Huntington’s disease LIG1 modifier variant increases ligase fidelity and suppresses somatic CAG repeat expansion

Huntington's disease (HD) is a fatal neurodegenerative disorder caused by inheriting an expanded CAG repeat tract in the huntingtin gene (<i>HTT</i>) that further expands in somatic cells over an individual's lifetime. Genome-wide association studies have provided critical insight into factors that modify the course of disease. These include DNA repair genes that alter the rate of somatic expansion and other genes that do not appear to directly influence this process. One modifier gene is DNA ligase 1 (<i>LIG1</i>), in which a variant specifying a lysine to asparagine substitution (K845N) is associated with a profound (7 to 8 y) delay in the onset of motor signs. Here, we have taken a multifaceted approach to gain insight into the protective nature of this variant in HD. We demonstrate using in vitro ligase assays and enzyme kinetics that K845N enhances discrimination toward mismatched substrates and increases repair fidelity. Consistent with increased ligation fidelity, K845N confers protection against oxidative stress in cell-based assays. Finally, we demonstrate that the mouse LIG1 K843N orthologue suppresses somatic CAG expansion in HD knock-in mice. Overall, our data provide evidence that altered LIG1 function due to the K845N substitution may contribute to HD clinical delay by slowing somatic expansion in the brain and protecting the genome globally against damage. Significantly, our results provide a mechanistic foundation for considering DNA ligase fidelity as a therapeutic target in HD and potentially in other trinucleotide repeat disorders.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-03-02
DOI
https://doi.org/10.1073/pnas.2518854123
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Huntington’s disease LIG1 modifier variant increases ligase fidelity and suppresses somatic CAG repeat expansion

Marissa A Andrew, Mouro Pinto Ricardo, Andrew Jiang, David H. Beier et al.
Proceedings of the National Academy of Sciences
Genetic Neurodegenerative Diseases
article

Huntington’s disease LIG1 modifier variant increases ligase fidelity and suppresses somatic CAG repeat expansion

Marissa A Andrew, Mouro Pinto Ricardo, Andrew Jiang, David H. Beier, Marina Kovalenko, Patrick O’Brien, I. Sik Seong, Ramee Lee, Wonju Kim, Ryan Murtha, Eliza Lee, Seung Kwak, Bhairavi Srinageshwar, Brigitte Demelo, Esaria Oliver, Diane Lucente, Marcy E. MacDonald, Jayla Ruliera, James F. Gusella, Vanessa C. Wheeler, Faaiza Saif, Yejin Lee, Tammy Gillis
article en

Abstract

Huntington's disease (HD) is a fatal neurodegenerative disorder caused by inheriting an expanded CAG repeat tract in the huntingtin gene (<i>HTT</i>) that further expands in somatic cells over an individual's lifetime. Genome-wide association studies have provided critical insight into factors that modify the course of disease. These include DNA repair genes that alter the rate of somatic expansion and other genes that do not appear to directly influence this process. One modifier gene is DNA ligase 1 (<i>LIG1</i>), in which a variant specifying a lysine to asparagine substitution (K845N) is associated with a profound (7 to 8 y) delay in the onset of motor signs. Here, we have taken a multifaceted approach to gain insight into the protective nature of this variant in HD. We demonstrate using in vitro ligase assays and enzyme kinetics that K845N enhances discrimination toward mismatched substrates and increases repair fidelity. Consistent with increased ligation fidelity, K845N confers protection against oxidative stress in cell-based assays. Finally, we demonstrate that the mouse LIG1 K843N orthologue suppresses somatic CAG expansion in HD knock-in mice. Overall, our data provide evidence that altered LIG1 function due to the K845N substitution may contribute to HD clinical delay by slowing somatic expansion in the brain and protecting the genome globally against damage. Significantly, our results provide a mechanistic foundation for considering DNA ligase fidelity as a therapeutic target in HD and potentially in other trinucleotide repeat disorders.

Proceedings of the National Academy of SciencesVol. 123(10)
Broad Institute (US), Harvard University (US), University of Michigan (US), CHDI Foundation (US), Massachusetts General Hospital (US), Boston VA Research Institute (US)
National Science Foundation, Pfizer, CHDI Foundation, National Institutes of Health
Reduced inequalities, Peace, Justice and strong institutions
Openalex Percentile: Top 38%
Genetic Neurodegenerative Diseases
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