The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system

dc.contributor.authorPlattner, Helmut
dc.contributor.authorVerkhratsky, Alexei
dc.date.accessioned2018-04-16T07:28:40Z
dc.date.available2018-04-16T07:28:40Z
dc.date.issued2018-07eng
dc.description.abstractThe aim of the present article is to analyse the evolutionary links between protozoa and neuronal and neurosecretory cells. To this effect we employ functional and topological data available for ciliates, in particular for Paramecium. Of note, much less data are available for choanoflagellates, the progenitors of metazoans, which currently are in the focus of metazoan genomic data mining. Key molecular players are found from the base to the highest levels of eukaryote evolution, including neurones and neurosecretory cells. Several common fundamental mechanisms, such as SNARE proteins and assembly of exocytosis sites, GTPases, Ca2+-sensors, voltage-gated Ca2+-influx channels and their inhibition by the forming Ca2+/calmodulin complex are conserved, albeit with different subcellular channel localisation, from protozoans to man. Similarly, Ca2+-release channels represented by InsP3 receptors and putative precursors of ryanodine receptors, which all emerged in protozoa, serve for focal intracellular Ca2+ signalling from ciliates to mammalian neuronal cells, eventually in conjunction with store-operated Ca2+-influx. Restriction of Ca2+ signals by high capacity/low affinity Ca2+-binding proteins is maintained throughout the evolutionary tree although the proteins involved differ between the taxa. Phosphatase 2B/calcineurin appears to be involved in signalling and in membrane recycling throughout evolution. Most impressive example of evolutionary conservation is the sub-second dynamics of exocytosis-endocytosis coupling in Paramecium cells, with similar kinetics in neuronal and neurosecretory systems. Numerous cell surface receptors and channels that emerge in protozoa operate in the human nervous system, whereas a variety of cell adhesion molecules are newly “invented” during evolution, enabled by an increase in gene numbers, alternative splice forms and transcription factors. Thereby, important regulatory and signalling molecules are retained as a protozoan heritage.eng
dc.description.versionpublishedde
dc.identifier.doi10.1016/j.ceca.2018.04.001eng
dc.identifier.ppn502056665
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/42031
dc.language.isoengeng
dc.rightsterms-of-use
dc.rights.urihttps://rightsstatements.org/page/InC/1.0/
dc.subjectBrain; Ca2+; Calcium; Ciliate; Evolution; Neurone; Neurosecretory; Protozoa; Signallingeng
dc.subject.ddc570eng
dc.titleThe remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous systemeng
dc.typeJOURNAL_ARTICLEde
dspace.entity.typePublication
kops.citation.bibtex
@article{Plattner2018-07remem-42031,
  year={2018},
  doi={10.1016/j.ceca.2018.04.001},
  title={The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system},
  volume={73},
  issn={0143-4160},
  journal={Cell Calcium},
  pages={25--39},
  author={Plattner, Helmut and Verkhratsky, Alexei}
}
kops.citation.iso690PLATTNER, Helmut, Alexei VERKHRATSKY, 2018. The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system. In: Cell Calcium. 2018, 73, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001deu
kops.citation.iso690PLATTNER, Helmut, Alexei VERKHRATSKY, 2018. The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system. In: Cell Calcium. 2018, 73, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001eng
kops.citation.rdf
<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/server/rdf/resource/123456789/42031">
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dc:creator>Plattner, Helmut</dc:creator>
    <dcterms:title>The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system</dcterms:title>
    <dc:language>eng</dc:language>
    <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2018-04-16T07:28:40Z</dc:date>
    <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/42031/1/Plattner_2-820qa8shx6mx4.pdf"/>
    <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/42031"/>
    <dc:contributor>Verkhratsky, Alexei</dc:contributor>
    <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/42031/1/Plattner_2-820qa8shx6mx4.pdf"/>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dcterms:issued>2018-07</dcterms:issued>
    <dc:contributor>Plattner, Helmut</dc:contributor>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dc:creator>Verkhratsky, Alexei</dc:creator>
    <dc:rights>terms-of-use</dc:rights>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2018-04-16T07:28:40Z</dcterms:available>
    <dcterms:abstract xml:lang="eng">The aim of the present article is to analyse the evolutionary links between protozoa and neuronal and neurosecretory cells. To this effect we employ functional and topological data available for ciliates, in particular for Paramecium. Of note, much less data are available for choanoflagellates, the progenitors of metazoans, which currently are in the focus of metazoan genomic data mining. Key molecular players are found from the base to the highest levels of eukaryote evolution, including neurones and neurosecretory cells. Several common fundamental mechanisms, such as SNARE proteins and assembly of exocytosis sites, GTPases, Ca&lt;sup&gt;2+&lt;/sup&gt;-sensors, voltage-gated Ca&lt;sup&gt;2+&lt;/sup&gt;-influx channels and their inhibition by the forming Ca&lt;sup&gt;2+&lt;/sup&gt;/calmodulin complex are conserved, albeit with different subcellular channel localisation, from protozoans to man. Similarly, Ca&lt;sup&gt;2+&lt;/sup&gt;-release channels represented by InsP3 receptors and putative precursors of ryanodine receptors, which all emerged in protozoa, serve for focal intracellular Ca&lt;sup&gt;2+&lt;/sup&gt; signalling from ciliates to mammalian neuronal cells, eventually in conjunction with store-operated Ca&lt;sup&gt;2+&lt;/sup&gt;-influx. Restriction of Ca&lt;sup&gt;2+&lt;/sup&gt; signals by high capacity/low affinity Ca&lt;sup&gt;2+&lt;/sup&gt;-binding proteins is maintained throughout the evolutionary tree although the proteins involved differ between the taxa. Phosphatase 2B/calcineurin appears to be involved in signalling and in membrane recycling throughout evolution. Most impressive example of evolutionary conservation is the sub-second dynamics of exocytosis-endocytosis coupling in Paramecium cells, with similar kinetics in neuronal and neurosecretory systems. Numerous cell surface receptors and channels that emerge in protozoa operate in the human nervous system, whereas a variety of cell adhesion molecules are newly “invented” during evolution, enabled by an increase in gene numbers, alternative splice forms and transcription factors. Thereby, important regulatory and signalling molecules are retained as a protozoan heritage.</dcterms:abstract>
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
  </rdf:Description>
</rdf:RDF>
kops.description.openAccessopenaccessgreen
kops.flag.isPeerReviewedtrue
kops.identifier.nbnurn:nbn:de:bsz:352-2-820qa8shx6mx4
kops.sourcefieldCell Calcium. 2018, <b>73</b>, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001deu
kops.sourcefield.plainCell Calcium. 2018, 73, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001deu
kops.sourcefield.plainCell Calcium. 2018, 73, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001eng
relation.isAuthorOfPublicationf99b668b-482b-49ec-8891-bc63a63a9ebb
relation.isAuthorOfPublication.latestForDiscoveryf99b668b-482b-49ec-8891-bc63a63a9ebb
source.bibliographicInfo.fromPage25eng
source.bibliographicInfo.toPage39eng
source.bibliographicInfo.volume73eng
source.identifier.eissn1532-1991eng
source.identifier.issn0143-4160eng
source.periodicalTitleCell Calciumeng

Dateien

Originalbündel

Gerade angezeigt 1 - 1 von 1
Vorschaubild nicht verfügbar
Name:
Plattner_2-820qa8shx6mx4.pdf
Größe:
738 KB
Format:
Adobe Portable Document Format
Beschreibung:
Plattner_2-820qa8shx6mx4.pdf
Plattner_2-820qa8shx6mx4.pdfGröße: 738 KBDownloads: 876