The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination.
The heterodimeric Ku complex has been shown to participate in DNA repair and telomere regulation in a variety of organisms. Here we report a detailed characterization of the function of Ku70 in the diploid fungal pathogen Candida albicans. Both ku70 heterozygous and homozygous deletion mutants have...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2011-01-01
|
Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21886818/?tool=EBI |
_version_ | 1818402863492104192 |
---|---|
author | Lidia Chico Toni Ciudad Min Hsu Neal F Lue Germán Larriba |
author_facet | Lidia Chico Toni Ciudad Min Hsu Neal F Lue Germán Larriba |
author_sort | Lidia Chico |
collection | DOAJ |
description | The heterodimeric Ku complex has been shown to participate in DNA repair and telomere regulation in a variety of organisms. Here we report a detailed characterization of the function of Ku70 in the diploid fungal pathogen Candida albicans. Both ku70 heterozygous and homozygous deletion mutants have a wild-type colony and cellular morphology, and are not sensitive to MMS or UV light. Interestingly, we observed complex effects of KU70 gene dosage on telomere lengths, with the KU70/ku70 heterozygotes exhibiting slightly shorter telomeres, and the ku70 null strain exhibiting long and heterogeneous telomeres. Analysis of combination mutants suggests that the telomere elongation in the ku70 null mutant is due mostly to unregulated telomerase action. In addition, elevated levels of extrachromosomal telomeric circles were detected in the null mutant, consistent with activation of aberrant telomeric recombination. Altogether, our observations point to multiple mechanisms of the Ku complex in telomerase regulation and telomere protection in C. albicans, and reveal interesting similarities and differences in the mechanisms of the Ku complex in disparate systems. |
first_indexed | 2024-12-14T08:15:07Z |
format | Article |
id | doaj.art-a6a023e3682d4b13a61607351dc3c509 |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-14T08:15:07Z |
publishDate | 2011-01-01 |
publisher | Public Library of Science (PLoS) |
record_format | Article |
series | PLoS ONE |
spelling | doaj.art-a6a023e3682d4b13a61607351dc3c5092022-12-21T23:09:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0168e2373210.1371/journal.pone.0023732The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination.Lidia ChicoToni CiudadMin HsuNeal F LueGermán LarribaThe heterodimeric Ku complex has been shown to participate in DNA repair and telomere regulation in a variety of organisms. Here we report a detailed characterization of the function of Ku70 in the diploid fungal pathogen Candida albicans. Both ku70 heterozygous and homozygous deletion mutants have a wild-type colony and cellular morphology, and are not sensitive to MMS or UV light. Interestingly, we observed complex effects of KU70 gene dosage on telomere lengths, with the KU70/ku70 heterozygotes exhibiting slightly shorter telomeres, and the ku70 null strain exhibiting long and heterogeneous telomeres. Analysis of combination mutants suggests that the telomere elongation in the ku70 null mutant is due mostly to unregulated telomerase action. In addition, elevated levels of extrachromosomal telomeric circles were detected in the null mutant, consistent with activation of aberrant telomeric recombination. Altogether, our observations point to multiple mechanisms of the Ku complex in telomerase regulation and telomere protection in C. albicans, and reveal interesting similarities and differences in the mechanisms of the Ku complex in disparate systems.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21886818/?tool=EBI |
spellingShingle | Lidia Chico Toni Ciudad Min Hsu Neal F Lue Germán Larriba The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination. PLoS ONE |
title | The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination. |
title_full | The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination. |
title_fullStr | The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination. |
title_full_unstemmed | The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination. |
title_short | The Candida albicans Ku70 modulates telomere length and structure by regulating both telomerase and recombination. |
title_sort | candida albicans ku70 modulates telomere length and structure by regulating both telomerase and recombination |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21886818/?tool=EBI |
work_keys_str_mv | AT lidiachico thecandidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT toniciudad thecandidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT minhsu thecandidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT nealflue thecandidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT germanlarriba thecandidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT lidiachico candidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT toniciudad candidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT minhsu candidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT nealflue candidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination AT germanlarriba candidaalbicansku70modulatestelomerelengthandstructurebyregulatingbothtelomeraseandrecombination |