<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T17:51:22Z</responseDate><request verb="GetRecord" identifier="oai:wakespace.lib.wfu.edu:10339/39141" metadataPrefix="dim">https://wakespace.lib.wfu.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:null:10339/39141</identifier><datestamp>2026-09-02T12:29:55Z</datestamp><setSpec>com_10339_14934</setSpec><setSpec>col_10339_38132</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Smaldino, Phillip James</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2014-01-15T09:35:36Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2014-07-15T08:30:09Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2013</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://wakespace.lib.wfu.edu/handle/10339/39141</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">G-quadruplexes (G4s) are four-stranded structures formed by guanine-rich DNA or RNA sequences in which the strands can be orientated in parallel, antiparallel, or mixed parallel/antiparallel orientations. It has been previously shown that the DHX36 gene product, G4-Resolvase1 (G4R1), binds parallel tetramolecular G4-DNA with high affinity and resolves these structures into single strands. Here we show that G4R1 specifically binds to a parallel, unimolecular G4-DNA with remarkable affinity, with Kd values in the low pM range; the tightest reported binding affinity for any known G4-binding protein. Using a novel peptide nucleic acid (PNA) trap assay, we show that G4R1 catalyzes unwinding of unimolecular G4-DNA into an unstructured state. Additionally, we provide strong evidence for the presence of unimolecular G4-structures in the promoter of the Yin Yang 1 (YY1) gene and demonstrate that these structures have an inhibitory effect on reporter assay expression. We also discovered that G4R1 directly binds and unwinds G4-structures in the YY1 promoter, subsequently enhancing reporter expression. Consistently, ectopically expressed G4R1 increased endogenous YY1 levels and gene array analysis consisting of 258 patient breast cancer samples indicated a significant, positive correlation between G4R1 and YY1 expression. We went on to demonstrate that G4R1 tightly binds to mixed parallel/antiparallel and antiparallel unimolecular telomeric G4-DNA.  Furthermore, we show specific requirements of G4R1 for tight binding to telomeric DNA which are: 1) presence of G4-structure in the sequence and 2) a guanine-containing 3&amp;apos;-tail. Overall findings from this dissertation strongly suggest that G4R1 tightly and specifically binds to an exceptional array of G4-structures and could potentially serve as a &amp;quot;pan&amp;quot; G4-resolver in the cell. Indeed this finding could have significant genomic impact, as &amp;gt;375,000 G4-forming motifs exist in the genome and G4-structures have been shown to play prominent regulatory roles in transcription, translation, replication, immunoglobin switching, and telomere biology.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">en</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Wake Forest University</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">dhx36</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">G4 Resolvase 1</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">G-quadruplex</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">quadruplex</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">RHAU</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Telomere</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">G4-RESOLVASE 1 TIGHTLY BINDS AND CATALYTICALLY UNWINDS UNIMOLECULAR G-QUADRUPLEX STRUCTURES WITH IMPLICATIONS FOR GENE TRANSCRIPTION AND TELOMERE BIOLOGY</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Dissertation</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeChair" lang="en_US">Akman, Steven A</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Akman, Steven A</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Vaughn, James P</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Hollis, Thomas</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Scarpinato, Karin D</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Sui, Guangchao</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Wang, Yuh-Hwa</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="discipline" lang="en_US">Cancer Biology</dim:field>
   <dim:field mdschema="thesis" element="embargo" qualifier="terms" lang="en_US">2014-7-15</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
</dim:dim>
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