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Drosophila molting neurohormone bursicon is a heterodimer and the natural agonist of the orphan receptor DLGR2
Authors:Mendive Fernando M  Van Loy Tom  Claeysen Sylvie  Poels Jeroen  Williamson Michael  Hauser Frank  Grimmelikhuijzen Cornelis J P  Vassart Gilbert  Vanden Broeck Jozef
Affiliation:Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (IRIBHM), Université Libre de Bruxelles, Campus Erasme, 808 Route de Lennik, B-1070 Bruxelles, Belgium.
Abstract:Bursicon is a neurohumoral agent responsible for tanning and hardening of the cuticle and expansion of the wings during the final phase of insect metamorphosis. Although the hormonal activity was described more than 40 years ago, the molecular nature of bursicon has remained elusive. We identify here Drosophila bioactive bursicon as a heterodimer made of two cystine knot polypeptides. This conclusion was reached in part from the unexpected observation that in the genome of the honey bee, the orthologs of the two Drosophila proteins are predicted to be fused in a single open reading frame. The heterodimeric Drosophila protein displays bursicon bioactivity in freshly enclosed neck-ligated flies and is the natural agonist of the orphan G protein-coupled receptor DLGR2.
Keywords:ORF, open reading frame   LGR, leucine-rich repeats containing G protein-coupled receptor   CTCK, C-terminal cystine knot   WGS, whole-genome sequencing   Bursα, bursicon α subunit   Bursβ, bursicon β subunit
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