Reine U Protacio
This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.
Staff Scientist
Also affiliated: Northwestern University (1996–1997); Harvard University (2002–2004)
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Reine U. Protacio's research focuses on understanding the molecular mechanisms that govern genetic recombination, particularly during meiosis. Her work investigates how environmental factors and specific DNA sequences influence the landscape of meiotic recombination, with implications for evolutionary processes. Protacio also studies the function of helicase enzymes, such as Pif1, examining their roles in DNA unwinding, DNA repair, and mitochondrial function. Her recent publications explore the impact of CRISPR/Cas9 gene editing efficiency in yeast and address practical laboratory challenges related to yeast cell culture. Protacio collaborates with researchers at the University of Arkansas for Medical Sciences, including Wayne P. Wahls, Emory G. Malone, and Kevin D. Raney, with whom she has co-authored multiple publications. Her scholarship metrics include an h-index of 10 and 719 total citations across 17 publications.
Metrics
- h-index: 11
- Publications: 25
- Citations: 773
Positions
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Staff Scientist publications 2013–2025University of Arkansas for Medical Sciences Institution web page
Selected Publications
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Long multiply marked DNA repair template reveals lengths and fidelity of genome editing tracts in Schizosaccharomyces pombe (2025)
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Targeted Forward Genetics: Saturating Mutational Analyses of Specific Target Loci Within the Genome (2024)
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Agar lot-specific inhibition in the plating efficiency of yeast spores and cells (2024)
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Creating Meiotic Recombination-Regulating DNA Sites by SpEDIT in Fission Yeast Reveals Inefficiencies, Target-Site Duplications, and Ectopic Insertions (2024)
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Distance-dependent effects on CRISPR/Cas9-mediated genome editing in Schizosaccharomyces pombe compromise efficiency and create unsought alleles (2024)
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Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge (2024)
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Laboratory horror stories: Poison in the agars (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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DNA sequences and distinct mechanisms for ura4-595 and ura4-294 alleles of S. pombe (2024)
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Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution (2022)
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Primary acute lymphoblastic leukemia cells are susceptible to microtubule depolymerization in G1 and M phases through distinct cell death pathways (2022)
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Molecular mechanisms for environmentally induced and evolutionarily rapid redistribution (plasticity) of meiotic recombination (2021)
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Molecular mechanisms for environmentally induced plasticity in the positioning of meiotic recombination at hotspots (2020)
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Targeted Forward Genetics: Population-Scale Analyses of Allele Replacements Spanning Thousands of Base Pairs in Fission Yeast (2019)
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Diverse DNA Sequence Motifs Activate Meiotic Recombination Hotspots Through a Common Chromatin Remodeling Pathway (2019)
Collaboration Network
Top Collaborators
- Rapid, efficient and precise allele replacement in the fission yeast Schizosaccharomyces pombe
- Chromatin-mediated regulators of meiotic recombination revealed by proteomics of a recombination hotspot
- Molecular mechanisms for environmentally induced and evolutionarily rapid redistribution (plasticity) of meiotic recombination
- Diverse DNA Sequence Motifs Activate Meiotic Recombination Hotspots Through a Common Chromatin Remodeling Pathway
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
Showing 5 of 20 shared publications
- Rapid, efficient and precise allele replacement in the fission yeast Schizosaccharomyces pombe
- Chromatin-mediated regulators of meiotic recombination revealed by proteomics of a recombination hotspot
- Molecular mechanisms for environmentally induced and evolutionarily rapid redistribution (plasticity) of meiotic recombination
- Diverse DNA Sequence Motifs Activate Meiotic Recombination Hotspots Through a Common Chromatin Remodeling Pathway
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
Showing 5 of 14 shared publications
- Rapid, efficient and precise allele replacement in the fission yeast Schizosaccharomyces pombe
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
- 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
- A stress‐activated, p38 MAPK‐ATF/CREB pathway regulates the post‐transcriptional decay of target mRNAs
- Rapid, efficient and precise allele replacement in the fission yeast Schizosaccharomyces pombe
- Chromatin-mediated regulators of meiotic recombination revealed by proteomics of a recombination hotspot
- Targeted Forward Genetics: Population-Scale Analyses of Allele Replacements Spanning Thousands of Base Pairs in Fission Yeast
- Nonsense codon suppression in fission yeast due to mutations of tRNASer.11 and translation release factor Sup35 (eRF3)
- Proteomic analysis of a meiotic recombination hotspot
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- Distance-dependent effects on CRISPR/Cas9-mediated genome editing in Schizosaccharomyces pombe compromise efficiency and create unsought alleles
- Agar lot-specific inhibition in the plating efficiency of yeast spores and cells
- DNA sequences and distinct mechanisms for ura4-595 and ura4-294 alleles of S. pombe
- Rapid, efficient and precise allele replacement in the fission yeast Schizosaccharomyces pombe
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
- A stress‐activated, p38 MAPK‐ATF/CREB pathway regulates the post‐transcriptional decay of target mRNAs
- Molecular mechanisms for environmentally induced and evolutionarily rapid redistribution (plasticity) of meiotic recombination
- Diverse DNA Sequence Motifs Activate Meiotic Recombination Hotspots Through a Common Chromatin Remodeling Pathway
- Molecular mechanisms for environmentally induced plasticity in the positioning of meiotic recombination at hotspots
- Eukaryotic Pif1 helicase unwinds G-quadruplex and dsDNA using a conserved wedge
- Primary acute lymphoblastic leukemia cells are susceptible to microtubule depolymerization in G1 and M phases through distinct cell death pathways
- Two residues in the DNA binding site of Pif1 helicase are essential for nuclear functions but dispensable for mitochondrial respiratory growth
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
- A stress‐activated, p38 MAPK‐ATF/CREB pathway regulates the post‐transcriptional decay of target mRNAs
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
- A stress‐activated, p38 MAPK‐ATF/CREB pathway regulates the post‐transcriptional decay of target mRNAs
- A Stress-Activated, p38 Mitogen-Activated Protein Kinase–ATF/CREB Pathway Regulates Posttranscriptional, Sequence-Dependent Decay of Target RNAs
- A stress‐activated, p38 MAPK‐ATF/CREB pathway regulates the post‐transcriptional decay of target mRNAs
- Chromatin-mediated regulators of meiotic recombination revealed by proteomics of a recombination hotspot
- Targeted Forward Genetics: Population-Scale Analyses of Allele Replacements Spanning Thousands of Base Pairs in Fission Yeast
- Chromatin-mediated regulators of meiotic recombination revealed by proteomics of a recombination hotspot
- Proteomic analysis of a meiotic recombination hotspot
- 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
- 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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