Hit and run: X marks the spot!

Nature structural & molecular biology ·Vol. 16 ·No. 8 ·2009-08-00 ·Pages 801-3

Weake VM, Workman JL

Abstract

暂无摘要

MeSH Terms

Acetylation Animals Dosage Compensation, Genetic Drosophila Proteins/genetics,metabolism Drosophila melanogaster/genetics,metabolism Female Histone Acetyltransferases/genetics,metabolism Histones/metabolism Lysine/metabolism Male Models, Biological X Chromosome/genetics

Chemicals

Drosophila Proteins Histones Histone Acetyltransferases Lysine

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Weake Vikki M

Workman Jerry L

References (16)

16 references, click to expand

Combinatorial patterns of histone acetylations and methylations in the human genome.
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Drosophila male-specific lethal-2 protein: structure/function analysis and dependence on MSL-1 for chromosome association.
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Genome-wide analysis reveals MOF as a key regulator of dosage compensation and gene expression in Drosophila.
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MSL complex is attracted to genes marked by H3K36 trimethylation using a sequence-independent mechanism.
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The Drosophila NURF remodelling and the ATAC histone acetylase complexes functionally interact and are required for global chromosome organization.
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Nuclear pore components are involved in the transcriptional regulation of dosage compensation in Drosophila.
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Targeting the chromatin-remodeling MSL complex of Drosophila to its sites of action on the X chromosome requires both acetyl transferase and ATPase activities.
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Drosophila dosage compensation: a complex voyage to the X chromosome.
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ATAC is a double histone acetyltransferase complex that stimulates nucleosome sliding.
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Global analysis of X-chromosome dosage compensation.
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Drosophila MSL complex globally acetylates H4K16 on the male X chromosome for dosage compensation.
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Polycomb complexes and epigenetic states.
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Article Info

Journal

Nature structural & molecular biology

Abbr.

Nat Struct Mol Biol

ISSN

1545-9985

DOI

10.1038/nsmb0809-801

Published

2009-08-00

Pages

801-3

Language

English

Region

United States

NLM ID

101186374

Subset

Grants

NIGMS NIH HHS · R01 GM047867 · United States

Corrections

CommentOn

PMID: 19648925

External Links

PubMed source DOI: 10.1038/nsmb0809-801 View journal details

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