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Nucleic Acids Research Advance Access published online on May 5, 2007

Nucleic Acids Research, doi:10.1093/nar/gkm282
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© 2007 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Molecular Biology

Cumulative contributions of weak DNA determinants to targeting the Drosophila dosage compensation complex

Gregor D. Gilfillan, Cornelia König, Ina K. Dahlsveen, Nicky Prakoura, Tobias Straub, Rosemarie Lamm, Torsten Fauth and Peter B. Becker*

Adolf-Butenandt Institut, Molekularbiologie, Ludwig Maximilian Universität, Schillerstrasse 44, 80336 Munich, Germany

*To whom correspondence should be addressed. Tel: +49-89-2180-75427; Fax: +49-89-2180-75425; Email: pbecker{at}med.uni-muenchen.de

Received February 20, 2007. Revised April 11, 2007. Accepted April 11, 2007.

Fine-tuning of X chromosomal gene expression in Drosophila melanogaster involves the selective interaction of the Dosage Compensation Complex (DCC) with the male X chromosome, in order to increase the transcription of many genes. However, the X chromosomal DNA sequences determining DCC binding remain elusive. By adapting a ‘one-hybrid’ assay, we identified minimal DNA elements that direct the interaction of the key DCC subunit, MSL2, in cells. Strikingly, several such novel MSL2 recruitment modules have very different DNA sequences. The assay revealed a novel, 40 bp DNA element that is necessary for recruitment of DCC to an autosomal binding site in flies in the context of a longer sequence and sufficient by itself to direct recruitment if trimerized. Accordingly, recruitment of MSL2 to the single 40 bp element in cells was weak, but as a trimer approached the power of the strongest DCC recruitment site known to date, the roX1 DH site. This element is the shortest MSL2 recruitment sequence known to date. The results support a model for MSL2 recruitment according to which several different, degenerate sequence motifs of variable affinity cluster and synergise to form a high affinity site.


Present addresses: Gregor D. Gilfillan, Ullevål Universitetssykehus, Medisinsk Genetikk, Kirkeveien 166, 0407 Oslo, Norway Cornelia König, Zentrum für Molekulare Biologie Heidelberg (ZMBH), Im Neuenheimer Feld 282, University Heidelberg, 69120 Heidelberg, Germany

Ina K. Dahlsveen, Exiqon A/S, Bygstubben 9, DK-2950 Vedbaek, Denmark


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