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一种新的人类糖皮质激素受体单核苷酸多态性导致转录激活潜能增加。

A novel human glucocorticoid receptor SNP results in increased transactivation potential.

作者信息

Green Tajia L, Tung Kelly, Lim Debora, Leventhal Stacey M, Cho Kiho, Greenhalgh David G

机构信息

Shriners Hospitals for Children Northern California, and Department of Surgery, University of California, Davis, Sacramento, CA 95817, USA.

出版信息

Biochem Biophys Rep. 2016 Dec 18;9:140-145. doi: 10.1016/j.bbrep.2016.12.003. eCollection 2017 Mar.

Abstract

Glucocorticoids are one of the most widely used therapeutics in the treatment of a variety of inflammatory disorders. However, it is known that there are variable patient responses to glucocorticoid treatment; there are responders and non-responders, or those that need higher dosages. Polymorphisms in the glucocorticoid receptor (GR) have been implicated in this variability. In this study, ninety-seven volunteers were surveyed for polymorphisms in the human GR-alpha (hGRα), the accepted biologically active reference isoform. One isoform identified in our survey, named hGR DL-2, had four single nucleotide polymorphisms (SNPs), one synonymous and three non-synonymous, and a four base pair deletion resulting in a frame shift and early termination to produce a 743 amino acid putative protein. hGR DL-2 had a decrease in transactivation potential of more than 90%. Upon further analysis of the individual SNPs and deletion, one SNP, A829G, which results in a lysine to glutamic acid amino acid change at position 277, was found to increase the transactivation potential of hGR more than eight times the full-length reference. Furthermore, the hGRα-A829G isoform had a differential hyperactive response to various exogenous steroids. Increasing our knowledge as to how various SNPs affect hGR activity may help in understanding the unpredictable patient response to steroid treatment, and is a step towards personalizing patient care.

摘要

糖皮质激素是治疗多种炎症性疾病最广泛使用的疗法之一。然而,已知患者对糖皮质激素治疗的反应存在差异;有反应者和无反应者,或者那些需要更高剂量的患者。糖皮质激素受体(GR)的多态性与这种变异性有关。在本研究中,对97名志愿者的人GR-α(hGRα)(公认的具有生物活性的参考异构体)的多态性进行了调查。我们的调查中鉴定出的一种异构体,命名为hGR DL-2,有四个单核苷酸多态性(SNP),一个同义突变和三个非同义突变,以及一个四碱基对缺失,导致移码和提前终止,产生一个743个氨基酸的推定蛋白。hGR DL-2的反式激活潜能降低了90%以上。在对单个SNP和缺失进行进一步分析时,发现一个SNP,A829G,它导致第277位的赖氨酸到谷氨酸的氨基酸变化,使hGR的反式激活潜能增加到全长参考的八倍以上。此外,hGRα-A829G异构体对外源类固醇有不同的高反应性。增加我们对各种SNP如何影响hGR活性的了解,可能有助于理解患者对类固醇治疗不可预测的反应,并且是迈向个性化患者护理的一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1de/5614576/0ef8faddf8c9/gr1.jpg

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