DESCRIPTION (provided by applicant): Through comparative studies between
distantly related animals, it has become apparent that genes and regulatory
networks functioning during embryonic growth are highly conserved. This has led
to the hypothesis that evolutionary changes in morphology can be traced to
alterations in these regulatory modules. Studies to address this hypothesis
have focused on insects, which display different modes of segmentation. Most
approaches rely on cloning and expression analysis of orthologs of
well-characterized Drosophila genes. However, most insects do not offer facile
approaches to examine the functional significance of conserved gene expression
patterns, or to test observed differences. Further, these comparisons are
limited to the analysis of mechanisms discovered in flies, and do not offer the
possibility of identifying genes important to segmentation in species other
than flies. Our studies in Tribolium overcome these limitations, since
Tribolium offers the possibility of genetic manipulation in addition to its
facility for developmental and molecular studies. Moreover, the recent advances
in RNA interference and germline transformation place Tribolium in the
forefront of comparative model systems.
We have discovered that depletion of certain pair-rule gene mRNAs by RNAi
blocks segmentation and morphogenesis in Tribolium, results not predicted by
the Drosophila paradigm. To understand the molecular interaction underlying
these novel phenotypes we will examine the effects of Tceve and Tcrun mRNA
depletion on the expression of other segmentation and homeotic genes. Analysis
of the regulatory regions associated with these genes and ectopic expression of
transgenes will complement the RNAi studies. To discover other genes important
to segmentation in Tribolium we will execute a transposon-tagging mutagenesis
scheme and characterize relevant mutants. Our research provides a unique
opportunity to elucidate the genetic mechanisms underlying the regulation of
the process of progressive segmentation in a cellular environment.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
865
DUNS Number
929773554
UEI
CFMMM5JM7HJ9
Project Start Date
01-August-1992
Project End Date
31-July-2007
Budget Start Date
01-August-2003
Budget End Date
31-July-2004
Project Funding Information for 2003
Total Funding
$290,543
Direct Costs
$202,500
Indirect Costs
$88,043
Year
Funding IC
FY Total Cost by IC
2003
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$290,543
Year
Funding IC
FY Total Cost by IC
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