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      Ancestral glycoprotein hormone-receptor pathway controls growth in C. elegans

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          Abstract

          In vertebrates, thyrostimulin is a highly conserved glycoprotein hormone that, besides thyroid stimulating hormone (TSH), is a potent ligand of the TSH receptor. Thyrostimulin is considered the most ancestral glycoprotein hormone and orthologs of its subunits, GPA2 and GPB5, are widely conserved across vertebrate and invertebrate animals. Unlike TSH, however, the functions of the thyrostimulin neuroendocrine system remain largely unexplored. Here, we identify a functional thyrostimulin-like signaling system in Caenorhabditis elegans. We show that orthologs of GPA2 and GPB5, together with thyrotropin-releasing hormone (TRH) related neuropeptides, constitute a neuroendocrine pathway that promotes growth in C. elegans. GPA2/GPB5 signaling is required for normal body size and acts through activation of the glycoprotein hormone receptor ortholog FSHR-1. C. elegans GPA2 and GPB5 increase cAMP signaling by FSHR-1 in vitro. Both subunits are expressed in enteric neurons and promote growth by signaling to their receptor in glial cells and the intestine. Impaired GPA2/GPB5 signaling causes bloating of the intestinal lumen. In addition, mutants lacking thyrostimulin-like signaling show an increased defecation cycle period. Our study suggests that the thyrostimulin GPA2/GPB5 pathway is an ancient enteric neuroendocrine system that regulates intestinal function in ecdysozoans, and may ancestrally have been involved in the control of organismal growth.

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          Molecular topography of an entire nervous system

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            Global view of the evolution and diversity of metazoan neuropeptide signaling.

            Neuropeptides are signaling molecules that commonly act via G protein-coupled receptors (GPCRs) and are generated in neurons by proneuropeptide (pNP) cleavage. Present in both cnidarians and bilaterians, neuropeptides represent an ancient and widespread mode of neuronal communication. Due to the inherent difficulties of analyzing highly diverse and repetitive pNPs, the relationships among different families are often elusive. Using similarity-based clustering and sensitive similarity searches, I obtained a global view of metazoan pNP diversity and evolution. Clustering revealed a large and diffuse network of sequences connected by significant sequence similarity encompassing one-quarter of all families. pNPs belonging to this cluster were also identified in the early-branching neuronless animal Trichoplax adhaerens. Clustering of neuropeptide GPCRs identified several orthology groups and allowed the reconstruction of the phyletic distribution of receptor families. GPCR phyletic distribution closely paralleled that of pNPs, indicating extensive conservation and long-term coevolution of receptor-ligand pairs. Receptor orthology and intermediate sequences also revealed the homology of pNPs so far considered unrelated, including allatotropin and orexin. These findings, together with the identification of deuterostome achatin and luqin and protostome opioid pNPs, extended the neuropeptide complement of the urbilaterian. Several pNPs were also identified from the hemichordate Saccoglossus kowalevskii and the cephalochordate Branchiostoma floridae, elucidating pNP evolution in deuterostomes. Receptor-ligand conservation also allowed ligand predictions for many uncharacterized GPCRs from nonmodel species. The reconstruction of the neuropeptide-signaling repertoire at deep nodes of the animal phylogeny allowed the formulation of a testable scenario of the evolution of animal neuroendocrine systems.
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              Robust Genome Editing with Short Single-Stranded and Long, Partially Single-Stranded DNA Donors in Caenorhabditis elegans

              A robust genome editing pipeline is critical to the vitality of a modern genetic laboratory. Previous studies have shown that Cas9 ribonucleoprotein (RNP)-based editing can be highly effective in Caenorhabditis elegans, particularly...
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                Author and article information

                Contributors
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                20 June 2023
                2023
                : 14
                : 1200407
                Affiliations
                [1] 1 Neural Signaling and Circuit Plasticity Group, Department of Biology , KU Leuven, Leuven, Belgium
                [2] 2 Functional Genomics and Proteomics Group, Department of Biology , KU Leuven, Leuven, Belgium
                Author notes

                Edited by: James A. Carr, Texas Tech University, United States

                Reviewed by: Carlos Diaz-Balzac, University of Rochester, United States; Jean-Paul V. Paluzzi, York University, Canada

                *Correspondence: Isabel Beets, isabel.beets@ 123456kuleuven.be
                Article
                10.3389/fendo.2023.1200407
                10319355
                37409228
                adbc691e-eec5-46c7-a34f-a66d22cb1695
                Copyright © 2023 Kenis, Istiban, Van Damme, Vandewyer, Watteyne, Schoofs and Beets

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 04 April 2023
                : 23 May 2023
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 109, Pages: 15, Words: 7967
                Funding
                This research was supported by the Research Foundation Flanders (FWO) grant G0C0618N and KU Leuven Research Council grant C16/19/003 (to IB and LS). SD is a fellow of the Research Foundation Flanders (FWO) and JW is supported by a postdoctoral fellowship of the KU Leuven Research Council.
                Categories
                Endocrinology
                Original Research
                Custom metadata
                Neuroendocrine Science

                Endocrinology & Diabetes
                glycoprotein hormone,thyrostimulin,g protein-coupled receptor,growth regulation,c. elegans

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