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G蛋白偶联受体非同义自然变异的综合分析

Comprehensive Analysis of Non-Synonymous Natural Variants of G Protein-Coupled Receptors.

作者信息

Kim Hee Ryung, Duc Nguyen Minh, Chung Ka Young

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.

出版信息

Biomol Ther (Seoul). 2018 Mar 1;26(2):101-108. doi: 10.4062/biomolther.2017.073.

Abstract

G protein-coupled receptors (GPCRs) are the largest superfamily of transmembrane receptors and have vital signaling functions in various organs. Because of their critical roles in physiology and pathology, GPCRs are the most commonly used therapeutic target. It has been suggested that GPCRs undergo massive genetic variations such as genetic polymorphisms and DNA insertions or deletions. Among these genetic variations, non-synonymous natural variations change the amino acid sequence and could thus alter GPCR functions such as expression, localization, signaling, and ligand binding, which may be involved in disease development and altered responses to GPCR-targeting drugs. Despite the clinical importance of GPCRs, studies on the genotype-phenotype relationship of GPCR natural variants have been limited to a few GPCRs such as β-adrenergic receptors and opioid receptors. Comprehensive understanding of non-synonymous natural variations within GPCRs would help to predict the unknown genotype-phenotype relationship and yet-to-be-discovered natural variants. Here, we analyzed the non-synonymous natural variants of all non-olfactory GPCRs available from a public database, UniProt. The results suggest that non-synonymous natural variations occur extensively within the GPCR superfamily especially in the N-terminus and transmembrane domains. Within the transmembrane domains, natural variations observed more frequently in the conserved residues, which leads to disruption of the receptor function. Our analysis also suggests that only few non-synonymous natural variations have been studied in efforts to link the variations with functional consequences.

摘要

G蛋白偶联受体(GPCRs)是最大的跨膜受体超家族,在各个器官中具有重要的信号传导功能。由于其在生理和病理过程中的关键作用,GPCRs是最常用的治疗靶点。有人提出,GPCRs会发生大量的基因变异,如基因多态性以及DNA插入或缺失。在这些基因变异中,非同义自然变异会改变氨基酸序列,从而可能改变GPCR的功能,如表达、定位、信号传导和配体结合,这可能与疾病发展以及对GPCR靶向药物的反应改变有关。尽管GPCRs具有临床重要性,但关于GPCR自然变异体的基因型-表型关系的研究仅限于少数几种GPCRs,如β-肾上腺素能受体和阿片受体。全面了解GPCRs中的非同义自然变异将有助于预测未知的基因型-表型关系以及尚未发现的自然变异体。在此,我们分析了公共数据库UniProt中所有非嗅觉GPCRs的非同义自然变异体。结果表明,非同义自然变异在GPCR超家族中广泛存在,尤其是在N端和跨膜结构域。在跨膜结构域中,在保守残基中观察到的自然变异更为频繁,这会导致受体功能的破坏。我们的分析还表明,在将这些变异与功能后果联系起来的研究中,只对少数非同义自然变异进行了研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaf0/5839487/eb1ee0619aeb/bt-26-101f1.jpg

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