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A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning

Insect Gustatory and Odorant Receptors (GRs and ORs) form a superfamily of novel transmembrane proteins, which are expressed in chemosensory neurons that detect environmental stimuli. Here we identify homologues of GRs (Gustatory receptor-like (Grl) genes) in genomes across Protostomia, Deuterostomi...

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Autores principales: Saina, Michael, Busengdal, Henriette, Sinigaglia, Chiara, Petrone, Libero, Oliveri, Paola, Rentzsch, Fabian, Benton, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374167/
https://www.ncbi.nlm.nih.gov/pubmed/25692633
http://dx.doi.org/10.1038/ncomms7243
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author Saina, Michael
Busengdal, Henriette
Sinigaglia, Chiara
Petrone, Libero
Oliveri, Paola
Rentzsch, Fabian
Benton, Richard
author_facet Saina, Michael
Busengdal, Henriette
Sinigaglia, Chiara
Petrone, Libero
Oliveri, Paola
Rentzsch, Fabian
Benton, Richard
author_sort Saina, Michael
collection PubMed
description Insect Gustatory and Odorant Receptors (GRs and ORs) form a superfamily of novel transmembrane proteins, which are expressed in chemosensory neurons that detect environmental stimuli. Here we identify homologues of GRs (Gustatory receptor-like (Grl) genes) in genomes across Protostomia, Deuterostomia and non-Bilateria. Surprisingly, two Grls in the cnidarian Nematostella vectensis, NvecGrl1 and NvecGrl2, are expressed early in development, in the blastula and gastrula, but not at later stages when a putative chemosensory organ forms. NvecGrl1 transcripts are detected around the arboral pole, considered the equivalent to the head-forming region of Bilateria. Morpholino-mediated knockdown of NvecGrl1 causes developmental patterning defects of this region, leading to animals lacking the apical sensory organ. A deuterostome Grl from the sea urchin Strongylocentrotus purpuratus displays similar patterns of developmental expression. These results reveal an early evolutionary origin of the insect chemosensory receptor family, and raise the possibility that their ancestral role was in embryonic development.
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spelling pubmed-43741672015-08-18 A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning Saina, Michael Busengdal, Henriette Sinigaglia, Chiara Petrone, Libero Oliveri, Paola Rentzsch, Fabian Benton, Richard Nat Commun Article Insect Gustatory and Odorant Receptors (GRs and ORs) form a superfamily of novel transmembrane proteins, which are expressed in chemosensory neurons that detect environmental stimuli. Here we identify homologues of GRs (Gustatory receptor-like (Grl) genes) in genomes across Protostomia, Deuterostomia and non-Bilateria. Surprisingly, two Grls in the cnidarian Nematostella vectensis, NvecGrl1 and NvecGrl2, are expressed early in development, in the blastula and gastrula, but not at later stages when a putative chemosensory organ forms. NvecGrl1 transcripts are detected around the arboral pole, considered the equivalent to the head-forming region of Bilateria. Morpholino-mediated knockdown of NvecGrl1 causes developmental patterning defects of this region, leading to animals lacking the apical sensory organ. A deuterostome Grl from the sea urchin Strongylocentrotus purpuratus displays similar patterns of developmental expression. These results reveal an early evolutionary origin of the insect chemosensory receptor family, and raise the possibility that their ancestral role was in embryonic development. 2015-02-18 /pmc/articles/PMC4374167/ /pubmed/25692633 http://dx.doi.org/10.1038/ncomms7243 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Saina, Michael
Busengdal, Henriette
Sinigaglia, Chiara
Petrone, Libero
Oliveri, Paola
Rentzsch, Fabian
Benton, Richard
A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
title A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
title_full A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
title_fullStr A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
title_full_unstemmed A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
title_short A cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
title_sort cnidarian homologue of an insect gustatory receptor functions in developmental body patterning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374167/
https://www.ncbi.nlm.nih.gov/pubmed/25692633
http://dx.doi.org/10.1038/ncomms7243
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