author_facet Lombard, D. B.
Schwer, B.
Alt, F. W.
Mostoslavsky, R.
Lombard, D. B.
Schwer, B.
Alt, F. W.
Mostoslavsky, R.
author Lombard, D. B.
Schwer, B.
Alt, F. W.
Mostoslavsky, R.
spellingShingle Lombard, D. B.
Schwer, B.
Alt, F. W.
Mostoslavsky, R.
Journal of Internal Medicine
SIRT6 in DNA repair, metabolism and ageing
Internal Medicine
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spelling Lombard, D. B. Schwer, B. Alt, F. W. Mostoslavsky, R. 0954-6820 1365-2796 Wiley Internal Medicine http://dx.doi.org/10.1111/j.1365-2796.2007.01902.x <jats:title>Abstract.</jats:title><jats:p>Ageing, or increased mortality with time, coupled with physiologic decline, is a nearly universal yet poorly understood biological phenomenon. Studies in model organisms suggest that two conserved pathways modulate longevity: DNA damage repair and Insulin/Igf1‐like signalling. In addition, homologs of yeast Sir2 – the sirtuins – regulate lifespan in diverse organisms. Here, we focus on one particular sirtuin, SIRT6. Mice lacking SIRT6 develop a degenerative disorder that in some respects mimics models of accelerated ageing [<jats:italic>Cell</jats:italic> (2006) <jats:bold>124</jats:bold>:315]. We discuss how sirtuins in general and SIRT6 specifically relate to other evolutionarily conserved pathways affecting ageing, and how SIRT6 might function to ensure organismal homeostasis and normal lifespan.</jats:p> SIRT6 in DNA repair, metabolism and ageing Journal of Internal Medicine
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title SIRT6 in DNA repair, metabolism and ageing
title_unstemmed SIRT6 in DNA repair, metabolism and ageing
title_full SIRT6 in DNA repair, metabolism and ageing
title_fullStr SIRT6 in DNA repair, metabolism and ageing
title_full_unstemmed SIRT6 in DNA repair, metabolism and ageing
title_short SIRT6 in DNA repair, metabolism and ageing
title_sort sirt6 in dna repair, metabolism and ageing
topic Internal Medicine
url http://dx.doi.org/10.1111/j.1365-2796.2007.01902.x
publishDate 2008
physical 128-141
description <jats:title>Abstract.</jats:title><jats:p>Ageing, or increased mortality with time, coupled with physiologic decline, is a nearly universal yet poorly understood biological phenomenon. Studies in model organisms suggest that two conserved pathways modulate longevity: DNA damage repair and Insulin/Igf1‐like signalling. In addition, homologs of yeast Sir2 – the sirtuins – regulate lifespan in diverse organisms. Here, we focus on one particular sirtuin, SIRT6. Mice lacking SIRT6 develop a degenerative disorder that in some respects mimics models of accelerated ageing [<jats:italic>Cell</jats:italic> (2006) <jats:bold>124</jats:bold>:315]. We discuss how sirtuins in general and SIRT6 specifically relate to other evolutionarily conserved pathways affecting ageing, and how SIRT6 might function to ensure organismal homeostasis and normal lifespan.</jats:p>
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author Lombard, D. B., Schwer, B., Alt, F. W., Mostoslavsky, R.
author_facet Lombard, D. B., Schwer, B., Alt, F. W., Mostoslavsky, R., Lombard, D. B., Schwer, B., Alt, F. W., Mostoslavsky, R.
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container_issue 2
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description <jats:title>Abstract.</jats:title><jats:p>Ageing, or increased mortality with time, coupled with physiologic decline, is a nearly universal yet poorly understood biological phenomenon. Studies in model organisms suggest that two conserved pathways modulate longevity: DNA damage repair and Insulin/Igf1‐like signalling. In addition, homologs of yeast Sir2 – the sirtuins – regulate lifespan in diverse organisms. Here, we focus on one particular sirtuin, SIRT6. Mice lacking SIRT6 develop a degenerative disorder that in some respects mimics models of accelerated ageing [<jats:italic>Cell</jats:italic> (2006) <jats:bold>124</jats:bold>:315]. We discuss how sirtuins in general and SIRT6 specifically relate to other evolutionarily conserved pathways affecting ageing, and how SIRT6 might function to ensure organismal homeostasis and normal lifespan.</jats:p>
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spelling Lombard, D. B. Schwer, B. Alt, F. W. Mostoslavsky, R. 0954-6820 1365-2796 Wiley Internal Medicine http://dx.doi.org/10.1111/j.1365-2796.2007.01902.x <jats:title>Abstract.</jats:title><jats:p>Ageing, or increased mortality with time, coupled with physiologic decline, is a nearly universal yet poorly understood biological phenomenon. Studies in model organisms suggest that two conserved pathways modulate longevity: DNA damage repair and Insulin/Igf1‐like signalling. In addition, homologs of yeast Sir2 – the sirtuins – regulate lifespan in diverse organisms. Here, we focus on one particular sirtuin, SIRT6. Mice lacking SIRT6 develop a degenerative disorder that in some respects mimics models of accelerated ageing [<jats:italic>Cell</jats:italic> (2006) <jats:bold>124</jats:bold>:315]. We discuss how sirtuins in general and SIRT6 specifically relate to other evolutionarily conserved pathways affecting ageing, and how SIRT6 might function to ensure organismal homeostasis and normal lifespan.</jats:p> SIRT6 in DNA repair, metabolism and ageing Journal of Internal Medicine
spellingShingle Lombard, D. B., Schwer, B., Alt, F. W., Mostoslavsky, R., Journal of Internal Medicine, SIRT6 in DNA repair, metabolism and ageing, Internal Medicine
title SIRT6 in DNA repair, metabolism and ageing
title_full SIRT6 in DNA repair, metabolism and ageing
title_fullStr SIRT6 in DNA repair, metabolism and ageing
title_full_unstemmed SIRT6 in DNA repair, metabolism and ageing
title_short SIRT6 in DNA repair, metabolism and ageing
title_sort sirt6 in dna repair, metabolism and ageing
title_unstemmed SIRT6 in DNA repair, metabolism and ageing
topic Internal Medicine
url http://dx.doi.org/10.1111/j.1365-2796.2007.01902.x