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Dosage compensation: an intertwined world of RNA and chromatin remodelling
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Dosage compensation: an intertwined world of RNA and chromatin remodelling
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
main subject
dosage compensation complex assembly
1 reference
stated in
Gene Ontology release 2020-05-02
Gene Ontology ID
GO:0042714
dosage compensation complex assembly involved in dosage compensation by hypoactivation of X chromosome
1 reference
stated in
Gene Ontology release 2020-05-02
Gene Ontology ID
GO:0042715
author name string
Asifa Akhtar
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
publication date
1 April 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
published in
Current Opinion in Genetics & Development
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
volume
13
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
page(s)
161-169
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stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
cites work
Gene action in the X-chromosome of the mouse (Mus musculus L.)
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Caenorhabditis elegans compensates for the difference in X chromosome dosage between the sexes by regulating transcript levels
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Synthesis of ribonucleic acid by the X-chromosomes of Drosophila melanogaster and the problem of dosage compensation.
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Histone H4 isoforms acetylated at specific lysine residues define individual chromosomes and chromatin domains in Drosophila polytene nuclei
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Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation
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Histone H3 lysine 9 methylation occurs rapidly at the onset of random X chromosome inactivation.
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Regulation of the different chromatin states of autosomes and X chromosomes in the germ line of C. elegans
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Control of X chromosome transcription by the maleless gene in Drosophila.
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Expression of msl-2 causes assembly of dosage compensation regulators on the X chromosomes and female lethality in Drosophila
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Male-specific lethal 2, a dosage compensation gene of Drosophila, undergoes sex-specific regulation and encodes a protein with a RING finger and a metallothionein-like cysteine cluster.
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The maleless protein associates with the X chromosome to regulate dosage compensation in drosophila
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mof, a putative acetyl transferase gene related to the Tip60 and MOZ human genes and to the SAS genes of yeast, is required for dosage compensation in Drosophila
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Genes expressed in neurons of adult male Drosophila
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The rox1 and rox2 RNAs are essential components of the compensasome, which mediates dosage compensation in Drosophila
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roX1 RNA paints the X chromosome of male Drosophila and is regulated by the dosage compensation system
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JIL-1, a chromosomal kinase implicated in regulation of chromatin structure, associates with the male specific lethal (MSL) dosage compensation complex
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Acetylated histone H4 on the male X chromosome is associated with dosage compensation in Drosophila
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Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila.
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Dosage compensation and chromatin structure in Drosophila
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Epigenetic spreading of the Drosophila dosage compensation complex from roX RNA genes into flanking chromatin.
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Ordered assembly of roX RNAs into MSL complexes on the dosage-compensated X chromosome in Drosophila
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Linking global histone acetylation to the transcription enhancement of X-chromosomal genes in Drosophila males
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Association and spreading of the Drosophila dosage compensation complex from a discrete roX1 chromatin entry site.
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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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RNA-dependent association of the Drosophila maleless protein with the male X chromosome.
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Chromodomains are protein-RNA interaction modules
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The roX genes encode redundant male-specific lethal transcripts required for targeting of the MSL complex
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Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi
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Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1alpha
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Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component
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Cooperation between complexes that regulate chromatin structure and transcription
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The ISWI chromatin-remodeling protein is required for gene expression and the maintenance of higher order chromatin structure in vivo
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Modulation of ISWI function by site-specific histone acetylation
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The histone H4 acetyltransferase MOF uses a C2HC zinc finger for substrate recognition
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The Isw2 chromatin remodeling complex represses early meiotic genes upon recruitment by Ume6p
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Widespread collaboration of Isw2 and Sin3-Rpd3 chromatin remodeling complexes in transcriptional repression
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Dosage-dependent gene regulation in multicellular eukaryotes: implications for dosage compensation, aneuploid syndromes, and quantitative traits
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900016-9
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7 January 2021
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JIL-1: a novel chromosomal tandem kinase implicated in transcriptional regulation in Drosophila
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900016-9
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7 January 2021
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The JIL-1 tandem kinase mediates histone H3 phosphorylation and is required for maintenance of chromatin structure in Drosophila.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900016-9
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Recruitment of the male-specific lethal (MSL) dosage compensation complex to an autosomally integrated roX chromatin entry site correlates with an increased expression of an adjacent reporter gene in male Drosophila
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900016-9
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Chromosomal silencing and localization are mediated by different domains of Xist RNA.
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900016-9
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X-chromosome inactivation and the search for chromosome-wide silencers
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X-chromosome inactivation: counting, choice and initiation
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X-chromosome inactivation: closing in on proteins that bind Xist RNA.
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https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900016-9
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Imprinted X inactivation maintained by a mouse Polycomb group gene
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Mitotically stable association of polycomb group proteins eed and enx1 with the inactive x chromosome in trophoblast stem cells
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Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome
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BRCA1 supports XIST RNA concentration on the inactive X chromosome
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A new human member of the MYST family of histone acetyl transferases with high sequence similarity to Drosophila MOF
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Origin and evolution of the regulatory gene male-specific lethal-3.
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MSL1 plays a central role in assembly of the MSL complex, essential for dosage compensation in Drosophila
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The drosophila MSL complex acetylates histone H4 at lysine 16, a chromatin modification linked to dosage compensation
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Identifiers
DOI
10.1016/S0959-437X(03)00016-9
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
PubMed ID
12672493
1 reference
stated in
Europe PubMed Central
PubMed ID
12672493
retrieved
6 August 2017
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