Intron retention of an adhesion GPCR generates single transmembrane-helix isoforms to enable 7TM-adhesion GPCR function

Abstract

SUMMARYAdhesion G protein-coupled receptors (aGPCR) function as metabotropic mechanosensors in the nervous system and other organs. aGPCR are heavily spliced forecasting an extraordinary molecular structural diversity. Many predicted isoforms lack the transmembrane (7TM) signaling subunit, but to what extent these non-GPCR isoforms are produced and what physiological purpose they serve is unknown. Alternative splicing through intron retention ofADGRL/Latrophilin/CirlmRNA inDrosophilagenerates transcripts encoding unconventional proteins with an extracellular domain anchored by a single transmembrane helix (Cirl1TM). Here, we show thatCirl1TMtranscripts are translatedin vivoand that Cirl1TMbinds Cirl7TMN-terminal fragment-dependently. This interaction enables mechanosensory neurons to distinguish input intensities through Gαo-dependent signaling. Similarly, a direct interaction was found for mammalian GPR126/ADGRG6 isoforms. Together, our findings define intron retention and isoform-specific heteromerization as extraordinary molecular strategies to adjustCirl-dependent mechanosensation and demonstrate physiological relevance of versatile aGPCR isoform repertoire to tune cellular responsiveness.

High-resolution analysis of individual Drosophila melanogaster larvae uncovers individual variability in locomotion and its neurogenetic modulation

“…This is in line with published accounts showing decreased but existent proprioceptive capability [ 42 ]. It will be interesting to study larval locomotion in animals that express genetically modified Cirl proteins or specific Cirl isoforms [ 56 ], and the ability of Cirl mutants to successfully reach goals such as odours or tastants despite their impairment in crawling.…”