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Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination

The release of Ca(2+) from internal stores is a major source of signal Ca(2+) in almost all cell types. The internal Ca(2+) pools are activated via two main families of intracellular Ca(2+)-release channels, the ryanodine and the inositol 1,4,5-trisphosphate (InsP(3)) receptors. Among multicellular...

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Autores principales: Ladenburger, Eva-Maria, Plattner, Helmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213138/
https://www.ncbi.nlm.nih.gov/pubmed/22102876
http://dx.doi.org/10.1371/journal.pone.0027111
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author Ladenburger, Eva-Maria
Plattner, Helmut
author_facet Ladenburger, Eva-Maria
Plattner, Helmut
author_sort Ladenburger, Eva-Maria
collection PubMed
description The release of Ca(2+) from internal stores is a major source of signal Ca(2+) in almost all cell types. The internal Ca(2+) pools are activated via two main families of intracellular Ca(2+)-release channels, the ryanodine and the inositol 1,4,5-trisphosphate (InsP(3)) 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 InsP(3) and ryanodine receptors by BLAST search of the Paramecium database. We here report that these Ca(2+)-release channels may display all or only some of the characteristics of canonical InsP(3) 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 InsP(3) receptors, while a sequence homologous to the InsP(3)-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 Ca(2+) 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 InsP(3) 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.
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spelling pubmed-32131382011-11-18 Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination Ladenburger, Eva-Maria Plattner, Helmut PLoS One Research Article The release of Ca(2+) from internal stores is a major source of signal Ca(2+) in almost all cell types. The internal Ca(2+) pools are activated via two main families of intracellular Ca(2+)-release channels, the ryanodine and the inositol 1,4,5-trisphosphate (InsP(3)) 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 InsP(3) and ryanodine receptors by BLAST search of the Paramecium database. We here report that these Ca(2+)-release channels may display all or only some of the characteristics of canonical InsP(3) 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 InsP(3) receptors, while a sequence homologous to the InsP(3)-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 Ca(2+) 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 InsP(3) 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. Public Library of Science 2011-11-10 /pmc/articles/PMC3213138/ /pubmed/22102876 http://dx.doi.org/10.1371/journal.pone.0027111 Text en Ladenburger, Plattner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ladenburger, Eva-Maria
Plattner, Helmut
Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination
title Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination
title_full Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination
title_fullStr Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination
title_full_unstemmed Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination
title_short Calcium-Release Channels in Paramecium. Genomic Expansion, Differential Positioning and Partial Transcriptional Elimination
title_sort calcium-release channels in paramecium. genomic expansion, differential positioning and partial transcriptional elimination
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213138/
https://www.ncbi.nlm.nih.gov/pubmed/22102876
http://dx.doi.org/10.1371/journal.pone.0027111
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