors>Joram Dongus</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of SAUERKRAUT and salt on the floral transition in the shoot apex</name><description>This dataset identifies genes expressed in florally induced meristems of Col-0 and skrt-2 plants, in control conditions and during salt stress. It allows us to identify how skrt-2 and salt affect the timing of the floral transition, and how the floral transition itself is regulated.</description><dates><release>2026-09-11T00:00:00Z</release><modification>2026-09-11T07:35:54.072Z</modification><creation>2026-04-15T12:41:08.919Z</creation></dates><accession>E-MTAB-16910</accession><cross_references><ENA>ERP192193</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>