Identification and characterization of a heme responsive element in the hrg-1 promoter
dc.contributor.advisor | Hamza, Iqbal | en_US |
dc.contributor.author | Sinclair, Jason | en_US |
dc.contributor.department | Animal Sciences | en_US |
dc.contributor.publisher | Digital Repository at the University of Maryland | en_US |
dc.contributor.publisher | University of Maryland (College Park, Md.) | en_US |
dc.date.accessioned | 2010-01-16T06:32:43Z | |
dc.date.available | 2010-01-16T06:32:43Z | |
dc.date.issued | 2008 | en_US |
dc.description.abstract | Despite its biological significance, little is known about how animals sense and respond to heme to maintain homeostasis. C. elegans is a heme auxotroph, which makes it an excellent model to identify and dissect heme homeostasis pathways. Using C. elegans we have identified HRG-1, a vesicular heme transporter that is transcriptionally upregulated when environmental heme is low. The current study seeks to address how hrg-1 is regulated by heme. Here, we show that a putative 23 base pair (bp) heme-responsive element (HRE) and GATA-binding motifs are necessary for heme-dependent regulation of hrg-1. The HRE comprises both enhancer and repressor elements and works in conjunction with ELT-2 to regulate hrg-1 expression. We propose that the HRE could be used as a molecular tool in C. elegans to tightly regulate internal gene expression by modulating environmental heme. Our ultimate goal is to identify the trans-acting factor to eventually create a whole animal sensor for monitoring organismal heme homeostasis. | en_US |
dc.identifier.uri | http://hdl.handle.net/1903/9798 | |
dc.subject.pqcontrolled | Biology, Molecular | en_US |
dc.subject.pqcontrolled | Biology, Cell | en_US |
dc.subject.pquncontrolled | c. elegans | en_US |
dc.subject.pquncontrolled | heme | en_US |
dc.subject.pquncontrolled | transcription | en_US |
dc.title | Identification and characterization of a heme responsive element in the hrg-1 promoter | en_US |
dc.type | Thesis | en_US |
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