FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Dunlap, D., Yokoyama, R., Ling, H., Sun, H.Y., McGill, K., Cugusi, S., Lucchesi, J.C. (2012). Distinct contributions of MSL complex subunits to the transcriptional enhancement responsible for dosage compensation in Drosophila.  Nucleic Acids Res. 40(22): 11281--11291.
FlyBase ID
FBrf0220258
Publication Type
Research paper
Abstract
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.
PubMed ID
PubMed Central ID
PMC3526317 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nucleic Acids Res.
    Title
    Nucleic Acids Research
    Publication Year
    1974-
    ISBN/ISSN
    0305-1048
    Data From Reference
    Genes (12)