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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...

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Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Microbiology Society 2010
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.
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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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