Molecular Biology and Evolution, Vol 16, 253-265, Copyright © 1999 by Society for Molecular Biology and Evolution
JM Hancock, PJ Shaw, F Bonneton and GA Dover
Extensive sequence analysis of the developmental gene hunchback and its 5'
and 3' regulatory regions in Drosophila melanogaster, Drosophila virilis,
Musca domestica, and Tribolium castaneum, using a variety of computer
algorithms, reveals regions of high sequence simplicity probably generated
by slippage-like mechanisms of turnover. No regions are entirely refractory
to the action of slippage, although the density and composition of simple
sequence motifs varies from region to region. Interestingly, the 5' and 3'
flanking regions share short repetitive motifs despite their separation by
the gene itself, and the motifs are different in composition from those in
the exons and introns. Furthermore, there are high levels of conservation
of motifs in equivalent orthologous regions. Detailed sequence analysis of
the P2 promoter and DNA footprinting assays reveal that the number,
orientation, sequence, spacing, and protein-binding affinities of the
BICOID-binding sites varies between species and that the 'P2' promoter, the
nanos response element in the 3' untranslated region, and several conserved
boxes of sequence in the gene (e.g., the two zinc-finger regions) are
surrounded by cryptically-simple-sequence DNA. We argue that high sequence
turnover and genetic redundancy permit both the general maintenance of
promoter functions through the establishment of coevolutionary
(compensatory) changes in cis- and trans-acting genetic elements and, at
the same time, the possibility of subtle changes in the regulation of
hunchback in the different species.
ORIGINAL ARTICLE
High sequence turnover in the regulatory regions of the developmental gene hunchback in insects
MRC Clinical Sciences Centre, Hammersmith Hospital, London, England.
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