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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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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. |
format | Online Article Text |
id | pubmed-3591859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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