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Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages

In budding yeast, the Sir2, Sir3 and Sir4 proteins form SIR complexes, required for the assembly of silent heterochromatin domains, and which mediate transcription silencing at the telomeres as well as at silent mating type loci. In this study, under fluorescence microscopy, we found most Sir3-GFP e...

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Autores principales: Tung, Shu-Yun, Lee, Kuan-Wei, Hong, Jia-Yang, Lee, Sue-Ping, Shen, Hsiao-Hsuian, Liou, Gunn-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology (RNCSB) Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962127/
https://www.ncbi.nlm.nih.gov/pubmed/24688731
http://dx.doi.org/10.5936/csbj.201304001
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author Tung, Shu-Yun
Lee, Kuan-Wei
Hong, Jia-Yang
Lee, Sue-Ping
Shen, Hsiao-Hsuian
Liou, Gunn-Guang
author_facet Tung, Shu-Yun
Lee, Kuan-Wei
Hong, Jia-Yang
Lee, Sue-Ping
Shen, Hsiao-Hsuian
Liou, Gunn-Guang
author_sort Tung, Shu-Yun
collection PubMed
description In budding yeast, the Sir2, Sir3 and Sir4 proteins form SIR complexes, required for the assembly of silent heterochromatin domains, and which mediate transcription silencing at the telomeres as well as at silent mating type loci. In this study, under fluorescence microscopy, we found most Sir3-GFP expressions in the logarithmic phase cells appeared as multiple punctations as expected. However, some differences in the distribution of fluorescent signals were detected in the diauxic~early stationary phase cells. To clarify these, we then used ChIP on chip assays to investigate the genome-wide localization of Sir3. In general, Sir3 binds to all 32 telomere proximal regions, the silent mating type loci and also binds to the rDNA region. However, the genome-wide localization patterns of Sir3 are different between these two distinct growth phases. We also confirmed that Sir3 binds to a recently identified secondary binding site, PAU genes, and further identified 349 Sir3-associated cluster regions. These results provide additional support in roles for Sir3 in the modulation of gene expression during physical conditions such as diauxic~early stationary phase growing. Moreover, they imply that Sir3 may be not only involved in the formation of conventional silent heterochromatin, but also able to associate with some other chromatin regions involved in epigenetic regulation.
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spelling pubmed-39621272014-03-31 Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages Tung, Shu-Yun Lee, Kuan-Wei Hong, Jia-Yang Lee, Sue-Ping Shen, Hsiao-Hsuian Liou, Gunn-Guang Comput Struct Biotechnol J Research Articles In budding yeast, the Sir2, Sir3 and Sir4 proteins form SIR complexes, required for the assembly of silent heterochromatin domains, and which mediate transcription silencing at the telomeres as well as at silent mating type loci. In this study, under fluorescence microscopy, we found most Sir3-GFP expressions in the logarithmic phase cells appeared as multiple punctations as expected. However, some differences in the distribution of fluorescent signals were detected in the diauxic~early stationary phase cells. To clarify these, we then used ChIP on chip assays to investigate the genome-wide localization of Sir3. In general, Sir3 binds to all 32 telomere proximal regions, the silent mating type loci and also binds to the rDNA region. However, the genome-wide localization patterns of Sir3 are different between these two distinct growth phases. We also confirmed that Sir3 binds to a recently identified secondary binding site, PAU genes, and further identified 349 Sir3-associated cluster regions. These results provide additional support in roles for Sir3 in the modulation of gene expression during physical conditions such as diauxic~early stationary phase growing. Moreover, they imply that Sir3 may be not only involved in the formation of conventional silent heterochromatin, but also able to associate with some other chromatin regions involved in epigenetic regulation. Research Network of Computational and Structural Biotechnology (RNCSB) Organization 2013-06-19 /pmc/articles/PMC3962127/ /pubmed/24688731 http://dx.doi.org/10.5936/csbj.201304001 Text en © Tung et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly cited.
spellingShingle Research Articles
Tung, Shu-Yun
Lee, Kuan-Wei
Hong, Jia-Yang
Lee, Sue-Ping
Shen, Hsiao-Hsuian
Liou, Gunn-Guang
Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages
title Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages
title_full Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages
title_fullStr Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages
title_full_unstemmed Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages
title_short Changes in the genome-wide localization pattern of Sir3 in Saccharomyces cerevisiae during different growth stages
title_sort changes in the genome-wide localization pattern of sir3 in saccharomyces cerevisiae during different growth stages
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962127/
https://www.ncbi.nlm.nih.gov/pubmed/24688731
http://dx.doi.org/10.5936/csbj.201304001
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