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The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region
In Neurospora crassa, the methionine synthase gene met-8 plays a key role in methionine synthesis. In this study, we found that MET-8 protein levels were compromised in several mutants defective in proper heterochromatin formation. Bioinformatics analysis revealed a 50-kb AT-rich region adjacent to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041435/ https://www.ncbi.nlm.nih.gov/pubmed/24711369 http://dx.doi.org/10.1093/nar/gku261 |
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author | Yang, Silu Li, Weihua Qi, Shaohua Gai, Kexin Chen, Yibo Suo, Jingxia Cao, Yingqiong He, Yubo Wang, Ying He, Qun |
author_facet | Yang, Silu Li, Weihua Qi, Shaohua Gai, Kexin Chen, Yibo Suo, Jingxia Cao, Yingqiong He, Yubo Wang, Ying He, Qun |
author_sort | Yang, Silu |
collection | PubMed |
description | In Neurospora crassa, the methionine synthase gene met-8 plays a key role in methionine synthesis. In this study, we found that MET-8 protein levels were compromised in several mutants defective in proper heterochromatin formation. Bioinformatics analysis revealed a 50-kb AT-rich region adjacent to the met-8 promoter. ChIP assays confirmed that trimethylated H3K9 was enriched in this region, indicating that heterochromatin may form upstream of met-8. In an H3K9R mutant strain, the output of met-8 was dramatically reduced, similar to what we observed in mutant strains that had defective heterochromatin formation. Furthermore, the production of ectopically expressed met-8 at the his-3 locus in the absence of a normal heterochromatin environment was inefficient, whereas ectopic expression of met-8 downstream of two other heterochromatin domains was efficient. In addition, our data show that the expression of mig-6 was also controlled by an upstream 4.2-kb AT-rich region similar to that of the met-8 gene, and we demonstrate that the AT-rich regions adjacent to met-8 or mig-6 are required for their peak expression. Our study indicates that met-8 and mig-6 may represent a novel type of gene, whose expression relies on the proper formation of a nearby heterochromatin region. |
format | Online Article Text |
id | pubmed-4041435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40414352014-06-11 The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region Yang, Silu Li, Weihua Qi, Shaohua Gai, Kexin Chen, Yibo Suo, Jingxia Cao, Yingqiong He, Yubo Wang, Ying He, Qun Nucleic Acids Res Gene regulation, Chromatin and Epigenetics In Neurospora crassa, the methionine synthase gene met-8 plays a key role in methionine synthesis. In this study, we found that MET-8 protein levels were compromised in several mutants defective in proper heterochromatin formation. Bioinformatics analysis revealed a 50-kb AT-rich region adjacent to the met-8 promoter. ChIP assays confirmed that trimethylated H3K9 was enriched in this region, indicating that heterochromatin may form upstream of met-8. In an H3K9R mutant strain, the output of met-8 was dramatically reduced, similar to what we observed in mutant strains that had defective heterochromatin formation. Furthermore, the production of ectopically expressed met-8 at the his-3 locus in the absence of a normal heterochromatin environment was inefficient, whereas ectopic expression of met-8 downstream of two other heterochromatin domains was efficient. In addition, our data show that the expression of mig-6 was also controlled by an upstream 4.2-kb AT-rich region similar to that of the met-8 gene, and we demonstrate that the AT-rich regions adjacent to met-8 or mig-6 are required for their peak expression. Our study indicates that met-8 and mig-6 may represent a novel type of gene, whose expression relies on the proper formation of a nearby heterochromatin region. Oxford University Press 2014-06-01 2014-04-07 /pmc/articles/PMC4041435/ /pubmed/24711369 http://dx.doi.org/10.1093/nar/gku261 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Yang, Silu Li, Weihua Qi, Shaohua Gai, Kexin Chen, Yibo Suo, Jingxia Cao, Yingqiong He, Yubo Wang, Ying He, Qun The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region |
title | The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region |
title_full | The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region |
title_fullStr | The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region |
title_full_unstemmed | The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region |
title_short | The highly expressed methionine synthase gene of Neurospora crassa is positively regulated by its proximal heterochromatic region |
title_sort | highly expressed methionine synthase gene of neurospora crassa is positively regulated by its proximal heterochromatic region |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041435/ https://www.ncbi.nlm.nih.gov/pubmed/24711369 http://dx.doi.org/10.1093/nar/gku261 |
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