A DOG’s View of Fanconi Anemia: Insights from C. elegans

C. elegans provides an excellent model system for the study of the Fanconi Anemia (FA), one of the hallmarks of which is sensitivity to interstrand crosslinking agents. Central to our understanding of FA has been the investigation of DOG-1, the functional ortholog of the deadbox helicase FANCJ. Here...

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Main Authors: Martin Jones, Ann Rose
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Anemia
Online Access:http://dx.doi.org/10.1155/2012/323721
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spelling doaj-24bd71c972fd4c629407a250e4f6c9982020-11-24T21:40:04ZengHindawi LimitedAnemia2090-12672090-12752012-01-01201210.1155/2012/323721323721A DOG’s View of Fanconi Anemia: Insights from C. elegansMartin Jones0Ann Rose1Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaDepartment of Medical Genetics, University of British Columbia, Vancouver, BC, V6T 1Z4, CanadaC. elegans provides an excellent model system for the study of the Fanconi Anemia (FA), one of the hallmarks of which is sensitivity to interstrand crosslinking agents. Central to our understanding of FA has been the investigation of DOG-1, the functional ortholog of the deadbox helicase FANCJ. Here we review the current understanding of the unique role of DOG-1 in maintaining stability of G-rich DNA in C. elegans and explore the question of why DOG-1 animals are crosslink sensitive. We propose a dynamic model in which noncovalently linked G-rich structures form and un-form in the presence of DOG-1. When DOG-1 is absent but crosslinking agents are present the G-rich structures are readily covalently crosslinked, resulting in increased crosslinks formation and thus giving increased crosslink sensitivity. In this interpretation DOG-1 is neither upstream nor downstream in the FA pathway, but works alongside it to limit the availability of crosslink substrates. This model reconciles the crosslink sensitivity observed in the absence of DOG-1 function with its unique role in maintaining G-Rich DNA and will help to formulate experiments to test this hypothesis.http://dx.doi.org/10.1155/2012/323721
collection DOAJ
language English
format Article
sources DOAJ
author Martin Jones
Ann Rose
spellingShingle Martin Jones
Ann Rose
A DOG’s View of Fanconi Anemia: Insights from C. elegans
Anemia
author_facet Martin Jones
Ann Rose
author_sort Martin Jones
title A DOG’s View of Fanconi Anemia: Insights from C. elegans
title_short A DOG’s View of Fanconi Anemia: Insights from C. elegans
title_full A DOG’s View of Fanconi Anemia: Insights from C. elegans
title_fullStr A DOG’s View of Fanconi Anemia: Insights from C. elegans
title_full_unstemmed A DOG’s View of Fanconi Anemia: Insights from C. elegans
title_sort dog’s view of fanconi anemia: insights from c. elegans
publisher Hindawi Limited
series Anemia
issn 2090-1267
2090-1275
publishDate 2012-01-01
description C. elegans provides an excellent model system for the study of the Fanconi Anemia (FA), one of the hallmarks of which is sensitivity to interstrand crosslinking agents. Central to our understanding of FA has been the investigation of DOG-1, the functional ortholog of the deadbox helicase FANCJ. Here we review the current understanding of the unique role of DOG-1 in maintaining stability of G-rich DNA in C. elegans and explore the question of why DOG-1 animals are crosslink sensitive. We propose a dynamic model in which noncovalently linked G-rich structures form and un-form in the presence of DOG-1. When DOG-1 is absent but crosslinking agents are present the G-rich structures are readily covalently crosslinked, resulting in increased crosslinks formation and thus giving increased crosslink sensitivity. In this interpretation DOG-1 is neither upstream nor downstream in the FA pathway, but works alongside it to limit the availability of crosslink substrates. This model reconciles the crosslink sensitivity observed in the absence of DOG-1 function with its unique role in maintaining G-Rich DNA and will help to formulate experiments to test this hypothesis.
url http://dx.doi.org/10.1155/2012/323721
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