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Smc5/6 in the rDNA modulates lifespan independently of Fob1​

The ribosomal DNA (rDNA) in Saccharomyces cerevisiae is in one tandem repeat array on Chromosome XII. Two regions within each repetitive element, called intergenic spacer 1 (IGS1) and IGS2, are important for organizing the rDNA within the nucleolus. The Smc5/6 complex localizes to IGS1 and IGS2. We...

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Autores principales: Moradi‐Fard, Sarah, Mojumdar, Aditya, Chan, Megan, Harkness, Troy A.A., Cobb, Jennifer A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208791/
https://www.ncbi.nlm.nih.gov/pubmed/33979898
http://dx.doi.org/10.1111/acel.13373
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author Moradi‐Fard, Sarah
Mojumdar, Aditya
Chan, Megan
Harkness, Troy A.A.
Cobb, Jennifer A.
author_facet Moradi‐Fard, Sarah
Mojumdar, Aditya
Chan, Megan
Harkness, Troy A.A.
Cobb, Jennifer A.
author_sort Moradi‐Fard, Sarah
collection PubMed
description The ribosomal DNA (rDNA) in Saccharomyces cerevisiae is in one tandem repeat array on Chromosome XII. Two regions within each repetitive element, called intergenic spacer 1 (IGS1) and IGS2, are important for organizing the rDNA within the nucleolus. The Smc5/6 complex localizes to IGS1 and IGS2. We show that Smc5/6 has a function in the rDNA beyond its role in homologous recombination (HR) at the replication fork barrier (RFB) located in IGS1. Fob1 is required for optimal binding of Smc5/6 at IGS1 whereas the canonical silencing factor Sir2 is required for its optimal binding at IGS2, independently of Fob1. Through interdependent interactions, Smc5/6 stabilizes Sir2 and Cohibin at both IGS and its recovery at IGS2 is important for nucleolar compaction and transcriptional silencing, which in turn supports rDNA stability and lifespan.
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spelling pubmed-82087912021-06-25 Smc5/6 in the rDNA modulates lifespan independently of Fob1​ Moradi‐Fard, Sarah Mojumdar, Aditya Chan, Megan Harkness, Troy A.A. Cobb, Jennifer A. Aging Cell Original Articles The ribosomal DNA (rDNA) in Saccharomyces cerevisiae is in one tandem repeat array on Chromosome XII. Two regions within each repetitive element, called intergenic spacer 1 (IGS1) and IGS2, are important for organizing the rDNA within the nucleolus. The Smc5/6 complex localizes to IGS1 and IGS2. We show that Smc5/6 has a function in the rDNA beyond its role in homologous recombination (HR) at the replication fork barrier (RFB) located in IGS1. Fob1 is required for optimal binding of Smc5/6 at IGS1 whereas the canonical silencing factor Sir2 is required for its optimal binding at IGS2, independently of Fob1. Through interdependent interactions, Smc5/6 stabilizes Sir2 and Cohibin at both IGS and its recovery at IGS2 is important for nucleolar compaction and transcriptional silencing, which in turn supports rDNA stability and lifespan. John Wiley and Sons Inc. 2021-05-12 2021-06 /pmc/articles/PMC8208791/ /pubmed/33979898 http://dx.doi.org/10.1111/acel.13373 Text en © 2021 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Moradi‐Fard, Sarah
Mojumdar, Aditya
Chan, Megan
Harkness, Troy A.A.
Cobb, Jennifer A.
Smc5/6 in the rDNA modulates lifespan independently of Fob1​
title Smc5/6 in the rDNA modulates lifespan independently of Fob1​
title_full Smc5/6 in the rDNA modulates lifespan independently of Fob1​
title_fullStr Smc5/6 in the rDNA modulates lifespan independently of Fob1​
title_full_unstemmed Smc5/6 in the rDNA modulates lifespan independently of Fob1​
title_short Smc5/6 in the rDNA modulates lifespan independently of Fob1​
title_sort smc5/6 in the rdna modulates lifespan independently of fob1​
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208791/
https://www.ncbi.nlm.nih.gov/pubmed/33979898
http://dx.doi.org/10.1111/acel.13373
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