7ltw | pdb_00007ltw
Crystal structure of the mouse Kirrel2 D1 homodimer
Structural highlights
FunctionKIRR2_MOUSE May regulate basal insulin secretion.[1] Publication Abstract from PubMedProjections from sensory neurons of olfactory systems coalesce into glomeruli in the brain. The Kirrel receptors are believed to homodimerize via their ectodomains and help separate sensory neuron axons into Kirrel2- or Kirrel3-expressing glomeruli. Here, we present the crystal structures of homodimeric Kirrel receptors and show that the closely related Kirrel2 and Kirrel3 have evolved specific sets of polar and hydrophobic interactions, respectively, disallowing heterodimerization while preserving homodimerization, likely resulting in proper segregation and coalescence of Kirrel-expressing axons into glomeruli. We show that the dimerization interface at the N-terminal immunoglobulin (IG) domains is necessary and sufficient to create homodimers and fail to find evidence for a secondary interaction site in Kirrel ectodomains. Furthermore, we show that abolishing dimerization of Kirrel3 in vivo leads to improper formation of glomeruli in the mouse accessory olfactory bulb as observed in Kirrel3(-/-) animals. Our results provide evidence for Kirrel3 homodimerization controlling axonal coalescence. Molecular and structural basis of olfactory sensory neuron axon coalescence by Kirrel receptors.,Wang J, Vaddadi N, Pak JS, Park Y, Quilez S, Roman CA, Dumontier E, Thornton JW, Cloutier JF, Ozkan E Cell Rep. 2021 Nov 2;37(5):109940. doi: 10.1016/j.celrep.2021.109940. PMID:34731636[2] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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