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Calcium-release channels in paramecium : Genomic expansion, differential positioning and partial transcriptional elimination

Calcium-release channels in paramecium : Genomic expansion, differential positioning and partial transcriptional elimination

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LADENBURGER, Eva-Maria, Helmut PLATTNER, 2011. Calcium-release channels in paramecium : Genomic expansion, differential positioning and partial transcriptional elimination. In: PLoS ONE. 6(11), e27111. eISSN 1932-6203. Available under: doi: 10.1371/journal.pone.0027111

@article{Ladenburger2011Calci-18596, title={Calcium-release channels in paramecium : Genomic expansion, differential positioning and partial transcriptional elimination}, year={2011}, doi={10.1371/journal.pone.0027111}, number={11}, volume={6}, journal={PLoS ONE}, author={Ladenburger, Eva-Maria and Plattner, Helmut}, note={Article Number: e27111} }

<rdf:RDF xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:void="http://rdfs.org/ns/void#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/18596"> <dcterms:bibliographicCitation>First publ. in: PLoS ONE ; 6 (2011), 11. - e27111</dcterms:bibliographicCitation> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2012-03-02T08:13:41Z</dcterms:available> <foaf:homepage rdf:resource="http://localhost:8080/jspui"/> <dc:contributor>Plattner, Helmut</dc:contributor> <dc:rights>deposit-license</dc:rights> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2012-03-02T08:13:41Z</dc:date> <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/28"/> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/18596"/> <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/18596/1/ladenburger_plattner.pdf"/> <dc:contributor>Ladenburger, Eva-Maria</dc:contributor> <dc:creator>Plattner, Helmut</dc:creator> <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/> <dcterms:abstract xml:lang="eng">The release of Ca2+ from internal stores is a major source of signal Ca2+ in almost all cell types. The internal Ca2+ pools are activated via two main families of intracellular Ca2+-release channels, the ryanodine and the inositol 1,4,5-trisphosphate (InsP3) receptors. Among multicellular organisms these channel types are ubiquitous, whereas in most unicellular eukaryotes the identification of orthologs is impaired probably due to evolutionary sequence divergence. However, the ciliated protozoan Paramecium allowed us to prognosticate six groups, with a total of 34 genes, encoding proteins with characteristics typical of InsP3 and ryanodine receptors by BLAST search of the Paramecium database. We here report that these Ca2+-release channels may display all or only some of the characteristics of canonical InsP3 and ryanodine receptors. In all cases, prediction methods indicate the presence of six trans-membrane regions in the C-terminal domains, thus corresponding to canonical InsP3 receptors, while a sequence homologous to the InsP3-binding domain is present only in some types. Only two types have been analyzed in detail previously. We now show, by using antibodies and eventually by green fluorescent protein labeling, that the members of all six groups localize to distinct organelles known to participate in vesicle trafficking and, thus, may provide Ca2+ for local membrane-membrane interactions. Whole genome duplication can explain radiation within the six groups. Comparative and evolutionary evaluation suggests derivation from a common ancestor of canonical InsP3 and ryanodine receptors. With one group we could ascertain, to our knowledge for the first time, aberrant splicing in one thoroughly analyzed Paramecium gene. This yields truncated forms and, thus, may indicate a way to pseudogene formation. No comparable analysis is available for any other, free-living or parasitic/pathogenic protozoan.</dcterms:abstract> <dc:creator>Ladenburger, Eva-Maria</dc:creator> <dcterms:title>Calcium-release channels in paramecium : Genomic expansion, differential positioning and partial transcriptional elimination</dcterms:title> <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/rdf/resource/123456789/28"/> <dcterms:rights rdf:resource="http://nbn-resolving.org/urn:nbn:de:bsz:352-20140905103605204-4002607-1"/> <dc:language>eng</dc:language> <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/18596/1/ladenburger_plattner.pdf"/> <dcterms:issued>2011</dcterms:issued> </rdf:Description> </rdf:RDF>

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