World Congress of Malacology Antwerp ... - Unitas Malacologica
World Congress of Malacology Antwerp ... - Unitas Malacologica
World Congress of Malacology Antwerp ... - Unitas Malacologica
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adapted retinal mRNA showed 1.4- and 2-fold inductions <strong>of</strong> α-tubulin and S-crystallin, respectively,<br />
when compared to dark-adapted retinas. Percent volume analysis <strong>of</strong> dark-adapted retinal protein<br />
showed that α-tubulin and S-crystallin were 2-fold more abundant when compared to light-adapted<br />
retinas. Coinciding with the observed differential expression are the following morphological<br />
changes <strong>of</strong> dark- and light-adapted rhabdomeres: the number <strong>of</strong> rhabdomeric microvilli increase in<br />
the dark, resulting in the growth <strong>of</strong> rhabdomeres; whereas, there is a decrease in the number <strong>of</strong><br />
rhabdomeric microvilli in the light, resulting in the diminution <strong>of</strong> the rhabdomeres. We believe that<br />
mRNA for these cytoskeletal proteins may be stored and translated when needed in either the dark or<br />
light. If masking and unmasking <strong>of</strong> these mRNAs does occur, then regulatory elements or sequences<br />
should be present in the 3’UTR regions. CPEB is a 62 kDa trans-acting RNA binding protein, which<br />
binds to the variable CPE consensus sequence, U4-5A1-3U, in 3’ UTR regions <strong>of</strong> mRNA, and is<br />
indicated in temporal regulation <strong>of</strong> translational activation and repression. Using western blot<br />
analysis and immunocytochemistry, we have identified the presence <strong>of</strong> CPEB in dark- and lightadapted<br />
octopus retinas. Using 3’RACE analysis <strong>of</strong> the 3’ UTR regions <strong>of</strong> α-tubulin and S-crystallin<br />
mRNAs, we have detected the following CPE-like sequences in the 3’ UTR <strong>of</strong> isolated 326-bp Scrystallin<br />
A and B variants: UUUAACA, UUUUUAA, and UUUUA. The detection <strong>of</strong> CPEB and the<br />
identification <strong>of</strong> the putative CPE-like sequences in the S-crystallin 3’ UTR suggest that CPEB may<br />
be involved in the activation <strong>of</strong> masked S-crystallin mRNA, but not in the regulation <strong>of</strong> α-tubulin<br />
mRNA, resulting in increased S-crystallin protein synthesis in dark-adapted octopus retinas.<br />
Morphological and molecular characterization <strong>of</strong> the Roman snail Helix pomatia with data on<br />
the phylogeny <strong>of</strong> the genus Helix (Pulmonata, Helicidae)<br />
Ketmaier, Valerio 1 ; Fiorentino, Viviana 2 ; Tiedemann, Ralph 1 ; Manganelli, Giuseppe 2 ; Giusti,<br />
Folco 2<br />
1. Unit <strong>of</strong> Evolutionary Biology/Systematic Zoology, Institute <strong>of</strong> Biochemistry and Biology,<br />
University <strong>of</strong> Potsdam, Karl-Liebknecht-Str. 24-25, D-14476, Potsdam, Germany,<br />
Email: ketmaier@rz.uni-potsdam.de; tiedeman@rz.uni-potsdam.de<br />
2. Dipartimento di Scienze Ambientali “G. Sarfatti”, Università di Siena, Via Mattioli 4, I-53100,<br />
Siena, Italy,<br />
Email: vivianafiorentino@unisi.it; manganelli@unisi.it; giustif@unisi.it<br />
Diagnostic uncertainties have favoured fraudulent traffic <strong>of</strong> different edible snails which are sold<br />
under the name <strong>of</strong> the costly Roman snail: Helix pomatia. The application <strong>of</strong> molecular markers<br />
combined with diagnostic morphological characters is thus decisive for reliable identification <strong>of</strong> the<br />
species in natural and non-natural conditions as well as in prepared food products. Given the<br />
commercial value <strong>of</strong> the Roman snail and the lack <strong>of</strong> knowledge about its phylogeography, we<br />
endeavoured to cover most <strong>of</strong> the species range with our sampling (i.e. Sweden, Denmark, Germany,<br />
United Kingdom, France and Italy). The study is based on analysis <strong>of</strong> sequence variation at two<br />
mitochondrial (CO1 and 16S rRNA) and two nuclear (ITS-1 and ITS-2) genes plus detailed study <strong>of</strong><br />
genital structure. To place the study in a wider phylogenetic context we also included four congeneric<br />
species from European sites (H. campana, H. cincta, H. ligata and H. lucorum), plus four other<br />
helicids (Cornu aspersum, C. mazzullii, Eobania vermiculata and Helicigona lapicida) as outgroups.<br />
Molecular data supports the monophyly <strong>of</strong> the genus Helix and robustly clustered all Roman snail<br />
populations included in the study. We found seven haplotypes in H. pomatia, five <strong>of</strong> them unique to<br />
single populations and only two shared among different populations (France-NW Italy and Sweden-<br />
Denmark, respectively). The relatively little divergence detected among haplotypes (from 1 to 6<br />
substitutions) suggests recent northward expansion (historical and at least partly human-mediated) <strong>of</strong><br />
the species. The anatomical analyses are in full agreement with the above scenario. All <strong>of</strong> the Roman<br />
snail populations showed substantial uniformity <strong>of</strong> the genital characters examined.<br />
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