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Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana

BACKGROUND: Telomeres are indispensable for genome stability maintenance. They are maintained by the telomere-associated protein complex, which include Ku proteins and a telomerase among others. Here, we investigated a role of Ku80 in Leishmania mexicana. Leishmania is a genus of parasitic protists...

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Autores principales: Poláková, Ester, Albanaz, Amanda T. S., Zakharova, Alexandra, Novozhilova, Tatiana S., Gerasimov, Evgeny S., Yurchenko, Vyacheslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716037/
https://www.ncbi.nlm.nih.gov/pubmed/34965251
http://dx.doi.org/10.1371/journal.pntd.0010041
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author Poláková, Ester
Albanaz, Amanda T. S.
Zakharova, Alexandra
Novozhilova, Tatiana S.
Gerasimov, Evgeny S.
Yurchenko, Vyacheslav
author_facet Poláková, Ester
Albanaz, Amanda T. S.
Zakharova, Alexandra
Novozhilova, Tatiana S.
Gerasimov, Evgeny S.
Yurchenko, Vyacheslav
author_sort Poláková, Ester
collection PubMed
description BACKGROUND: Telomeres are indispensable for genome stability maintenance. They are maintained by the telomere-associated protein complex, which include Ku proteins and a telomerase among others. Here, we investigated a role of Ku80 in Leishmania mexicana. Leishmania is a genus of parasitic protists of the family Trypanosomatidae causing a vector-born disease called leishmaniasis. METHODOLOGY/PRINCIPAL FINDINGS: We used the previously established CRISPR/Cas9 system to mediate ablation of Ku80- and Ku70-encoding genes in L. mexicana. Complete knock-outs of both genes were confirmed by Southern blotting, whole-genome Illumina sequencing, and RT-qPCR. Resulting telomeric phenotypes were subsequently investigated using Southern blotting detection of terminal restriction fragments. The genome integrity in the Ku80- deficient cells was further investigated by whole-genome sequencing. Our work revealed that telomeres in the ΔKu80 L. mexicana are elongated compared to those of the wild type. This is a surprising finding considering that in another model trypanosomatid, Trypanosoma brucei, they are shortened upon ablation of the same gene. A telomere elongation phenotype has been documented in other species and associated with a presence of telomerase-independent alternative telomere lengthening pathway. Our results also showed that Ku80 appears to be not involved in genome stability maintenance in L. mexicana. CONCLUSION/SIGNIFICANCE: Ablation of the Ku proteins in L. mexicana triggers telomere elongation, but does not have an adverse impact on genome integrity.
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spelling pubmed-87160372021-12-30 Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana Poláková, Ester Albanaz, Amanda T. S. Zakharova, Alexandra Novozhilova, Tatiana S. Gerasimov, Evgeny S. Yurchenko, Vyacheslav PLoS Negl Trop Dis Research Article BACKGROUND: Telomeres are indispensable for genome stability maintenance. They are maintained by the telomere-associated protein complex, which include Ku proteins and a telomerase among others. Here, we investigated a role of Ku80 in Leishmania mexicana. Leishmania is a genus of parasitic protists of the family Trypanosomatidae causing a vector-born disease called leishmaniasis. METHODOLOGY/PRINCIPAL FINDINGS: We used the previously established CRISPR/Cas9 system to mediate ablation of Ku80- and Ku70-encoding genes in L. mexicana. Complete knock-outs of both genes were confirmed by Southern blotting, whole-genome Illumina sequencing, and RT-qPCR. Resulting telomeric phenotypes were subsequently investigated using Southern blotting detection of terminal restriction fragments. The genome integrity in the Ku80- deficient cells was further investigated by whole-genome sequencing. Our work revealed that telomeres in the ΔKu80 L. mexicana are elongated compared to those of the wild type. This is a surprising finding considering that in another model trypanosomatid, Trypanosoma brucei, they are shortened upon ablation of the same gene. A telomere elongation phenotype has been documented in other species and associated with a presence of telomerase-independent alternative telomere lengthening pathway. Our results also showed that Ku80 appears to be not involved in genome stability maintenance in L. mexicana. CONCLUSION/SIGNIFICANCE: Ablation of the Ku proteins in L. mexicana triggers telomere elongation, but does not have an adverse impact on genome integrity. Public Library of Science 2021-12-29 /pmc/articles/PMC8716037/ /pubmed/34965251 http://dx.doi.org/10.1371/journal.pntd.0010041 Text en © 2021 Poláková et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Poláková, Ester
Albanaz, Amanda T. S.
Zakharova, Alexandra
Novozhilova, Tatiana S.
Gerasimov, Evgeny S.
Yurchenko, Vyacheslav
Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana
title Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana
title_full Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana
title_fullStr Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana
title_full_unstemmed Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana
title_short Ku80 is involved in telomere maintenance but dispensable for genomic stability in Leishmania mexicana
title_sort ku80 is involved in telomere maintenance but dispensable for genomic stability in leishmania mexicana
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716037/
https://www.ncbi.nlm.nih.gov/pubmed/34965251
http://dx.doi.org/10.1371/journal.pntd.0010041
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