Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
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#P66 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
Integrating heterogeneous Odor Response Data into a<br />
common Response Model: A DoOR to the Complete<br />
Olfactome<br />
C Giovanni Galizia 1 , Daniel Munch 1 , Martin Strauch 1 ,<br />
Anja Nissler 2 , Shouwen Ma 1<br />
1<br />
Universitat Konstanz Konstanz, Germany, 2 Humboldt<br />
Universität Berlin, Germany<br />
We have developed a new computational framework <strong>for</strong> merging<br />
odor response datasets from heterogeneous studies, creating a<br />
consensus meta-database, the Database of Odor Responses<br />
(DoOR). As a result we obtained a functional atlas of all available<br />
odor responses in Drosophila melanogaster. Both the program and<br />
the dataset are freely accessible and downloadable on the Internet<br />
(http://neuro.uni-konstanz.de/DoOR). The procedure can be<br />
adapted to other species, thus creating a family of “olfactomes” in<br />
the near future. D. melanogaster was chosen because of all species<br />
in this one we are closest to the complete olfactome, with the<br />
highest number of deorphanized receptors available. The database<br />
guarantees long-term stability (by offering time-stamped,<br />
downloadable versions), up-to-date accuracy (by including new<br />
datasets as soon as they are published), and portability (<strong>for</strong> other<br />
species). We hope that this comprehensive repository of odor<br />
response profiles will be useful to the olfactory community and to<br />
computational neuroscientists alike. Acknowledgements: BMBF<br />
grant 576/07 to MS and CGG, and DFG grant GA524/7-1 to<br />
DM. MS is an associated member of the DFG research training<br />
group GK-1042<br />
#P68 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
Splice variants of the Ca 2+ -activated Cl - channel Anoctamin 2<br />
Samsudeen Ponissery Saidu 1 , Aaron B. Stephan 2 , Sonia M.<br />
Caraballo 2 , Haiqing Zhao 2 , Johannes Reisert 1<br />
1<br />
Monell Chemical Senses Center Philadelphia, PA, USA,<br />
2<br />
Department of Biology, The Johns Hopkins University<br />
Baltimore, MD, USA<br />
Olfactory receptor neurons (ORNs) in vertebrates use a calciumactivated<br />
chloride current to amplify the receptor potential in<br />
response to odor stimulation. Anoctamin 2 (ANO2, also called<br />
TMEM16B) has recently been proposed to be the long-sought<br />
calcium-activated chloride channel in the ORN (Stephan et al,<br />
2009). Biophysical properties of heterologously-expressed ANO2<br />
channels are similar to those of the native calcium-activated<br />
channel, but with one noticeable difference: the native channel<br />
inactivates during prolonged opening at positive membrane<br />
potentials, whereas the heterologously expressed ANO2 channel<br />
does not. Different splice variants of ANO2 transcripts have been<br />
found in tissues including the olfactory epithelium and the retina.<br />
Using molecular techniques we found two alternative, hitherto<br />
not described ANO2 transcripts in ORNs, with alternative<br />
transcription initiation sites. Expression in a heterologous system<br />
and excised patch recordings yielded functional channels with<br />
biophysical properties largely similar to previously described<br />
ANO2 splice variants. To better understand the functional<br />
significance of various splice variants, we will further investigate<br />
biophysical properties of splice variants. Acknowledgements: This<br />
work is supported by a Morley Kare Fellowship, the Human<br />
Frontiers Science Organization and NIH R01 DC007395.<br />
P O S T E R S<br />
#P67 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
The multiple PDZ domain protein 1 (MUPP1) – mediator of<br />
the olfactosome?<br />
Sabrina Baumgart 1 , Robert Menzler 1 , Ruth Dooley 2 , Hanns Hatt 1 ,<br />
Eva Maria Neuhaus 3<br />
1<br />
1 Bochum, Germany, 2 Dublin, Ireland, 3 Berlin, Germany<br />
The complex olfactory signal transduction pathway enables<br />
mammals to detect and discriminate between thousands of<br />
different odorants. But how the individual components of this<br />
complex signaling cascade get into close proximity to each other is<br />
an unsolved question. We recently showed that a PDZ protein<br />
called MUPP1 (multiple PDZ domain protein 1) is an interaction<br />
partner of olfactory receptors and thereby a putative mediator of a<br />
so called olfactosome (Baumgart et al, FEBS journal, Dec 2009).<br />
This scaffolding protein consists of 13 single PDZ domains and is<br />
known to be a mediator of diverse GPCR based signalling<br />
networks. We demonstrated that this scaffolding protein is highly<br />
expressed in the dendritic knobs and cilia of olfactory sensory<br />
neurons of mice. Further, we could show that different ORs are<br />
able to interact with MUPP1. In a new peptide microarray<br />
approach we investigate putative interactions of a great variety of<br />
ORs of all different known subfamilies in the mouse genome. In<br />
addition, we investigate other signaling components <strong>for</strong> their<br />
putative presence in the MUPP1 based complex by protein<br />
microarrays, as well as by direct protein-protein interaction<br />
assays.<br />
<strong>Abstracts</strong> are printed as submitted by the author(s)<br />
#P69 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
An electroolfactogram (EOG) study of odor response maps<br />
from the mouse olfactory mucosa?<br />
David M Coppola 1 , Sarah M Held 1 , David A Brooks 1 ,<br />
Chris T Waggener 2<br />
1<br />
Department of Biology, Randolph Macon College Ashland, VA,<br />
USA, 2 Department of Biology, Virginia Commonwealth<br />
University Richmond, VA, USA<br />
Olfactory sensory neuron (OSN) responses measured at the<br />
population level tend to be spatially heterogeneous in vertebrates<br />
and response “maps” vary with odor. One proximate explanation<br />
<strong>for</strong> this heterogeneity comes from evidence that olfactory receptor<br />
genes in rodents are expressed in OSN populations that are<br />
spatially restricted to one of four zones in the nasal cavity. An<br />
ultimate explanation <strong>for</strong> response anisotropy posits that it is the<br />
signature of a supplementary mechanism <strong>for</strong> quality coding, based<br />
on the sorptive properties of odor molecules. These theories are<br />
difficult to assess because most mapping studies have utilized few<br />
odors, have provided little replication, or have involved but a<br />
single species (rat). In fact, to our knowledge, a detailed olfactory<br />
response map has not been reported <strong>for</strong> mouse, the species in<br />
which most of the gene localization work has been done. Here we<br />
report the results of a study of the mouse olfactory mucosal<br />
response map using the EOG. We focused on the medial aspect of<br />
olfactory turbinates as viewed in midsagittal section. This limited<br />
<strong>Abstracts</strong> | 49