First published online March 7, 2005
Development 132, 704e (2005)
© The Company of Biologists Limited
Evolving the finding and binding of Hox targets
Hox proteins are transcriptional regulators that specify segmental identity
along the anteroposterior axis of multicellular animals. In
Drosophila, Hox proteins bind to DNA in association with the
Extradenticle (Exd) and Homothorax (Hth) co-factors. The Hox DNA-binding
selectivity model proposes that distinct Hox/Exd/Hth complexes select
different consensus DNA-binding sites to initiate different developmental
programs. On p. 1591,
Ebner and colleagues question this model. By screening the Drosophila
genome for the consensus Lab/Exd/Hth-binding sequence, the authors have
discovered a new target gene regulated by the Hox protein Labial (Lab).
Surprisingly, the regulation of this gene by Lab does not depend on the
Lab/Exd-binding consensus site but on a strongly divergent sequence. The
researchers conclude that more complexity needs to be built into the Hox
DNA-binding selectivity model to accommodate their findings. On
p. 1567, Hersh and
Carroll consider how Hox genes regulate development from an evolutionary point
of view. The researchers identify the knot gene as a direct target of
the Hox protein Ultrabithorax (Ubx) in the developing Drosophila
haltere and find that the minimal element for knot repression by Ubx
is not conserved between Drosophila species. They conclude that Hox
cis-regulatory regions, the evolutionary selection of which underlies how Hox
proteins direct the production of different metazoan body forms, are more
diffuse and larger than previously thought.

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