The adhesion GPCR ADGRL2 engages Gα13 to enable epidermal differentiation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41252157.
- Also identified by DOI 10.1073/pnas.2508436122 and PMC identifier 12663980.
- Licence recorded as CC BY-NC-ND.
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Abstract
Homeostasis relies on signaling networks controlled by cell membrane receptors. Although G-protein-coupled receptors (GPCRs) are the largest family of transmembrane receptors, their specific roles in the epidermis are not fully understood. Dual CRISPR-Flow and single cell Perturb RNA-sequencing knockout screens of all epidermal GPCRs were thus performed, uncovering an essential requirement for adhesion GPCR ADGRL2 (latrophilin 2) in epidermal differentiation. Among potential downstream guanine nucleotide-binding G proteins, ADGRL2 selectively activated Gα13. Follow-up tissue knockouts verified that Gα13 is also required for epidermal differentiation. A cryoelectron microscopy structure in lipid nanodiscs showed that ADGRL2 engages with Gα13 at multiple interfaces, including via an interaction between ADGRL2 intracellular loop 3 and a Gα13-specific QQQ glutamine triplet sequence in its GTPase domain. In situ gene mutation of this interface sequence impaired epidermal differentiation, highlighting an essential new role for an ADGRL2-Gα13 axis in epidermal differentiation.
Medical subject headings
- Cell Differentiation
- Receptors, G-Protein-Coupled
- GTP-Binding Protein alpha Subunits, G12-G13
- Epidermis
- Receptors, Peptide
- Epidermal Cells