DELINEATING THE ROLES OF C. ELEGANS HEME RESPONSIVE GENES HRG-2 AND HRG-3 IN HEME HOMEOSTASIS

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dc.contributor.advisorHamza, Iqbalen_US
dc.contributor.authorChen, Caiyongen_US
dc.contributor.departmentAnimal Sciencesen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2010-02-19T07:03:21Z
dc.date.available2010-02-19T07:03:21Z
dc.date.issued2009en_US
dc.description.abstractHeme is an essential cofactor for diverse biological processes such as oxygen transport, xenobiotic detoxification, and circadian clock control. Since free heme is hydrophobic and cytotoxic, we hypothesize that within eukaryotic cells, specific trafficking pathways exist for the delivery of heme to different subcellular destinations where hemoproteins reside. To identify molecules that may be involved in heme homeostasis, we conducted a <italic>C. elegans </italic>microarray experiment on RNA extracted from worms grown at different concentrations of heme in axenic liquid medium. Analysis of the microarrays revealed that the mRNA levels of <italic>heme-responsive gene-2 (hrg-2)</italic> and <italic>hrg-3</italic> increased more than 70 fold when worms were grown at 4 µM compared to 20 µM heme. <italic>hrg-2</italic> is expressed in hypodermal tissues in the worm, and the protein localizes to the endoplasmic reticulum and the apical plasma membrane. <italic>In vitro</italic> hemin agarose pull-down experiments indicate that HRG-2 binds heme. Deletion of <italic>hrg-2</italic> in <italic>C. elegans</italic> leads to reduced growth rate at low heme. Moreover, expression of HRG-2 in <italic>hem1&delta;</italic>, a heme-deficient yeast strain, results in growth rescue at submicromolar concentrations of exogenous heme. These results indicate that HRG-2 may either directly participate in heme uptake or facilitate heme delivery to another protein. Unlike <italic>hrg-2</italic>, <italic>hrg-3</italic> is exclusively expressed in the worm intestine under heme deficiency. Following its synthesis, HRG-3 is secreted into the body cavity pseudocoelom. Deletion of <italic>hrg-3</italic> results in increased heme levels in the worm intestine, suggesting that HRG-3 may function in intercellular heme transport in <italic>C. elegans</italic>. To identify the functional network or pathways for HRG-2 and HRG-3, we performed a genome-wide microarray analysis using RNA samples prepared from the worms grown at different concentrations of heme and oxygen. The results showed that a total of 446 genes were transcriptionally altered by heme and/or oxygen. Among them, 41 and 29 genes exhibited similar expression profiles to <italic>hrg-2</italic> and <italic>hrg-3</italic>, respectively. We postulate that these genes may function in conjunction with <italic>hrg-2</italic> and <italic>hrg-3</italic>. Taken together, we have identified two novel heme-responsive genes in metazoa that may play critical roles in modulating organismal heme homeostasis in <italic>C. elegans</italic>.en_US
dc.identifier.urihttp://hdl.handle.net/1903/9977
dc.subject.pqcontrolledBiology, Molecularen_US
dc.subject.pqcontrolledBiology, Geneticsen_US
dc.subject.pquncontrolledhelminthen_US
dc.subject.pquncontrolledhemeen_US
dc.subject.pquncontrolledmetalsen_US
dc.subject.pquncontrolledmicroarrayen_US
dc.subject.pquncontrollednematodeen_US
dc.subject.pquncontrolledtetrapyrroleen_US
dc.titleDELINEATING THE ROLES OF C. ELEGANS HEME RESPONSIVE GENES HRG-2 AND HRG-3 IN HEME HOMEOSTASISen_US
dc.typeDissertationen_US

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