Mohammad Ali Mohammad Nezhady, Gael Cagnone, Emmanuel Bajon, Prabhas Chaudhari, Monir Modaresinejad, Pierre Hardy, Damien Maggiorani, Christiane Quiniou, Jean-Sébastien Joyal, Christian Beauséjour, Sylvain Chemtob
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引用次数: 0
摘要
G 蛋白偶联受体(GPCR)几乎参与了每一个生理过程。然而,它们能够调控大量不同过程的机制仍然难以捉摸。一种非常规的功能模式至少可以部分解释这种多样化的参与,但这种模式还有待探索。我们发现,多功能乳酸 GPCR HCAR1 定位于细胞核,能够启动基于位置的信号传导,特别是核-ERK 和 AKT。我们发现,核 HCAR1(N-HCAR1)直接参与调节多种过程。具体来说,N-HCAR1 与参与促进蛋白质翻译、核糖体生物生成和 DNA 损伤修复的蛋白质复合物结合。N-HCAR1 还与染色质重塑因子相互作用,直接调控基因表达。我们发现,N-HCAR1 比其质膜对应物显示出更广泛的转录组特征。有趣的是,从细胞核中排除 HCAR1 对体内肿瘤生长和转移的影响与从细胞中完全清除 HCAR1 对肿瘤生长和转移的影响相同。这些结果揭示了细胞核定位 GPCR 的非经典功能,这些功能有别于传统的受体模式,HCAR1 可通过这些功能参与调节各种细胞过程。
Unconventional receptor functions and location-biased signaling of the lactate GPCR in the nucleus.
G-protein-coupled receptors (GPCRs) are virtually involved in every physiological process. However, mechanisms for their ability to regulate a vast array of different processes remain elusive. An unconventional functional modality could at least in part account for such diverse involvements but has yet to be explored. We found HCAR1, a multifunctional lactate GPCR, to localize at the nucleus and therein capable of initiating location-biased signaling notably nuclear-ERK and AKT. We discovered that nuclear HCAR1 (N-HCAR1) is directly involved in regulating diverse processes. Specifically, N-HCAR1 binds to protein complexes that are involved in promoting protein translation, ribosomal biogenesis, and DNA-damage repair. N-HCAR1 also interacts with chromatin remodelers to directly regulate gene expression. We show that N-HCAR1 displays a broader transcriptomic signature than its plasma membrane counterpart. Interestingly, exclusion of HCAR1 from the nucleus has the same effect as its complete cellular depletion on tumor growth and metastasis in vivo. These results reveal noncanonical functions for a cell nucleus-localized GPCR that are distinct from traditional receptor modalities and through which HCAR1 can participate in regulating various cellular processes.
期刊介绍:
Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.