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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Research Network of Computational and Structural Biotechnology (RNCSB) Organization
2013
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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. |
format | Online Article Text |
id | pubmed-3962127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Research Network of Computational and Structural Biotechnology (RNCSB) Organization |
record_format | MEDLINE/PubMed |
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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