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Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster

The foraging (for) gene of Drosophila melanogaster encodes a cGMP-dependent protein kinase (PKG), which is a major effector of the cGMP signaling pathway involved in the regulation of behaviour and metabolic traits. Despite being well studied at the transcript level, little is known about the for ge...

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Autores principales: Vasquez, Oscar E., Allen, Aaron M., So, Anthony K.-C., Nguyen, Quynh H., Krause, Henry M., Levine, Joel D., Sokolowski, Marla B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299703/
https://www.ncbi.nlm.nih.gov/pubmed/37373366
http://dx.doi.org/10.3390/ijms241210219
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author Vasquez, Oscar E.
Allen, Aaron M.
So, Anthony K.-C.
Nguyen, Quynh H.
Krause, Henry M.
Levine, Joel D.
Sokolowski, Marla B.
author_facet Vasquez, Oscar E.
Allen, Aaron M.
So, Anthony K.-C.
Nguyen, Quynh H.
Krause, Henry M.
Levine, Joel D.
Sokolowski, Marla B.
author_sort Vasquez, Oscar E.
collection PubMed
description The foraging (for) gene of Drosophila melanogaster encodes a cGMP-dependent protein kinase (PKG), which is a major effector of the cGMP signaling pathway involved in the regulation of behaviour and metabolic traits. Despite being well studied at the transcript level, little is known about the for gene at the protein level. Here, we provide a detailed characterization of the for gene protein (FOR) products and present new tools for their study, including five isoform-specific antibodies and a transgenic strain that carries an HA-labelled for allele (for(BAC)::HA). Our results showed that multiple FOR isoforms were expressed in the larval and adult stages of D. melanogaster and that the majority of whole-body FOR expression arises from three (P1, P1α, and P3) of eight putative protein isoforms. We found that FOR expression differed between the larval and adult stages and between the dissected larval organs we analyzed, which included the central nervous system (CNS), fat body, carcass, and intestine. Moreover, we showed that the FOR expression differed between two allelic variants of the for gene, namely, for(s) (sitter) and for(R) (rover), that are known to differ in many food-related traits. Together, our in vivo identification of FOR isoforms and the existence of temporal, spatial, and genetic differences in their expression lay the groundwork for determining their functional significance.
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spelling pubmed-102997032023-06-28 Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster Vasquez, Oscar E. Allen, Aaron M. So, Anthony K.-C. Nguyen, Quynh H. Krause, Henry M. Levine, Joel D. Sokolowski, Marla B. Int J Mol Sci Article The foraging (for) gene of Drosophila melanogaster encodes a cGMP-dependent protein kinase (PKG), which is a major effector of the cGMP signaling pathway involved in the regulation of behaviour and metabolic traits. Despite being well studied at the transcript level, little is known about the for gene at the protein level. Here, we provide a detailed characterization of the for gene protein (FOR) products and present new tools for their study, including five isoform-specific antibodies and a transgenic strain that carries an HA-labelled for allele (for(BAC)::HA). Our results showed that multiple FOR isoforms were expressed in the larval and adult stages of D. melanogaster and that the majority of whole-body FOR expression arises from three (P1, P1α, and P3) of eight putative protein isoforms. We found that FOR expression differed between the larval and adult stages and between the dissected larval organs we analyzed, which included the central nervous system (CNS), fat body, carcass, and intestine. Moreover, we showed that the FOR expression differed between two allelic variants of the for gene, namely, for(s) (sitter) and for(R) (rover), that are known to differ in many food-related traits. Together, our in vivo identification of FOR isoforms and the existence of temporal, spatial, and genetic differences in their expression lay the groundwork for determining their functional significance. MDPI 2023-06-16 /pmc/articles/PMC10299703/ /pubmed/37373366 http://dx.doi.org/10.3390/ijms241210219 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vasquez, Oscar E.
Allen, Aaron M.
So, Anthony K.-C.
Nguyen, Quynh H.
Krause, Henry M.
Levine, Joel D.
Sokolowski, Marla B.
Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster
title Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster
title_full Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster
title_fullStr Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster
title_full_unstemmed Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster
title_short Characterizing the Protein Isoforms of foraging (for), the PKGI Ortholog in Drosophila melanogaster
title_sort characterizing the protein isoforms of foraging (for), the pkgi ortholog in drosophila melanogaster
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299703/
https://www.ncbi.nlm.nih.gov/pubmed/37373366
http://dx.doi.org/10.3390/ijms241210219
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