Alicia K. Byrd
Assistant Professor
Also affiliated: Pennsylvania State University (2002); Vanderbilt University (2002); University of Arkansas Medical Center (2022–2024); Jacksonville University (2015); Winthrop Rockefeller Foundation (2020–2025); Arkansas Department of Agriculture (2014)
Faculty Researcher
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Alicia K. Byrd's research focuses on the function and regulation of DNA helicases, particularly the Pif1 family, at replication forks and in the context of G-quadruplex structures. Her work investigates how these enzymes interact with DNA and viral proteins, impacting processes such as DNA unwinding and the remodeling of protein-nucleic acid complexes. She has published on the role of Pif1 helicase in processes involving Sub1 and Cdc13, and on the interaction between bacteriophage T4 DNA processing proteins gp32 and Dda.
Further research by Byrd explores the role of G-quadruplexes in biological processes, including their influence on helicase activity and liquid-liquid phase separation. Her work also extends to the Hepatitis C virus, examining how its nonstructural protein NS3 interacts with viral G-quadruplex RNA. Byrd also investigates methodological aspects of molecular biology techniques, such as the impact of untargeted CUT&Tag reads on G-quadruplex identification. Her scholarship metrics include an h-index of 27, 1,925 total citations across 57 publications, and she is recognized as a highly cited researcher. She leads a research group and collaborates with researchers at the University of Arkansas for Medical Sciences and the University of Arkansas at Fayetteville.
Metrics
- h-index: 27
- Publications: 57
- Citations: 1,948
Selected Publications
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Response to the commentary by Melidis <i>et al.</i> on “Untargeted CUT&Tag reads are enriched at accessible chromatin and restrict identification of potential G4-forming sequences in G4-targeted CUT&Tag experiments” (2025)
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Untargeted CUT&Tag reads are enriched at accessible chromatin and restrict identification of potential G4-forming sequences in G4-targeted CUT&Tag experiments (2025)
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Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB (2025)
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Structural and functional insights into the interaction between the bacteriophage T4 DNA processing proteins gp32 and Dda (2024)
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Untargeted CUT&Tag and BG4 CUT&Tag are both enriched at G-quadruplexes and accessible chromatin (2024)
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Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge (2024)
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Two residues in the DNA binding site of Pif1 helicase are essential for nuclear functions but dispensable for mitochondrial respiratory growth (2024)
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Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB (2024)
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Pif1 Helicase Mediates Remodeling of Protein-Nucleic Acid Complexes by Promoting Dissociation of Sub1 from G-Quadruplex DNA and Cdc13 from G-Rich Single-Stranded DNA (2023)
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Hepatitis C virus nonstructural protein NS3 unfolds viral G-quadruplex RNA structures (2022)
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Alignment of helicases on single-stranded DNA increases activity (2022)
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Role and Regulation of Pif1 Family Helicases at the Replication Fork (2022)
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Monitoring helicase-catalyzed unwinding of multiple duplexes simultaneously (2022)
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A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp> (2021)
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G-quadruplex DNA inhibits unwinding activity but promotes liquid–liquid phase separation by the DEAD-box helicase Ded1p (2021)
Grants & Funding
As listed on this researcher's institutional profile.
- Role of HELB in the Replication Stress Response NIH/NIGMS
- The effect of rs75770066, a stroke associated single nucleotide polymorphism, on enzyme activity UAMS Internal Research Awards
- Seeds of Science Pilot award UAMS Internal Research Awards
- DNA Helicases: Mechanism and Function NIH
- Functions and Mechanisms of Helicases and G-Quadruplex Nucleic Acids NIH
- The Role of DNA Helicase B in Response to DNA Replication Stress UAMS Internal Research Awards
- Measurement of Helicase Diffusion and Cooperativity at the Single Molecule Level Burroughs Wellcome Fund
- Identification of synthetic lethal targets for treating breast cancer Arkansas Breast Cancer Research Program
- Role of HELB in the Replication Stress Response
Collaboration Network
Top Collaborators
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- Role and Regulation of Pif1 Family Helicases at the Replication Fork
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Untargeted CUT&Tag reads are enriched at accessible chromatin and restrict identification of potential G4-forming sequences in G4-targeted CUT&Tag experiments
- Untargeted CUT&Tag and BG4 CUT&Tag are both enriched at G-quadruplexes and accessible chromatin
Showing 5 of 9 shared publications
- G-quadruplex DNA inhibits unwinding activity but promotes liquid–liquid phase separation by the DEAD-box helicase Ded1p
- Hepatitis C virus nonstructural protein NS3 unfolds viral G-quadruplex RNA structures
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Pif1 Helicase Mediates Remodeling of Protein-Nucleic Acid Complexes by Promoting Dissociation of Sub1 from G-Quadruplex DNA and Cdc13 from G-Rich Single-Stranded DNA
Showing 5 of 6 shared publications
- G-quadruplex DNA inhibits unwinding activity but promotes liquid–liquid phase separation by the DEAD-box helicase Ded1p
- Hepatitis C virus nonstructural protein NS3 unfolds viral G-quadruplex RNA structures
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Pif1 Helicase Mediates Remodeling of Protein-Nucleic Acid Complexes by Promoting Dissociation of Sub1 from G-Quadruplex DNA and Cdc13 from G-Rich Single-Stranded DNA
Showing 5 of 6 shared publications
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- G-quadruplex DNA inhibits unwinding activity but promotes liquid–liquid phase separation by the DEAD-box helicase Ded1p
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Two residues in the DNA binding site of Pif1 helicase are essential for nuclear functions but dispensable for mitochondrial respiratory growth
- Role and Regulation of Pif1 Family Helicases at the Replication Fork
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Monitoring helicase-catalyzed unwinding of multiple duplexes simultaneously
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Multi-omics data integration reveals correlated regulatory features of triple negative breast cancer
- A structural feature of Dda helicase which enhances displacement of streptavidin and <i>trp</i> repressor from <scp>DNA</scp>
- Pif1 Helicase Mediates Remodeling of Protein-Nucleic Acid Complexes by Promoting Dissociation of Sub1 from G-Quadruplex DNA and Cdc13 from G-Rich Single-Stranded DNA
- Two residues in the DNA binding site of Pif1 helicase are essential for nuclear functions but dispensable for mitochondrial respiratory growth
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Rare SNP in the <i>HELB</i> gene interferes with RPA interaction and cellular function of HELB
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- Two residues in the DNA binding site of Pif1 helicase are essential for nuclear functions but dispensable for mitochondrial respiratory growth
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