ハングオーバーはNSLを介したH4K16アセチル化を制限することにより遺伝子発現を調節する
Jonathan Lenz1, Laura Schmelzer1,2, Ignasi Forné3
1Institute of Molecular Biology and Tumor Research, Faculty of Medicine, Philipps-Universität Marburg, Marburg 35043, Germany.
Abstract:
The RNA-binding protein Hangover (Hang) is essential for several stress responses in Drosophila melanogaster. Here, we discover a novel function of Hang in the regulation of gene expression. Hang binds to >2000 genes in the Drosophila genome and modulates transcription. We identify a diverse set of chromatin regulators as Hang interactors, including NSL, dMec, Sin3A, dREAM, and Ino80. Among these, the non-specific lethal complex (NSL) is the most prominent one. We show that Hang attenuates NSL-mediated H4K16 acetylation at transcriptional start sites to downregulate gene expression. Our work uncovers novel roles for Hang in epigenetic gene regulation and suggests that it coordinates the function of multiple chromatin regulators.
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関連する概念動画
Histone Modification
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
Histone Modification
Cell Specific Gene Expression
Chromatin Structure Regulates pre-mRNA Processing
The chromatin structure, especially...
Transcription Attenuation in Prokaryotes
There are several different mechanisms used to attenuate transcription. In ribosome mediated...
Regulation of Expression at Multiple Steps
