Structural basis for MOF and MSL3 recruitment into the dosage compensation complex by MSL1

被引：0
|
作者：
Jan Kadlec
Erinc Hallacli
Michael Lipp
Herbert Holz
Juan Sanchez-Weatherby
Stephen Cusack
Asifa Akhtar
机构：
[1] European Molecular Biology Laboratory,
[2] Unit of Virus Host-Cell Interactions,undefined
[3] Université Joseph Fouier–European Molecular Biology Laboratory–Centre National de la Recherche Scientifique (UJF-EMBL-CNRS),undefined
[4] Unité Mixte Internationale 3265,undefined
[5] European Molecular Biology Laboratory,undefined
[6] Present addresses: Max-Planck-Institut für Immunbiologie und Epigenetik,undefined
[7] Freiburg im Breisgau,undefined
[8] Germany (E.H.,undefined
[9] H.H.,undefined
[10] A.A.); Diamond Light Source Ltd.,undefined
[11] Didcot,undefined
[12] UK (J.S.-W.).,undefined
来源：
Nature Structural & Molecular Biology | 2011年 / 18卷
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摘要：
In Drosophila, upregulation of genes on the single male X chromosome to match that from the two female Xs depends upon the MSL complex. The structures of complexes of MSL subunits now give insight into how the MOF histone acetyltransferase and MSL3 interact with MSL1, indicating that the latter acts as a scaffold to bring the complex together.
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页码：142 / 149
页数：7
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