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Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

Dyskeratosis congenita (DC) and its phenotypically severe variant, Hoyeraal-Hreidarsson syndrome (HHS), are multisystem bone-marrow-failure syndromes in which the principal pathology is defective telomere maintenance. The genetic basis of many cases of DC and HHS remains unknown. Using whole-exome s...

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Autores principales: Walne, Amanda J., Vulliamy, Tom, Kirwan, Michael, Plagnol, Vincent, Dokal, Inderjeet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591859/
https://www.ncbi.nlm.nih.gov/pubmed/23453664
http://dx.doi.org/10.1016/j.ajhg.2013.02.001
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author Walne, Amanda J.
Vulliamy, Tom
Kirwan, Michael
Plagnol, Vincent
Dokal, Inderjeet
author_facet Walne, Amanda J.
Vulliamy, Tom
Kirwan, Michael
Plagnol, Vincent
Dokal, Inderjeet
author_sort Walne, Amanda J.
collection PubMed
description Dyskeratosis congenita (DC) and its phenotypically severe variant, Hoyeraal-Hreidarsson syndrome (HHS), are multisystem bone-marrow-failure syndromes in which the principal pathology is defective telomere maintenance. The genetic basis of many cases of DC and HHS remains unknown. Using whole-exome sequencing, we identified biallelic mutations in RTEL1, encoding a helicase essential for telomere maintenance and regulation of homologous recombination, in an individual with familial HHS. Additional screening of RTEL1 identified biallelic mutations in 6/23 index cases with HHS but none in 102 DC or DC-like cases. All 11 mutations in ten HHS individuals from seven families segregated in an autosomal-recessive manner, and telomere lengths were significantly shorter in cases than in controls (p = 0.0003). This group had significantly higher levels of telomeric circles, produced as a consequence of incorrect processing of telomere ends, than did controls (p = 0.0148). These biallelic RTEL1 mutations are responsible for a major subgroup (∼29%) of HHS. Our studies show that cells harboring these mutations have significant defects in telomere maintenance, but not in homologous recombination, and that incorrect resolution of T-loops is a mechanism for telomere shortening and disease causation in humans. They also demonstrate the severe multisystem consequences of its dysfunction.
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spelling pubmed-35918592013-09-07 Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita Walne, Amanda J. Vulliamy, Tom Kirwan, Michael Plagnol, Vincent Dokal, Inderjeet Am J Hum Genet Report Dyskeratosis congenita (DC) and its phenotypically severe variant, Hoyeraal-Hreidarsson syndrome (HHS), are multisystem bone-marrow-failure syndromes in which the principal pathology is defective telomere maintenance. The genetic basis of many cases of DC and HHS remains unknown. Using whole-exome sequencing, we identified biallelic mutations in RTEL1, encoding a helicase essential for telomere maintenance and regulation of homologous recombination, in an individual with familial HHS. Additional screening of RTEL1 identified biallelic mutations in 6/23 index cases with HHS but none in 102 DC or DC-like cases. All 11 mutations in ten HHS individuals from seven families segregated in an autosomal-recessive manner, and telomere lengths were significantly shorter in cases than in controls (p = 0.0003). This group had significantly higher levels of telomeric circles, produced as a consequence of incorrect processing of telomere ends, than did controls (p = 0.0148). These biallelic RTEL1 mutations are responsible for a major subgroup (∼29%) of HHS. Our studies show that cells harboring these mutations have significant defects in telomere maintenance, but not in homologous recombination, and that incorrect resolution of T-loops is a mechanism for telomere shortening and disease causation in humans. They also demonstrate the severe multisystem consequences of its dysfunction. Elsevier 2013-03-07 /pmc/articles/PMC3591859/ /pubmed/23453664 http://dx.doi.org/10.1016/j.ajhg.2013.02.001 Text en © 2013 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Report
Walne, Amanda J.
Vulliamy, Tom
Kirwan, Michael
Plagnol, Vincent
Dokal, Inderjeet
Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
title Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
title_full Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
title_fullStr Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
title_full_unstemmed Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
title_short Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
title_sort constitutional mutations in rtel1 cause severe dyskeratosis congenita
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591859/
https://www.ncbi.nlm.nih.gov/pubmed/23453664
http://dx.doi.org/10.1016/j.ajhg.2013.02.001
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