A plasmid model system shows that Drosophila dosage compensation depends on the global acetylation of histone H4 at lysine 16 and is not affected by depletion of common transcription elongation chromatin marks (Q36315870)

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English	A plasmid model system shows that Drosophila dosage compensation depends on the global acetylation of histone H4 at lysine 16 and is not affected by depletion of common transcription elongation chromatin marks	scientific article

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PMC publication ID

2169142

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13 August 2017

title

A plasmid model system shows that Drosophila dosage compensation depends on the global acetylation of histone H4 at lysine 16 and is not affected by depletion of common transcription elongation chromatin marks (English)

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PMC publication ID

2169142

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13 August 2017

main subject

Drosophila

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author name string

Ruth Yokoyama

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1

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Europe PubMed Central

PMC publication ID

2169142

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13 August 2017

Antonio Pannuti

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2

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PMC publication ID

2169142

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13 August 2017

Huiping Ling

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3

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Europe PubMed Central

PMC publication ID

2169142

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13 August 2017

Edwin R Smith

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4

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Europe PubMed Central

PMC publication ID

2169142

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13 August 2017

John C Lucchesi

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5

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PMC publication ID

2169142

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13 August 2017

language of work or name

English

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publication date

17 September 2007

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2169142

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13 August 2017

number of pages

6

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Molecular and Cellular Biology

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Europe PubMed Central

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2169142

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13 August 2017

volume

27

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Europe PubMed Central

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2169142

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13 August 2017

issue

22

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Europe PubMed Central

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2169142

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13 August 2017

page(s)

7865-7870

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2169142

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13 August 2017

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ImageJ

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Europe PubMed Central

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11 June 2022

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https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2169142/fullTextXML

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cites work

MES-4: an autosome-associated histone methyltransferase that participates in silencing the X chromosomes in the C. elegans germ line.

1 reference

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PubMed Central

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30 September 2017

Breaking barriers to transcription elongation

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

High-resolution ChIP-chip analysis reveals that the Drosophila MSL complex selectively identifies active genes on the male X chromosome

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

Chromosome-wide gene-specific targeting of the Drosophila dosage compensation complex

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PubMed Central

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30 September 2017

Histone H4-K16 acetylation controls chromatin structure and protein interactions

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

Eaf3 chromodomain interaction with methylated H3-K36 links histone deacetylation to Pol II elongation

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PubMed Central

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30 September 2017

Drosophila Paf1 modulates chromatin structure at actively transcribed genes.

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PubMed Central

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30 September 2017

Cotranscriptional set2 methylation of histone H3 lysine 36 recruits a repressive Rpd3 complex

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PubMed Central

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30 September 2017

Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcription

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PubMed Central

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30 September 2017

Chromatin remodeling in dosage compensation

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PubMed Central

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30 September 2017

Distinction and relationship between elongation rate and processivity of RNA polymerase II in vivo

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PubMed Central

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30 September 2017

Histone H3.3 is enriched in covalent modifications associated with active chromatin

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

Probing chromatin immunoprecipitates with CpG-island microarrays to identify genomic sites occupied by DNA-binding proteins

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PubMed Central

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30 September 2017

Male-specific lethal complex of Drosophila targets activated regions of the X chromosome for chromatin remodeling

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

Drosophila FACT contributes to Hox gene expression through physical and functional interactions with GAGA factor

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PubMed Central

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30 September 2017

Solvent mediated interactions in the structure of the nucleosome core particle at 1.9 a resolution

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PubMed Central

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30 September 2017

The drosophila MSL complex acetylates histone H4 at lysine 16, a chromatin modification linked to dosage compensation

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

Light-dependent sequestration of TIMELESS by CRYPTOCHROME

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PubMed Central

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30 September 2017

Crystal structure of the nucleosome core particle at 2.8 A resolution

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

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30 September 2017

The Drosophila EcR gene encodes an ecdysone receptor, a new member of the steroid receptor superfamily

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PubMed Central

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30 September 2017

The complex set of late transcripts from the Drosophila sex determination gene sex-lethal encodes multiple related polypeptides

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PubMed Central

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30 September 2017

Tight control of gene expression in mammalian cells by tetracycline-responsive promoters

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PubMed Central

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30 September 2017

Sex lethal controls dosage compensation in Drosophila by a non-splicing mechanism

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PubMed Central

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29 June 2018

The RNA polymerase II kinase Ctk1 regulates positioning of a 5' histone methylation boundary along genes.

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22 September 2018

Genome-scale profiling of histone H3.3 replacement patterns.

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PubMed Central

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22 September 2018

Linking global histone acetylation to the transcription enhancement of X-chromosomal genes in Drosophila males

1 reference

stated in

PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169142

retrieved

22 September 2018

Identifiers

DOI

10.1128/MCB.00397-07

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stated in

Europe PubMed Central

PMC publication ID

2169142

retrieved

13 August 2017

PMC publication ID

2169142

1 reference

stated in

Europe PubMed Central

PMC publication ID

2169142

retrieved

13 August 2017

PubMed publication ID

17875941

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Europe PubMed Central

PMC publication ID

2169142

retrieved

13 August 2017

ResearchGate publication ID

5966980

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