Premium
MSL1 plays a central role in assembly of the MSL complex, essential for dosage compensation in Drosophila
Author(s) -
Scott Maxwell J.,
Pan Lewis L.,
Cleland Sheralee B.,
Knox Andrea L.,
Heinrich Jörg
Publication year - 2000
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/19.1.144
Subject(s) - biology , dosage compensation , drosophila (subgenus) , compensation (psychology) , drosophila melanogaster , evolutionary biology , genetics , microbiology and biotechnology , gene , gene expression , psychology , psychoanalysis
In male Drosophila , histone H4 acetylated at Lys16 is enriched on the X chromosome, and most X‐linked genes are transcribed at a higher rate than in females (thus achieving dosage compensation). Five proteins, collectively called the MSLs, are required for dosage compensation and male viability. Here we show that one of these proteins, MSL1, interacts with three others, MSL2, MSL3 and MOF. The latter is a putative histone acetyl transferase. Overexpression of either the N‐ or C‐terminal domain of MSL1 has dominant‐negative effects, i.e. causes male‐specific lethality. The lethality due to expression of the N‐terminal domain is reduced if msl2 is co‐overexpressed. MSL2 co‐purifies over a FLAG affinity column with the tagged region of MSL1, and both MSL3 and MOF co‐purify with the FLAG‐tagged MSL1 C‐terminal domain. Furthermore, the MSL1 C‐terminal domain binds specifically to a GST–MOF fusion protein and co‐immunoprecipitates with HA‐tagged MSL3. The MSL1 C‐terminal domain shows similarity to a region of mouse CBP, a transcription co‐activator. We conclude that a main role of MSL1 is to serve as the backbone for assembly of the MSL complex.