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Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress
Telomeres consist of special features and proteins to protect the ends of each chromosome from deterioration and fusion. The telomeric DNA repeats are highly susceptible to oxidative damage that can accelerate telomere shortening and affect telomere integrity. Several DNA repair factors including MY...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267527/ https://www.ncbi.nlm.nih.gov/pubmed/35812693 http://dx.doi.org/10.21926/obm.geriatr.2202196 |
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author | Gupta, Aditi Hwang, Bor-Jang Benyamien-Roufaeil, Daniel Jain, Sara Liu, Sophie Gonzales, Rex Brown, Robert A. Zalzman, Michal Lu, A-Lien |
author_facet | Gupta, Aditi Hwang, Bor-Jang Benyamien-Roufaeil, Daniel Jain, Sara Liu, Sophie Gonzales, Rex Brown, Robert A. Zalzman, Michal Lu, A-Lien |
author_sort | Gupta, Aditi |
collection | PubMed |
description | Telomeres consist of special features and proteins to protect the ends of each chromosome from deterioration and fusion. The telomeric DNA repeats are highly susceptible to oxidative damage that can accelerate telomere shortening and affect telomere integrity. Several DNA repair factors including MYH/MUTYH DNA glycosylase, its interacting partners Rad9/Rad1/Hus1 checkpoint clamp, and SIRT6 aging regulator, are associated with the telomeres. MYH prevents C:G to A:T mutation by removing adenine mispaired with a frequent oxidative DNA lesion, 8-oxoguanine. Here, we show that hMYH knockout (KO) human HEK-293T cells are more sensitive to H(2)O(2) treatment, have higher levels of DNA strand breaks and shorter telomeres than the control hMYH(+/+) cells. SIRT6 foci increase at both the global genome and at telomeric regions in H(2)O(2)-treated hMYH(+/+) cells. However, in untreated hMYH KO HEK-293T cells, SIRT6 foci only increase at the global genome, but not at the telomeric regions. In addition, the hMYH KO HEK-293T cells have increased extra-chromosomal and intra-chromosomal telomeres compared to the control cells, even in the absence of H(2)O(2) treatment. After H(2)O(2) treatment, the frequency of extra-chromosomal telomeres increased in control HEK-293T cells. Remarkably, in H(2)O(2)-treated hMYH KO cells, the frequencies of extra-chromosomal telomeres, intra-chromosomal telomeres, and telomere fusions are further increased. We further found that the sensitivity to H(2)O(2) and shortened telomeres of hMYH KO cells, are restored by expressing wild-type hMYH, and partially rescued by expressing hMYH(Q324H) mutant (defective in Hus1 interaction only), but not by expressing hMYH(V315A) mutant (defective in both SIRT6 and Hus1 interactions). Thus, MYH interactions with SIRT6 and Hus1 are critical for maintaining cell viability and telomeric stability. Therefore, the failure to coordinate 8-oxoG repair is detrimental to telomere integrity. |
format | Online Article Text |
id | pubmed-9267527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-92675272022-07-08 Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress Gupta, Aditi Hwang, Bor-Jang Benyamien-Roufaeil, Daniel Jain, Sara Liu, Sophie Gonzales, Rex Brown, Robert A. Zalzman, Michal Lu, A-Lien OBM Geriat Article Telomeres consist of special features and proteins to protect the ends of each chromosome from deterioration and fusion. The telomeric DNA repeats are highly susceptible to oxidative damage that can accelerate telomere shortening and affect telomere integrity. Several DNA repair factors including MYH/MUTYH DNA glycosylase, its interacting partners Rad9/Rad1/Hus1 checkpoint clamp, and SIRT6 aging regulator, are associated with the telomeres. MYH prevents C:G to A:T mutation by removing adenine mispaired with a frequent oxidative DNA lesion, 8-oxoguanine. Here, we show that hMYH knockout (KO) human HEK-293T cells are more sensitive to H(2)O(2) treatment, have higher levels of DNA strand breaks and shorter telomeres than the control hMYH(+/+) cells. SIRT6 foci increase at both the global genome and at telomeric regions in H(2)O(2)-treated hMYH(+/+) cells. However, in untreated hMYH KO HEK-293T cells, SIRT6 foci only increase at the global genome, but not at the telomeric regions. In addition, the hMYH KO HEK-293T cells have increased extra-chromosomal and intra-chromosomal telomeres compared to the control cells, even in the absence of H(2)O(2) treatment. After H(2)O(2) treatment, the frequency of extra-chromosomal telomeres increased in control HEK-293T cells. Remarkably, in H(2)O(2)-treated hMYH KO cells, the frequencies of extra-chromosomal telomeres, intra-chromosomal telomeres, and telomere fusions are further increased. We further found that the sensitivity to H(2)O(2) and shortened telomeres of hMYH KO cells, are restored by expressing wild-type hMYH, and partially rescued by expressing hMYH(Q324H) mutant (defective in Hus1 interaction only), but not by expressing hMYH(V315A) mutant (defective in both SIRT6 and Hus1 interactions). Thus, MYH interactions with SIRT6 and Hus1 are critical for maintaining cell viability and telomeric stability. Therefore, the failure to coordinate 8-oxoG repair is detrimental to telomere integrity. 2022 2022-04-02 /pmc/articles/PMC9267527/ /pubmed/35812693 http://dx.doi.org/10.21926/obm.geriatr.2202196 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the conditions of the Creative Commons by Attribution License, which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is correctly cited. |
spellingShingle | Article Gupta, Aditi Hwang, Bor-Jang Benyamien-Roufaeil, Daniel Jain, Sara Liu, Sophie Gonzales, Rex Brown, Robert A. Zalzman, Michal Lu, A-Lien Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress |
title | Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress |
title_full | Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress |
title_fullStr | Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress |
title_full_unstemmed | Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress |
title_short | Mammalian MutY Homolog (MYH or MUTYH) is Critical for Telomere Integrity under Oxidative Stress |
title_sort | mammalian muty homolog (myh or mutyh) is critical for telomere integrity under oxidative stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267527/ https://www.ncbi.nlm.nih.gov/pubmed/35812693 http://dx.doi.org/10.21926/obm.geriatr.2202196 |
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