The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system
| dc.contributor.author | Plattner, Helmut | |
| dc.contributor.author | Verkhratsky, Alexei | |
| dc.date.accessioned | 2018-04-16T07:28:40Z | |
| dc.date.available | 2018-04-16T07:28:40Z | |
| dc.date.issued | 2018-07 | eng |
| dc.description.abstract | 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, 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.version | published | de |
| dc.identifier.doi | 10.1016/j.ceca.2018.04.001 | eng |
| dc.identifier.ppn | 502056665 | |
| dc.identifier.uri | https://kops.uni-konstanz.de/handle/123456789/42031 | |
| dc.language.iso | eng | eng |
| dc.rights | terms-of-use | |
| dc.rights.uri | https://rightsstatements.org/page/InC/1.0/ | |
| dc.subject | Brain; Ca2+; Calcium; Ciliate; Evolution; Neurone; Neurosecretory; Protozoa; Signalling | eng |
| dc.subject.ddc | 570 | eng |
| dc.title | The remembrance of the things past : Conserved signalling pathways link protozoa to mammalian nervous system | eng |
| dc.type | JOURNAL_ARTICLE | de |
| dspace.entity.type | Publication | |
| 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.iso690 | PLATTNER, 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.2018.04.001 | deu |
| kops.citation.iso690 | PLATTNER, 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.2018.04.001 | eng |
| 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<sup>2+</sup>-sensors, voltage-gated Ca<sup>2+</sup>-influx channels and their inhibition by the forming Ca<sup>2+</sup>/calmodulin complex are conserved, albeit with different subcellular channel localisation, from protozoans to man. Similarly, Ca<sup>2+</sup>-release channels represented by InsP3 receptors and putative precursors of ryanodine receptors, which all emerged in protozoa, serve for focal intracellular Ca<sup>2+</sup> signalling from ciliates to mammalian neuronal cells, eventually in conjunction with store-operated Ca<sup>2+</sup>-influx. Restriction of Ca<sup>2+</sup> signals by high capacity/low affinity Ca<sup>2+</sup>-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.openAccess | openaccessgreen | |
| kops.flag.isPeerReviewed | true | |
| kops.identifier.nbn | urn:nbn:de:bsz:352-2-820qa8shx6mx4 | |
| kops.sourcefield | Cell Calcium. 2018, <b>73</b>, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001 | deu |
| kops.sourcefield.plain | Cell Calcium. 2018, 73, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001 | deu |
| kops.sourcefield.plain | Cell Calcium. 2018, 73, pp. 25-39. ISSN 0143-4160. eISSN 1532-1991. Available under: doi: 10.1016/j.ceca.2018.04.001 | eng |
| relation.isAuthorOfPublication | f99b668b-482b-49ec-8891-bc63a63a9ebb | |
| relation.isAuthorOfPublication.latestForDiscovery | f99b668b-482b-49ec-8891-bc63a63a9ebb | |
| source.bibliographicInfo.fromPage | 25 | eng |
| source.bibliographicInfo.toPage | 39 | eng |
| source.bibliographicInfo.volume | 73 | eng |
| source.identifier.eissn | 1532-1991 | eng |
| source.identifier.issn | 0143-4160 | eng |
| source.periodicalTitle | Cell Calcium | eng |
Dateien
Originalbündel
1 - 1 von 1
Vorschaubild nicht verfügbar
- Name:
- Plattner_2-820qa8shx6mx4.pdf
- Größe:
- 738 KB
- Format:
- Adobe Portable Document Format
- Beschreibung:
