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Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV

In the absence of the telomerase, telomeres undergo progressive shortening and are ultimately recruited into end-to-end chromosome fusions via the non-homologous end joining (NHEJ) double-strand break repair pathway. Previously, we showed that fusion of critically shortened telomeres in Arabidopsis...

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Autores principales: Heacock, Michelle L., Idol, Rachel A., Friesner, Joanna D., Britt, Anne B., Shippen, Dorothy E.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2095805/
https://www.ncbi.nlm.nih.gov/pubmed/17897968
http://dx.doi.org/10.1093/nar/gkm472
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author Heacock, Michelle L.
Idol, Rachel A.
Friesner, Joanna D.
Britt, Anne B.
Shippen, Dorothy E.
author_facet Heacock, Michelle L.
Idol, Rachel A.
Friesner, Joanna D.
Britt, Anne B.
Shippen, Dorothy E.
author_sort Heacock, Michelle L.
collection PubMed
description In the absence of the telomerase, telomeres undergo progressive shortening and are ultimately recruited into end-to-end chromosome fusions via the non-homologous end joining (NHEJ) double-strand break repair pathway. Previously, we showed that fusion of critically shortened telomeres in Arabidopsis proceeds with approximately the same efficiency in the presence or absence of KU70, a key component of NHEJ. Here we report that DNA ligase IV (LIG4) is also not essential for telomere joining. We observed only a modest decrease (3-fold) in the frequency of chromosome fusions in triple tert ku70 lig4 mutants versus tert ku70 or tert. Sequence analysis revealed that, relative to tert ku70, chromosome fusion junctions in tert ku70 lig4 mutants contained less microhomology and less telomeric DNA. These findings argue that the KU-LIG4 independent end-joining pathway is less efficient and mechanistically distinct from KU-independent NHEJ. Strikingly, in all the genetic backgrounds we tested, chromosome fusions are initiated when the shortest telomere in the population reaches ∼1 kb, implying that this size represents a critical threshold that heralds a detrimental structural transition. These data reveal the transitory nature of telomere stability, and the robust and flexible nature of DNA repair mechanisms elicited by telomere dysfunction.
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spelling pubmed-20958052007-12-07 Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV Heacock, Michelle L. Idol, Rachel A. Friesner, Joanna D. Britt, Anne B. Shippen, Dorothy E. Nucleic Acids Res Molecular Biology In the absence of the telomerase, telomeres undergo progressive shortening and are ultimately recruited into end-to-end chromosome fusions via the non-homologous end joining (NHEJ) double-strand break repair pathway. Previously, we showed that fusion of critically shortened telomeres in Arabidopsis proceeds with approximately the same efficiency in the presence or absence of KU70, a key component of NHEJ. Here we report that DNA ligase IV (LIG4) is also not essential for telomere joining. We observed only a modest decrease (3-fold) in the frequency of chromosome fusions in triple tert ku70 lig4 mutants versus tert ku70 or tert. Sequence analysis revealed that, relative to tert ku70, chromosome fusion junctions in tert ku70 lig4 mutants contained less microhomology and less telomeric DNA. These findings argue that the KU-LIG4 independent end-joining pathway is less efficient and mechanistically distinct from KU-independent NHEJ. Strikingly, in all the genetic backgrounds we tested, chromosome fusions are initiated when the shortest telomere in the population reaches ∼1 kb, implying that this size represents a critical threshold that heralds a detrimental structural transition. These data reveal the transitory nature of telomere stability, and the robust and flexible nature of DNA repair mechanisms elicited by telomere dysfunction. Oxford University Press 2007-10 2007-09-25 /pmc/articles/PMC2095805/ /pubmed/17897968 http://dx.doi.org/10.1093/nar/gkm472 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Heacock, Michelle L.
Idol, Rachel A.
Friesner, Joanna D.
Britt, Anne B.
Shippen, Dorothy E.
Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV
title Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV
title_full Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV
title_fullStr Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV
title_full_unstemmed Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV
title_short Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV
title_sort telomere dynamics and fusion of critically shortened telomeres in plants lacking dna ligase iv
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2095805/
https://www.ncbi.nlm.nih.gov/pubmed/17897968
http://dx.doi.org/10.1093/nar/gkm472
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