<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Imani Madison</submitter><organism>Arabidopsis thaliana</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15703</full_dataset_link><description>RNA-seq of pPEAR1::dBOX-YFP, pPEAR1-erGFP, and pC2-YFP to characterize the transcriptome associated with progressively more differentiated sieve elements. pPEAR1::dBOX-YFP is the proxy for early / phloem initials. pPEAR1-erGFP is the proxy for transit amplifying protophloem. pC2-YFP is the proxy for differentiation sieve elements. Each marker line was grown for 4 days in standard MS (Murashige &amp; Skoog) media then transferred to iron deficient media (Murashige &amp; Skoog containing ferrozine to chelate any iron present so that it's biounavailable). At 24h after transfer, roots were protoplasted and sorted using Fluorescence Activated Cell Sorting (FACS) to isolate GFP-positive or YFP-positive cells. Then, RNA-seq was performed in the sorted cell populations.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - FACS-sorted protocols were collected from 5d old roots that had been iron deficiency-starved for 24h</sample_protocol><sample_protocol>Library Construction - Extracted RNA was converted to cDNA using the  Takara SMARTer cDNA synthesis kit</sample_protocol><sample_protocol>Sample Treatment - Plants were transferred to iron deficiency media for 24h before sorting</sample_protocol><sample_protocol>Growth Protocol - Growth on MS for 4d then transferred to iron deficient media for 24h</sample_protocol><sample_protocol>Nucleic Acid Extraction - Sorted cells were immediately frozen on liquid nitrogen then RNA was extracted using the Qiagen RNeasy micro kit</sample_protocol><sample_protocol>Sequencing - Bulk-sorted pooled samples were sequenced by  Illumina sequencing</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 - Expression values of the DEGs were normalized in edgeR (RPKM values)</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 HiSeq 4000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Arabidopsis thaliana</species><pubmed_title>Iron deficiency changes regulatory mechanisms governing sieve element cell differentiation</pubmed_title><pubmed_authors>Imani Madison, Eli D. Buckner, Maria Angels de Luis Balaguer, Jina Song, Dipali Srivastava, Devarshi Selote, Aitch Hunt, Eduardo Bueso, Rosangela Sozzani, Cranos Williams, Terri A. Long</pubmed_authors><pubmed_authors>Imani Madison</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of Arabidopsis root sieve element markers at 24h of iron deficiency</name><description>RNA-seq of pPEAR1::dBOX-YFP, pPEAR1-erGFP, and pC2-YFP to characterize the transcriptome associated with progressively more differentiated sieve elements. pPEAR1::dBOX-YFP is the proxy for early / phloem initials. pPEAR1-erGFP is the proxy for transit amplifying protophloem. pC2-YFP is the proxy for differentiation sieve elements. Each marker line was grown for 4 days in standard MS (Murashige &amp; Skoog) media then transferred to iron deficient media (Murashige &amp; Skoog containing ferrozine to chelate any iron present so that it's biounavailable). At 24h after transfer, roots were protoplasted and sorted using Fluorescence Activated Cell Sorting (FACS) to isolate GFP-positive or YFP-positive cells. Then, RNA-seq was performed in the sorted cell populations.</description><dates><release>2025-11-21T00:00:00Z</release><modification>2026-05-30T16:35:21.147Z</modification><creation>2025-10-13T15:18:05.76Z</creation></dates><accession>E-MTAB-15703</accession><cross_references><ENA>ERP182061</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><EFO>EFO_0003969</EFO></cross_references></HashMap>