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Series GSE143857 Query DataSets for GSE143857
Status Public on Feb 04, 2020
Title Deregulated overexpression of the high affinity Cu transporter COPT1 alters iron homeostasis in Arabidopsis
Organism Arabidopsis thaliana
Experiment type Expression profiling by array
Summary The present work describes the effects on iron homeostasis when copper transport was deregulated in Arabidopsis thaliana by overexpressing copper transporters (COPTOE). A genome-wide analysis conducted on COPT1OE plants, highlighted that iron homeostasis gene expression was affected, both under copper deficiency and excess. Among the inhibited genes were those encoding the iron uptake machinery and their transcriptional regulators. Subsequently, COPTOE seedlings contained less iron and were more sensitive than controls to iron deficiency. These results emphasized the importance of appropriate spatiotemporal copper uptake for iron homeostasis under copper deficiency. The deregulation of copper-I uptake difficulted the transcriptional activation of the subgroup Ib of basic helix-loop-helix (bHLH-Ib) factors. Oppositely, copper excess inhibited the expression of the master regulator FIT but activate bHLH-Ib expression in COPTOE plants, in both cases leading to the lack of an adequate iron uptake response. As copper increased in the media, iron-III was accumulated in roots, accounting for a defective iron mobilization to the aerial parts, and this effect was exacerbated in COPTOE plants. Thus, iron-III overloading in roots inhibited local iron deficiency responses, aimed to metal uptake from soil, leading to a general lower iron content in the COPTOE seedlings. The understanding of the role of copper uptake in iron metabolism could be applied for increasing crops resistance to iron deficiency
 
Overall design At least three biological replicates of Arabidopsis seedlings were generated for 2 genotypes, Col-0 and COPT1 overexpressor line (COPT1 OE); and 2 growth condictions; first one with a cupper deficient medium (Cu Def, 0 μM CuSO4) and a second one with a cupper excess medium (Cu Exc, 10 μM CuSO4). For each growth condition, COPT1 OE versus Col-0 samples were compared; in each comparasion at least three biological replicates were made, two replicas were labeled with Cy5 for the COPT1 OE and Cy3 for the Col-0 sample, while the other replicas were reversed-labeled.
 
Contributor(s) Perea-García A, Andrés-Bordería A, Vera-Sirera F, Pérez-Amador MA, Puig S, Peñarrubia L
Citation(s) 32793263
Submission date Jan 17, 2020
Last update date Aug 24, 2020
Contact name Francisco Vera-Sirera
E-mail(s) [email protected]
Organization name IBMCP (UPV-CSIC)
Lab Lab 2.08
Street address Ingeniero Fausto Elio, s/n
City Valencia
ZIP/Postal code 46022
Country Spain
 
Platforms (1)
GPL2508 Galbraith Laboratory Operon Long Oligonucleotide Microarray version 3.0 (ATv302.02.Z)
Samples (7)
GSM4275474 COPT1 over expressor line versus Col-0 grown in MS without cupper replicate 1
GSM4275475 COPT1 over expressor line versus Col-0 grown in MS without cupper replicate 2
GSM4275476 COPT1 over expressor line versus Col-0 grown in MS without cupper replicate 3
Relations
BioProject PRJNA601916

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE143857_RAW.tar 19.2 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table

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