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Anatomical Profiling of G Protein-Coupled Receptor Expression

机译:G蛋白偶联受体表达的解剖学分析

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G protein-coupled receptors (GPCRs) comprise the largest family of transmembrane signaling molecules and regulate a host of physiological and disease processes. To better understand the functions of GPCRs in vivo, we quantified transcript levels of 353 nonodorant GPCRs in 41 adult mouse tissues. Cluster analysis placed many GPCRs into anticipated anatomical and functional groups and predicted previously unidentified roles for less-studied receptors. From one such prediction, we showed that the Gpr91 ligand succinate can regulate lipolysis in white adipose tissue, suggesting that signaling by this citric acid cycle intermediate may regulate energy homeostasis. We also showed that pairwise analysis of GPCR expression across tissues may help predict drug side effects. This resource will aid studies to understand GPCR function in vivo and may assist in the identification of therapeutic targets.
机译:G蛋白偶联受体(GPCR)包含最大的跨膜信号传导分子系列,并调节一系列生理和疾病过程。 为了更好地了解GPCR在体内GPCR的功能,我们在41个成年小鼠组织中量化了353个非富集GPCR的转录水平。 簇分析将许多GPCR放入预期的解剖学和官能团中,并预测以前过于研究的受体的未识别的作用。 从一种这样的预测中,我们表明GPR91配体琥珀酸盐可以调节白色脂肪组织中的脂解,表明该柠檬酸循环中间体的信号传导可以调节能量稳态。 我们还表明,对组织的GPCR表达的成对分析可能有助于预测药物副作用。 该资源将帮助研究了解体内GPCR功能,并有助于识别治疗目标。

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