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Initiation and regulation of iron economy in Arabidopsis thaliana chloroplasts

dc.contributor.authorKroh, Gretchen Elizabeth, author
dc.contributor.authorPilon, Marinus, advisor
dc.contributor.authorReddy, Anireddy, committee member
dc.contributor.authorBush, Daniel, committee member
dc.contributor.authorBedinger, Patricia, committee member
dc.contributor.authorArgueso, Cristiana, committee member
dc.date.accessioned2020-08-31T10:11:47Z
dc.date.available2021-06-15T10:11:47Z
dc.date.issued2020
dc.descriptionZip file contains supplementary table.
dc.description.abstractIron (Fe) is biologically important for all organisms because of its role as a protein cofactor which provides redox and catalytic functions. Fe cofactors come in 3 different forms (Fe-S clusters, heme, and non-heme Fe). Plants have a stronger requirement for Fe than non-photosynthetic organisms because the chloroplast has a high demand for Fe. Plants are commonly Fe deficient because soil Fe is typically found in the non-bioavailable, ferric (Fe3+) form, which limits plant growth in natural and agricultural settings. When grown on soils where Fe availability is low, plants can increase Fe uptake and use Fe more efficiently. The leaf response to Fe limitation in the model plant, Arabidopsis thaliana, is the topic of my dissertation. As a major contribution to a larger study, I first characterized the transcriptional response for specific leaf genes to Fe deficiency in the leaf and found that transcripts for abundant chloroplast Fe proteins were down-regulated, suggesting an Fe economy response. Specifically, photosynthetic electron transport and chloroplast Fe-S assembly were targeted for down-regulation. Fe deficiency affects photosynthesis and chloroplast Fe protein expression. I characterized a photosynthesis mutant and found that the regulation of Fe protein expression is maintained, suggesting that loss of electron transport does not trigger down-regulation of Fe protein expression. By using RNA-seq, I analyzed genome-wide transcriptomic changes to identify co-regulated transcripts early in the Fe economy response, including candidate transcription factors. The transcriptional responses in wild type Fe limited plants and a chloroplast Fe-S assembly mutant were independent of each other, suggesting that Fe-S assembly does not generate a signal to regulate chloroplast Fe proteins. The novel insights provided in this dissertation form a foundation for understanding how photosynthetic organisms cope with Fe limitation. From an applied perspective, the results of this dissertation open new avenues to minimize effects of Fe deficiency in agricultural settings.
dc.format.mediumborn digital
dc.format.mediumdoctoral dissertations
dc.format.mediumZIP
dc.format.mediumPDF
dc.identifierKroh_colostate_0053A_15986.pdf
dc.identifier.urihttps://hdl.handle.net/10217/211762
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2020-
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectFe-S cluster
dc.subjectiron homeostasis
dc.subjectchloroplast
dc.subjectphotosynthesis
dc.subjectFerredoxin
dc.titleInitiation and regulation of iron economy in Arabidopsis thaliana chloroplasts
dc.typeText
dcterms.embargo.expires2021-06-15
dcterms.embargo.terms2021-06-15
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineBiology
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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