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

Author:

Vasquez Oscar E.1,Allen Aaron M.2ORCID,So Anthony K.-C.3,Nguyen Quynh H.4,Krause Henry M.5ORCID,Levine Joel D.36,Sokolowski Marla B.16

Affiliation:

1. Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, ON M5S 3B2, Canada

2. Centre for Neural Circuits and Behaviour, Oxford University, Oxford OX1 3SR, UK

3. Department of Biology, University of Toronto at Mississauga, Mississauga, ON L5L 1C6, Canada

4. Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada

5. Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 3E1, Canada

6. Child and Brain Development Program, Canadian Institute for Advanced Research (CIFAR), Toronto, ON M5G 1M1, Canada

Abstract

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 (forBAC::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, fors (sitter) and forR (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.

Funder

Natural Sciences and Engineering Council of Canada

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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