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First published online July 21, 2003
doi: 10.1242/10.1242/dev.00611
Department of Biology, Duke University, Durham, NC 27708, USA
* Author for correspondence (e-mail: gwray{at}duke.edu)
Accepted 24 April 2003
Evolutionary changes in transcriptional regulation undoubtedly play an
important role in creating morphological diversity. However, there is little
information about the evolutionary dynamics of cis-regulatory sequences. This
study examines the functional consequence of evolutionary changes in the
Endo16 promoter of sea urchins. The Endo16 gene encodes a
large extracellular protein that is expressed in the endoderm and may play a
role in cell adhesion. Its promoter has been characterized in exceptional
detail in the purple sea urchin, Strongylocentrotus purpuratus. We
have characterized the structure and function of the Endo16 promoter
from a second sea urchin species, Lytechinus variegatus. The
Endo16 promoter sequences have evolved in a strongly mosaic manner
since these species diverged
35 million years ago: the most proximal
region (module A) is conserved, but the remaining modules (B-G) are
unalignable. Despite extensive divergence in promoter sequences, the pattern
of Endo16 transcription is largely conserved during embryonic and
larval development. Transient expression assays demonstrate that 2.2 kb of
upstream sequence in either species is sufficient to drive GFP reporter
expression that correctly mimics this pattern of Endo16
transcription. Reciprocal cross-species transient expression assays imply that
changes have also evolved in the set of transcription factors that interact
with the Endo16 promoter. Taken together, these results suggest that
stabilizing selection on the transcriptional output may have operated to
maintain a similar pattern of Endo16 expression in S.
purpuratus and L. variegatus, despite dramatic divergence in
promoter sequence and mechanisms of transcriptional regulation.
Key words: Echinoderm, Endo16, Evolution, Promoter, Sea urchin, Transcription
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