A naturally occurring membrane-anchored Gαs variant, XLαs, activates phospholipase Cβ4

• Published in: The Journal of biological chemistry 2022-08, Vol.298 (8), p.102134-102134, Article 102134
• Main Authors: Phan, Hoa T.N., Loomis, Joseph, Abraham, Saji, He, Qing, Bastepe, Murat, Smrcka, Alan V.
• Format: Article
• Language: English
• Subjects: adenylate cyclase; Cell Membrane - metabolism; G protein; G protein–coupled receptor; GTP-Binding Protein alpha Subunits, Gs - metabolism; Gαs; inositol phosphate; Inositol Phosphates - metabolism; Isoenzymes - metabolism; Isoproterenol - pharmacology; phospholipase C; Phospholipase C beta - metabolism; plasma membrane targeting; signal transduction
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2022.102134

Extra-large stimulatory Gα (XLαs) is a large variant of G protein αs subunit (Gαs) that uses an alternative promoter and thus differs from Gαs at the first exon. XLαs activation by G protein–coupled receptors mediates cAMP generation, similarly to Gαs; however, Gαs and XLαs have been shown to have distinct cellular and physiological functions. For example, previous work suggests that XLαs can stimulate inositol phosphate production in renal proximal tubules and thereby regulate serum phosphate levels. In this study, we show that XLαs directly and specifically stimulates a specific isoform of phospholipase Cβ (PLCβ), PLCβ4, both in transfected cells and with purified protein components. We demonstrate that neither the ability of XLαs to activate cAMP generation nor the canonical G protein switch II regions are required for PLCβ stimulation. Furthermore, this activation is nucleotide independent but is inhibited by Gβγ, suggesting a mechanism of activation that relies on Gβγ subunit dissociation. Surprisingly, our results indicate that enhanced membrane targeting of XLαs relative to Gαs confers the ability to activate PLCβ4. We also show that PLCβ4 is required for isoproterenol-induced inositol phosphate accumulation in osteocyte-like Ocy454 cells. Taken together, we demonstrate a novel mechanism for activation of phosphoinositide turnover downstream of Gs-coupled receptors that may have a critical role in endocrine physiology.