Molecular analysis of olfactory perception in Drosophila melanogaster
Abstract
Over the last decade the insect olfactory system has emerged as
an important model
system with which to investigate the biochemical basis of
eukaryote signalling
processes. It is believed that certain odorant degrading enzymes
are required to
maintain the ongoing sensitivity of an insect’s olfactory
neuronal system by repriming
neurons. However, relatively few ODEs have been identified and
characterized to date,
especially in the model insect Drosophila melanogaster.
The study presented here takes biochemical, neurobiological and
behavioural
approaches to elucidate the role of ODEs in D. melanogaster.
After a review of relevant
literature in Chapter 1, Chapter 2 decodes the antennal
transcriptome of
D. melanogaster for the first time. Using high quality genome
sequence and
transcriptomic data for many other tissues of this species
already available, I identified
a few antennae-selective esterases, cytochrome P450s (P450s),
glutathione
S-transferases (GSTs) and UDP-glycosyltransferases (UGTs). Of
these, the activity of one
esterase JHEdup, against a range of volatile odorants was found
to be comparable with
other known ODEs from different species, mainly Lepidoptera. I
also identified the
presence of another esterase, EST6, at high levels in the
antennae. It has previously been
proposed that EST6 is a catalyst for the transformation of
pheromonal and kairomonal
esters to the corresponding alcohols and acids, thereby mediating
various mating
behaviours. I further examined the proposed effect of EST6 by
comparing wild type and
EST6 null flies at a neurobiological and behavioural level. The
findings, presented in
Chapter 3, show this enzyme is important for the flies to respond
to incoming volatile
odorants and affects their subsequent behaviours. Additionally,
EST6 has previously
been reported to hydrolyse cis-vaccenyl acetate (cVA), the major
pheromone known in
Drosophila, in vitro and recent electroantennogram (EAG)
experiments with EST6 wild
type and null flies exposed to cVA suggest that this might also
be an in vivo function. I
therefore conducted experiments to understand the biochemical
activity of EST6 against
cVA. I also measured its activity against 84 other bioactive
esters. The results
categorically show that EST6 has no activity against cVA but has
very good activity
against a wide range of fruit- and yeast-derived volatiles known
to play a role in
mediating female reproductive behaviour. These results are
presented in Chapter 4,
along with a crystal structure of EST6. The final chapter of this
thesis then discusses the overall findings of these studies and
offers a broader perspective on future directions. The three
major conclusions from the
work are as follows. Firstly, JHEdup and EST6 are broad range
ODEs active against a wide
range of food odorants. Secondly, EST6 may also have a role in
cVA processing but not
actually as an ODE against this substrate. Thirdly, ODEs may be a
fruitful system to
develop biocontrol systems for pest insects based on disrupting
their olfactory system.
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