Zebrafish Polymerase Theta and human Polymerase Theta: Orthologues with homologous function

DNA Polymerase Theta (Pol θ) is a conserved an A-family polymerase that plays an essential role in repairing double strand breaks, through micro-homology end joining, and bypassing DNA lesions, through translesion synthesis, to protect genome integrity. Despite its essential role in DNA repair, Pol θ is inherently error-prone. Recently, key loop regions were identified to play an important role in key functions of Pol θ. Here we present a comparative structure-function study of the polymerase domain of zebrafish and human Pol θ. We show that these two proteins share a large amount of sequence and structural homology. Using a classical biochemical approach we observe that zebrafish Pol θ displays behavior characteristic of human Pol θ, including DNA template extension in the presence of different divalent metals, microhomology-mediated end joining, and translesion synthesis. These results will support future studies looking to gain insight into Pol θ function on the basis of evolutionarily conserved features.

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Publication Details

Journal
PLoS ONE
Published
2025-04-29
DOI
https://doi.org/10.1371/journal.pone.0321886
Citations
2
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
1.61

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article

Zebrafish Polymerase Theta and human Polymerase Theta: Orthologues with homologous function

Jamie B. Towle-Weicksel, Steven E. Weicksel, Sydney Green, Isaiah R Schmidtke et al.
2 citations
PLoS ONE
DNA Repair Mechanisms
1.61
article

Zebrafish Polymerase Theta and human Polymerase Theta: Orthologues with homologous function

Jamie B. Towle-Weicksel, Steven E. Weicksel, Sydney Green, Isaiah R Schmidtke, Lily Kimball, Ivy Par, Sophia Schobel, Yayleene Palacio, Corey Thomas, Makayla Griffin, L Rothwell
article en
2 citations

Abstract

DNA Polymerase Theta (Pol θ) is a conserved an A-family polymerase that plays an essential role in repairing double strand breaks, through micro-homology end joining, and bypassing DNA lesions, through translesion synthesis, to protect genome integrity. Despite its essential role in DNA repair, Pol θ is inherently error-prone. Recently, key loop regions were identified to play an important role in key functions of Pol θ. Here we present a comparative structure-function study of the polymerase domain of zebrafish and human Pol θ. We show that these two proteins share a large amount of sequence and structural homology. Using a classical biochemical approach we observe that zebrafish Pol θ displays behavior characteristic of human Pol θ, including DNA template extension in the presence of different divalent metals, microhomology-mediated end joining, and translesion synthesis. These results will support future studies looking to gain insight into Pol θ function on the basis of evolutionarily conserved features.

PLoS ONEVol. 20(4)
Bryant University (US), Rhode Island College (US)
National Institute of General Medical Sciences
Openalex Percentile: Top 18%
DNA Repair Mechanisms
1.61
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Zebrafish Polymerase Theta and human Polymerase Theta: Orthologues with homologous function — Jamie B. Towle-Weicksel, Steven E. Weicksel, et al. · PLoS ONE (2025) | TGRS Research Map | TGRS