38
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      The Neuropeptide Corazonin Controls Social Behavior and Caste Identity in Ants

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          <p id="P1">Social insects are emerging models to study how gene regulation affects behavior because their colonies comprise individuals with the same genomes but greatly different behavioral repertoires. To investigate the molecular mechanisms that activate distinct behaviors in different castes, we exploited a natural behavioral plasticity in <i>Harpegnathos saltator</i>, where adult workers can transition to a reproductive, queen-like state called gamergate. Analysis of brain transcriptomes during the transition revealed that corazonin, a neuropeptide homologous to the vertebrate gonadotropin-releasing hormone, was downregulated as workers became gamergates. Corazonin was also preferentially expressed in workers and/or foragers from other social insect species. Injection of corazonin in transitioning <i>Harpegnathos</i> individuals suppressed expression of vitellogenin in the brain and stimulated worker-like hunting behaviors, while inhibiting gamergate behaviors such as dueling and egg deposition. We propose that corazonin is a central regulator of caste identity and behavior in social insects. </p><p id="P2">Corazonin controls behavioral transitions between ant workers and pseudo-queens.</p><p id="P3"> <div class="figure-container so-text-align-c"> <img alt="" class="figure" src="/document_file/095e699e-c606-4e4a-91ce-55e7fab77827/PubMedCentral/image/nihms893672u1.jpg"/> </div> </p>

          Related collections

          Most cited references53

          • Record: found
          • Abstract: found
          • Article: not found

          Using FlyAtlas to identify better Drosophila melanogaster models of human disease.

          FlyAtlas, a new online resource, provides the most comprehensive view yet of expression in multiple tissues of Drosophila melanogaster. Meta-analysis of the data shows that a significant fraction of the genome is expressed with great tissue specificity in the adult, demonstrating the need for the functional genomic community to embrace a wide range of functional phenotypes. Well-known developmental genes are often reused in surprising tissues in the adult, suggesting new functions. The homologs of many human genetic disease loci show selective expression in the Drosophila tissues analogous to the affected human tissues, providing a useful filter for potential candidate genes. Additionally, the contributions of each tissue to the whole-fly array signal can be calculated, demonstrating the limitations of whole-organism approaches to functional genomics and allowing modeling of a simple tissue fractionation procedure that should improve detection of weak or tissue-specific signals.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Genes and social behavior.

            What genes and regulatory sequences contribute to the organization and functioning of neural circuits and molecular pathways in the brain that support social behavior? How does social experience interact with information in the genome to modulate brain activity? Here, we address these questions by highlighting progress that has been made in identifying and understanding two key "vectors of influence" that link genes, the brain, and social behavior: (i) Social information alters gene expression in the brain to influence behavior, and (ii) genetic variation influences brain function and social behavior. We also discuss how evolutionary changes in genomic elements influence social behavior and outline prospects for a systems biology of social behavior.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              A fructose receptor functions as a nutrient sensor in the Drosophila brain.

              Internal nutrient sensors play important roles in feeding behavior, yet their molecular structure and mechanism of action are poorly understood. Using Ca(2+) imaging and behavioral assays, we show that the gustatory receptor 43a (Gr43a) functions as a narrowly tuned fructose receptor in taste neurons. Remarkably, Gr43a also functions as a fructose receptor in the brain. Interestingly, hemolymph fructose levels are tightly linked to feeding status: after nutritious carbohydrate consumption, fructose levels rise several fold and reach a concentration sufficient to activate Gr43a in the brain. By using different feeding paradigms and artificial activation of Gr43a-expressing brain neurons, we show that Gr43a is both necessary and sufficient to sense hemolymph fructose and promote feeding in hungry flies but suppress feeding in satiated flies. Thus, our studies indicate that the Gr43a-expressing brain neurons function as a nutrient sensor for hemolymph fructose and assign opposing valence to feeding experiences in a satiation-dependent manner. Copyright © 2012 Elsevier Inc. All rights reserved.
                Bookmark

                Author and article information

                Journal
                Cell
                Cell
                Elsevier BV
                00928674
                August 2017
                August 2017
                : 170
                : 4
                : 748-759.e12
                Article
                10.1016/j.cell.2017.07.014
                5564227
                28802044
                300ff67b-b586-4c99-9b85-8e2754582b8c
                © 2017
                History

                Comments

                Comment on this article