Distinct contributions of MSL complex subunits to the transcriptional enhancement responsible for dosage compensation in Drosophila

被引：15

作者：

Dunlap, David ^{[1
]}

Yokoyama, Ruth ^{[2
]}

Ling, Huiping ^{[2
]}

Sun, He-Ying ^{[2
]}

McGill, Kerry ^{[1
]}

Cugusi, Simona ^{[2
]}

Lucchesi, John C. ^{[2
]}

机构：

[1] Emory Univ, Dept Cell Biol, Atlanta, GA 30322 USA

[2] Emory Univ, Dept Biol, Atlanta, GA 30322 USA

来源：

NUCLEIC ACIDS RESEARCH | 2012年 / 40卷 / 22期

基金：

美国国家卫生研究院;

关键词：

ORDER CHROMATIN-STRUCTURE; NUCLEOSOME CORE PARTICLE; REMODELING ATPASE ISWI; H4 TAIL ACETYLATIONS; X-CHROMOSOME; IN-VIVO; HISTONE ACETYLATION; H4-K16; ACETYLATION; ANALYSIS REVEALS; GENE-EXPRESSION;

D O I：

10.1093/nar/gks890

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The regulatory mechanism of dosage compensation is the paramount example of epigenetic regulation at the chromosomal level. In Drosophila, this mechanism, designed to compensate for the difference in the dosage of X-linked genes between the sexes, depends on the MSL complex that enhances the transcription of the single dose of these genes in males. We have investigated the function of various subunits of the complex in mediating dosage compensation. Our results confirm that the highly enriched specific acetylation of histone H4 at lysine 16 of compensated genes by the histone acetyl transferase subunit MOF induces a more disorganized state of their chromatin. We have determined that the association of the MSL complex reduces the level of negative supercoiling of the deoxyribonucleic acid of compensated genes, and we have defined the role that the other subunits of the complex play in this topological modification. Lastly, we have analyzed the potential contribution of ISWI-containing remodeling complexes to the architecture of compensated chromatin, and we suggest a role for this remodeling factor in dosage compensation.

引用

页码：11281 / 11291

页数：11

共 26 条

[21] Male-specific lethal complex in Drosophila counteracts histone acetylation and does not mediate dosage compensation
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Fernandez, Harvey R.
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Li, Jilong
Cheng, Jianlin
Birchler, James A.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (09) : E808 - E817
[22] An MLL/COMPASS subunit functions in the C. elegans dosage compensation complex to target X chromosomes for transcriptional regulation of gene expression
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[23] Species-specific positive selection of the male-specific lethal complex that participates in dosage compensation in Drosophila
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (39) : 15412 - 15417
[24] Rapid Evolution of Autosomal Binding Sites of the Dosage Compensation Complex in Drosophila melanogaster and Its Association With Transcription Divergence
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FRONTIERS IN GENETICS, 2021, 12
[25] The importance of location and orientation of male specific lethal complex binding sites of differing affinities on reporter gene dosage compensation in Drosophila
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Li, Fang
Laverty, Corey
Belikoff, Esther J.
Scott, Maxwell J.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 402 (04) : 699 - 704
[26] No Evidence for a Global Male-Specific Lethal Complex-Mediated Dosage Compensation Contribution to the Demasculinization of the Drosophila melanogaster X Chromosome
Vensko, Steven P., II
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PLOS ONE, 2014, 9 (08):

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