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Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans
Gene-silencing mechanisms are being shown to be associated with an increasing number of fungal developmental processes. Telomere position effect (TPE) is a eukaryotic phenomenon resulting in gene repression in areas immediately adjacent to telomere caps. Here, TPE is shown to regulate expression of...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068700/ https://www.ncbi.nlm.nih.gov/pubmed/20724388 http://dx.doi.org/10.1099/mic.0.039255-0 |
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author | Palmer, Jonathan M. Mallaredy, Sandeep Perry, Dustin W. Sanchez, James F. Theisen, Jeffrey M. Szewczyk, Edyta Oakley, Berl R. Wang, Clay C. C. Keller, Nancy P. Mirabito, Peter M. |
author_facet | Palmer, Jonathan M. Mallaredy, Sandeep Perry, Dustin W. Sanchez, James F. Theisen, Jeffrey M. Szewczyk, Edyta Oakley, Berl R. Wang, Clay C. C. Keller, Nancy P. Mirabito, Peter M. |
author_sort | Palmer, Jonathan M. |
collection | PubMed |
description | Gene-silencing mechanisms are being shown to be associated with an increasing number of fungal developmental processes. Telomere position effect (TPE) is a eukaryotic phenomenon resulting in gene repression in areas immediately adjacent to telomere caps. Here, TPE is shown to regulate expression of transgenes on the left arm of chromosome III and the right arm of chromosome VI in Aspergillus nidulans. Phenotypes found to be associated with transgene repression included reduction in radial growth and the absence of sexual spores; however, these pleiotropic phenotypes were remedied when cultures were grown on media with appropriate supplementation. Simple radial growth and ascosporogenesis assays provided insights into the mechanism of TPE, including a means to determine its extent. These experiments revealed that the KU70 homologue (NkuA) and the heterochromatin-associated proteins HepA, ClrD and HdaA were partially required for transgene silencing. This study indicates that TPE extends at least 30 kb on chromosome III, suggesting that this phenomenon may be important for gene regulation in subtelomeric regions of A. nidulans. |
format | Text |
id | pubmed-3068700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-30687002011-12-01 Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans Palmer, Jonathan M. Mallaredy, Sandeep Perry, Dustin W. Sanchez, James F. Theisen, Jeffrey M. Szewczyk, Edyta Oakley, Berl R. Wang, Clay C. C. Keller, Nancy P. Mirabito, Peter M. Microbiology (Reading) Cell and Molecular Biology of Microbes Gene-silencing mechanisms are being shown to be associated with an increasing number of fungal developmental processes. Telomere position effect (TPE) is a eukaryotic phenomenon resulting in gene repression in areas immediately adjacent to telomere caps. Here, TPE is shown to regulate expression of transgenes on the left arm of chromosome III and the right arm of chromosome VI in Aspergillus nidulans. Phenotypes found to be associated with transgene repression included reduction in radial growth and the absence of sexual spores; however, these pleiotropic phenotypes were remedied when cultures were grown on media with appropriate supplementation. Simple radial growth and ascosporogenesis assays provided insights into the mechanism of TPE, including a means to determine its extent. These experiments revealed that the KU70 homologue (NkuA) and the heterochromatin-associated proteins HepA, ClrD and HdaA were partially required for transgene silencing. This study indicates that TPE extends at least 30 kb on chromosome III, suggesting that this phenomenon may be important for gene regulation in subtelomeric regions of A. nidulans. Microbiology Society 2010-12 /pmc/articles/PMC3068700/ /pubmed/20724388 http://dx.doi.org/10.1099/mic.0.039255-0 Text en Copyright © 2010, SGM |
spellingShingle | Cell and Molecular Biology of Microbes Palmer, Jonathan M. Mallaredy, Sandeep Perry, Dustin W. Sanchez, James F. Theisen, Jeffrey M. Szewczyk, Edyta Oakley, Berl R. Wang, Clay C. C. Keller, Nancy P. Mirabito, Peter M. Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans |
title | Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans |
title_full | Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans |
title_fullStr | Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans |
title_full_unstemmed | Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans |
title_short | Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans |
title_sort | telomere position effect is regulated by heterochromatin-associated proteins and nkua in aspergillus nidulans |
topic | Cell and Molecular Biology of Microbes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068700/ https://www.ncbi.nlm.nih.gov/pubmed/20724388 http://dx.doi.org/10.1099/mic.0.039255-0 |
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