H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases

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H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases. / Hansen, Klavs R; Hazan, Idit; Shanker, Sreenath; Watt, Stephen; Hansen, Janne Verhein; Bähler, Jürg; Martienssen, Robert A; Partridge, Janet F; Cohen, Amikam; Thon, Genevieve.

In: P L o S Genetics, Vol. 7, No. 1, 2011.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, KR, Hazan, I, Shanker, S, Watt, S, Hansen, JV, Bähler, J, Martienssen, RA, Partridge, JF, Cohen, A & Thon, G 2011, 'H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases', P L o S Genetics, vol. 7, no. 1. https://doi.org/10.1371/journal.pgen.1001268

APA

Hansen, K. R., Hazan, I., Shanker, S., Watt, S., Hansen, J. V., Bähler, J., Martienssen, R. A., Partridge, J. F., Cohen, A., & Thon, G. (2011). H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases. P L o S Genetics, 7(1). https://doi.org/10.1371/journal.pgen.1001268

Vancouver

Hansen KR, Hazan I, Shanker S, Watt S, Hansen JV, Bähler J et al. H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases. P L o S Genetics. 2011;7(1). https://doi.org/10.1371/journal.pgen.1001268

Author

Hansen, Klavs R ; Hazan, Idit ; Shanker, Sreenath ; Watt, Stephen ; Hansen, Janne Verhein ; Bähler, Jürg ; Martienssen, Robert A ; Partridge, Janet F ; Cohen, Amikam ; Thon, Genevieve. / H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases. In: P L o S Genetics. 2011 ; Vol. 7, No. 1.

Bibtex

@article{1aa7d19c77474973b03b52252e70e0a1,
title = "H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases",
abstract = "Nucleosomes in heterochromatic regions bear histone modifications that distinguish them from euchromatic nucleosomes. Among those, histone H3 lysine 9 methylation (H3K9me) and hypoacetylation have been evolutionarily conserved and are found in both multicellular eukaryotes and single-cell model organisms such as fission yeast. In spite of numerous studies, the relative contributions of the various heterochromatic histone marks to the properties of heterochromatin remain largely undefined. Here, we report that silencing of the fission yeast mating-type cassettes, which are located in a well-characterized heterochromatic region, is hardly affected in cells lacking the H3K9 methyltransferase Clr4. We document the existence of a pathway parallel to H3K9me ensuring gene repression in the absence of Clr4 and identify a silencing factor central to this pathway, Clr5. We find that Clr5 controls gene expression at multiple chromosomal locations in addition to affecting the mating-type region. The histone deacetylase Clr6 acts in the same pathway as Clr5, at least for its effects in the mating-type region, and on a subset of other targets, notably a region recently found to be prone to neo-centromere formation. The genomic targets of Clr5 also include Ste11, a master regulator of sexual differentiation. Hence Clr5, like the multi-functional Atf1 transcription factor which also modulates chromatin structure in the mating-type region, controls sexual differentiation and genome integrity at several levels. Globally, our results point to histone deacetylases as prominent repressors of gene expression in fission yeast heterochromatin. These deacetylases can act in concert with, or independently of, the widely studied H3K9me mark to influence gene silencing at heterochromatic loci.",
keywords = "Amino Acid Sequence, Chromosomal Proteins, Non-Histone, Gene Expression Regulation, Fungal, Gene Silencing, Heterochromatin, Histone Deacetylases, Histone-Lysine N-Methyltransferase, Histones, Methylation, Molecular Sequence Data, Mutation, Schizosaccharomyces, Schizosaccharomyces pombe Proteins, Sequence Alignment, Sequence Homology, Amino Acid, Transcription Factors",
author = "Hansen, {Klavs R} and Idit Hazan and Sreenath Shanker and Stephen Watt and Hansen, {Janne Verhein} and J{\"u}rg B{\"a}hler and Martienssen, {Robert A} and Partridge, {Janet F} and Amikam Cohen and Genevieve Thon",
note = "Artikel ID: e1001268",
year = "2011",
doi = "10.1371/journal.pgen.1001268",
language = "English",
volume = "7",
journal = "P L o S Genetics",
issn = "1553-7390",
publisher = "Public Library of Science",
number = "1",

}

RIS

TY - JOUR

T1 - H3K9me-independent gene silencing in fission yeast heterochromatin by Clr5 and histone deacetylases

AU - Hansen, Klavs R

AU - Hazan, Idit

AU - Shanker, Sreenath

AU - Watt, Stephen

AU - Hansen, Janne Verhein

AU - Bähler, Jürg

AU - Martienssen, Robert A

AU - Partridge, Janet F

AU - Cohen, Amikam

AU - Thon, Genevieve

N1 - Artikel ID: e1001268

PY - 2011

Y1 - 2011

N2 - Nucleosomes in heterochromatic regions bear histone modifications that distinguish them from euchromatic nucleosomes. Among those, histone H3 lysine 9 methylation (H3K9me) and hypoacetylation have been evolutionarily conserved and are found in both multicellular eukaryotes and single-cell model organisms such as fission yeast. In spite of numerous studies, the relative contributions of the various heterochromatic histone marks to the properties of heterochromatin remain largely undefined. Here, we report that silencing of the fission yeast mating-type cassettes, which are located in a well-characterized heterochromatic region, is hardly affected in cells lacking the H3K9 methyltransferase Clr4. We document the existence of a pathway parallel to H3K9me ensuring gene repression in the absence of Clr4 and identify a silencing factor central to this pathway, Clr5. We find that Clr5 controls gene expression at multiple chromosomal locations in addition to affecting the mating-type region. The histone deacetylase Clr6 acts in the same pathway as Clr5, at least for its effects in the mating-type region, and on a subset of other targets, notably a region recently found to be prone to neo-centromere formation. The genomic targets of Clr5 also include Ste11, a master regulator of sexual differentiation. Hence Clr5, like the multi-functional Atf1 transcription factor which also modulates chromatin structure in the mating-type region, controls sexual differentiation and genome integrity at several levels. Globally, our results point to histone deacetylases as prominent repressors of gene expression in fission yeast heterochromatin. These deacetylases can act in concert with, or independently of, the widely studied H3K9me mark to influence gene silencing at heterochromatic loci.

AB - Nucleosomes in heterochromatic regions bear histone modifications that distinguish them from euchromatic nucleosomes. Among those, histone H3 lysine 9 methylation (H3K9me) and hypoacetylation have been evolutionarily conserved and are found in both multicellular eukaryotes and single-cell model organisms such as fission yeast. In spite of numerous studies, the relative contributions of the various heterochromatic histone marks to the properties of heterochromatin remain largely undefined. Here, we report that silencing of the fission yeast mating-type cassettes, which are located in a well-characterized heterochromatic region, is hardly affected in cells lacking the H3K9 methyltransferase Clr4. We document the existence of a pathway parallel to H3K9me ensuring gene repression in the absence of Clr4 and identify a silencing factor central to this pathway, Clr5. We find that Clr5 controls gene expression at multiple chromosomal locations in addition to affecting the mating-type region. The histone deacetylase Clr6 acts in the same pathway as Clr5, at least for its effects in the mating-type region, and on a subset of other targets, notably a region recently found to be prone to neo-centromere formation. The genomic targets of Clr5 also include Ste11, a master regulator of sexual differentiation. Hence Clr5, like the multi-functional Atf1 transcription factor which also modulates chromatin structure in the mating-type region, controls sexual differentiation and genome integrity at several levels. Globally, our results point to histone deacetylases as prominent repressors of gene expression in fission yeast heterochromatin. These deacetylases can act in concert with, or independently of, the widely studied H3K9me mark to influence gene silencing at heterochromatic loci.

KW - Amino Acid Sequence

KW - Chromosomal Proteins, Non-Histone

KW - Gene Expression Regulation, Fungal

KW - Gene Silencing

KW - Heterochromatin

KW - Histone Deacetylases

KW - Histone-Lysine N-Methyltransferase

KW - Histones

KW - Methylation

KW - Molecular Sequence Data

KW - Mutation

KW - Schizosaccharomyces

KW - Schizosaccharomyces pombe Proteins

KW - Sequence Alignment

KW - Sequence Homology, Amino Acid

KW - Transcription Factors

U2 - 10.1371/journal.pgen.1001268

DO - 10.1371/journal.pgen.1001268

M3 - Journal article

C2 - 21253571

VL - 7

JO - P L o S Genetics

JF - P L o S Genetics

SN - 1553-7390

IS - 1

ER -

ID: 33344472