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First published online 3 July 2006
doi: 10.1242/dev.02451


Development 133, 2983-2993 (2006)
Published by The Company of Biologists 2006


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Dissecting the regulatory landscape of the Abd-B gene of the bithorax complex

Jozsef Mihaly1, Stéphane Barges2, Laszlo Sipos1, Robert Maeda2, Fabienne Cléard2, Ilham Hogga2, Welcome Bender3, Henrik Gyurkovics1 and François Karch2,*

1 Institute of Genetics, Biological Research Center, Hungarian Academy of Sciences, 6723 Szeged, Hungary.
2 Department of Zoology and Animal Biology and National Research Centre `Frontiers in Genetics', University of Geneva, 30 quai E. Ansermet, 1211 Geneva-4, Switzerland.
3 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

* Author for correspondence (e-mail: francois.karch{at}zoo.unige.ch)

Accepted 22 May 2006

The three homeotic genes of the bithorax complex (BX-C), Ubx, abd-A and Abd-B control the identity of the posterior thorax and all abdominal segments. Large segment-specific cis-regulatory regions control the expression of Ubx, abd-A or Abd-B in each of the segments. These segment-specific cis-regulatory regions span the whole 300 kb of the BX-C and are arranged on the chromosome in the same order as the segments they specify. Experiments with lacZ reporter constructs revealed the existence of several types of regulatory elements in each of the cis-regulatory regions. These include initiation elements, maintenance elements, cell type- or tissue-specific enhancers, chromatin insulators and the promoter targeting sequence. In this paper, we extend the analysis of regulatory elements within the BX-C by describing a series of internal deficiencies that affect the Abd-B regulatory region. Many of the elements uncovered by these deficiencies are further verified in transgenic reporter assays. Our results highlight four key features of the iab-5, iab-6 and iab-7 cis-regulatory region of Abd-B. First, the whole Abd-B region is modular by nature and can be divided into discrete functional domains. Second, each domain seems to control specifically the level of Abd-B expression in only one parasegment. Third, each domain is itself modular and made up of a similar set of definable regulatory elements. And finally, the activity of each domain is absolutely dependent on the presence of an initiator element.

Key words: Bithorax, Hox gene, Abd-B, Chromatin boundary, Insulator, PRE, PTS, Drosophila


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