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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

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