Title of article
Genome-wide Analysis Reveals MOF as a Key Regulator of Dosage Compensation and Gene Expression in Drosophila
Author/Authors
Jop Kind، نويسنده , , Juan M. Vaquerizas، نويسنده , , Philipp Gebhardt، نويسنده , , Marc Gentzel، نويسنده , , Nicholas M. Luscombe، نويسنده , , Paul Bertone، نويسنده , , Asifa Akhtar، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2008
Pages
16
From page
813
To page
828
Abstract
Dosage compensation, mediated by the MSL complex, regulates X-chromosomal gene expression in Drosophila. Here we report that the histone H4 lysine 16 (H4K16) specific histone acetyltransferase MOF displays differential binding behavior depending on whether the target gene is located on the X chromosome versus the autosomes. More specifically, on the male X chromosome, where MSL1 and MSL3 are preferentially associated with the 3′ end of dosage compensated genes, MOF displays a bimodal distribution binding to promoters and the 3′ ends of genes. In contrast, on MSL1/MSL3 independent X-linked genes and autosomal genes in males and females, MOF binds primarily to promoters. Binding of MOF to autosomes is functional, as H4K16 acetylation and the transcription levels of a number of genes are affected upon MOF depletion. Therefore, MOF is not only involved in the onset of dosage compensation, but also acts as a regulator of gene expression in the Drosophila genome.
Journal title
CELL
Serial Year
2008
Journal title
CELL
Record number
1019268
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