Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.

Co-evolution of transcriptional regulatory proteins and their sites of action has been often hypothesized but rarely demonstrated. Here we provide experimental evidence of such co-evolution in yeast silent chromatin, a finding that emerged from studies of hybrids formed between two closely related S...

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Main Authors: Oliver A Zill, Devin Scannell, Leonid Teytelman, Jasper Rine
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-11-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC2994660?pdf=render
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spelling doaj-773c08bfcc094af38bae9e895e9e628f2021-07-02T13:42:33ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852010-11-01811e100055010.1371/journal.pbio.1000550Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.Oliver A ZillDevin ScannellLeonid TeytelmanJasper RineCo-evolution of transcriptional regulatory proteins and their sites of action has been often hypothesized but rarely demonstrated. Here we provide experimental evidence of such co-evolution in yeast silent chromatin, a finding that emerged from studies of hybrids formed between two closely related Saccharomyces species. A unidirectional silencing incompatibility between S. cerevisiae and S. bayanus led to a key discovery: asymmetrical complementation of divergent orthologs of the silent chromatin component Sir4. In S. cerevisiae/S. bayanus interspecies hybrids, ChIP-Seq analysis revealed a restriction against S. cerevisiae Sir4 associating with most S. bayanus silenced regions; in contrast, S. bayanus Sir4 associated with S. cerevisiae silenced loci to an even greater degree than did S. cerevisiae's own Sir4. Functional changes in silencer sequences paralleled changes in Sir4 sequence and a reduction in Sir1 family members in S. cerevisiae. Critically, species-specific silencing of the S. bayanus HMR locus could be reconstituted in S. cerevisiae by co-transfer of the S. bayanus Sir4 and Kos3 (the ancestral relative of Sir1) proteins. As Sir1/Kos3 and Sir4 bind conserved silencer-binding proteins, but not specific DNA sequences, these rapidly evolving proteins served to interpret differences in the two species' silencers presumably involving emergent features created by the regulatory proteins that bind sequences within silencers. The results presented here, and in particular the high resolution ChIP-Seq localization of the Sir4 protein, provided unanticipated insights into the mechanism of silent chromatin assembly in yeast.http://europepmc.org/articles/PMC2994660?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Oliver A Zill
Devin Scannell
Leonid Teytelman
Jasper Rine
spellingShingle Oliver A Zill
Devin Scannell
Leonid Teytelman
Jasper Rine
Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
PLoS Biology
author_facet Oliver A Zill
Devin Scannell
Leonid Teytelman
Jasper Rine
author_sort Oliver A Zill
title Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
title_short Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
title_full Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
title_fullStr Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
title_full_unstemmed Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
title_sort co-evolution of transcriptional silencing proteins and the dna elements specifying their assembly.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2010-11-01
description Co-evolution of transcriptional regulatory proteins and their sites of action has been often hypothesized but rarely demonstrated. Here we provide experimental evidence of such co-evolution in yeast silent chromatin, a finding that emerged from studies of hybrids formed between two closely related Saccharomyces species. A unidirectional silencing incompatibility between S. cerevisiae and S. bayanus led to a key discovery: asymmetrical complementation of divergent orthologs of the silent chromatin component Sir4. In S. cerevisiae/S. bayanus interspecies hybrids, ChIP-Seq analysis revealed a restriction against S. cerevisiae Sir4 associating with most S. bayanus silenced regions; in contrast, S. bayanus Sir4 associated with S. cerevisiae silenced loci to an even greater degree than did S. cerevisiae's own Sir4. Functional changes in silencer sequences paralleled changes in Sir4 sequence and a reduction in Sir1 family members in S. cerevisiae. Critically, species-specific silencing of the S. bayanus HMR locus could be reconstituted in S. cerevisiae by co-transfer of the S. bayanus Sir4 and Kos3 (the ancestral relative of Sir1) proteins. As Sir1/Kos3 and Sir4 bind conserved silencer-binding proteins, but not specific DNA sequences, these rapidly evolving proteins served to interpret differences in the two species' silencers presumably involving emergent features created by the regulatory proteins that bind sequences within silencers. The results presented here, and in particular the high resolution ChIP-Seq localization of the Sir4 protein, provided unanticipated insights into the mechanism of silent chromatin assembly in yeast.
url http://europepmc.org/articles/PMC2994660?pdf=render
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