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Eanes Lab
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Projects
Insect Flight
We used P-element excision-derived knockouts in Drosophila melanogaster to experimentally lower the in vivo activity levels of seven enzymes in this pathway and examine individual enzyme influence on tethered flight performance measured as wing beat frequency (WBF) under high speed video and ability to sustain free flight (Flowers et al. 2006). Our results find the classic regulatory enzyme, glycogen phosphorylase, is nearest to capacity or saturation, while other enzymes, especially those termed near-equilibrium, possess excess capacity. These latter enzymes show extreme genetic dominance and low flux control that extends down to markedly reduced enzyme levels. The genetic results are generally consistent with physiological studies using in vitro estimates that predict near-equilibrium enzymes carry excess capacity. The possibility is that this excess capacity is exploited under demand states different from the experimental test conditions. I have an NSF-sponsored three year project (2009-2012) to continue these studies. This study will continue to study metabolic flight performance. examines the rate-limiting steps involved in pathway control (if any), and determines if there are differences in degree of saturation or excess capacity for different steps. These experiments test if this activity is drawn upon under conditions (temperature and load demands) requiring reserve capacity (formally these are genotype-by-environmental interactions). It will also explore the effects of gene-gene interactions (epistasis) on flight performance, and determines (1) if dominance can be modified by genetic background change, and (2) if dominance modification depends on the nature of mechanistic interrelationships between enzyme steps. Reproductive Diapause
We
have mapped the genetic variation in this trait to a specific gene (the couch
potato gene) and a single amino acid polymorphism that shows a parallel
geographic cline with diapause (Schmidt et al. 2008). I have a joint NSF-sponsored
three year grant (2009-2012) with Paul Schmidt
at the University of Pennsylvania to
further study cpo and its functional role in the establishment of diapause. The
project will examine the functional significance and adaptive dynamics of the cpo462Ile/Lys
polymorphism in natural populations. It will explore the global molecular
population genetics of the cpo
gene region and extend our analyses to ancestral African populations as well as
derived populations on other continents. We plan to identify modifiers of
diapause outside the third chromosome and to examine the interaction between cpo
and pathways known to affect life histories in Drosophila. To perform an initial
examination of the mechanism by which cpo
determines diapause and associated life histories. Energy-sensing
A
common statement is that “nutrient sensors” or “sensory neurons”
initiate these signaling processes. These specialized cells sense the energy
state via the levels of metabolites. Since
the downstream signaling systems appear highly conserved in metazoans, we
propose that these upstream sensors are conserved as well. However, other than
the insulin secretion in mammals, very little is known in any model
species about the nutrient or metabolic energy-state sensors residing at the
very top that initiate signaling, or
how genetic variation in these sensors is involved in adaptation to
environmental change. This project in collaboration with the lab of John True examines the extent to which nutrient signaling mechanisms are conserved between flies and mammals and examine Drosophila as a suitable model for understanding these mechanisms.
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