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仅含F-box结构域蛋白44通过泛素化和降解作用调节孕烷X受体蛋白水平。

The F-box-only protein 44 regulates pregnane X receptor protein level by ubiquitination and degradation.

作者信息

Florke Gee Rebecca R, Huber Andrew D, Wu Jing, Bajpai Richa, Loughran Allister J, Pruett-Miller Shondra M, Chen Taosheng

机构信息

Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Graduate School of Biomedical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

Acta Pharm Sin B. 2023 Nov;13(11):4523-4534. doi: 10.1016/j.apsb.2023.07.014. Epub 2023 Jul 20.

DOI:10.1016/j.apsb.2023.07.014
PMID:37969738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10638512/
Abstract

Pregnane X receptor (PXR) is a ligand-activated nuclear receptor that transcriptionally upregulates drug-metabolizing enzymes [.., cytochrome P450 3A4 (CYP3A4)] and transporters. Although the regulation of PXR target genes is well-characterized, less is known about the regulation of PXR protein level. By screening an RNAi library, we identified the F-box-only protein 44 (FBXO44) as a novel E3 ligase for PXR. PXR abundance increases upon knockdown of FBXO44, and, inversely, decreases upon overexpression of FBXO44. Further analysis revealed that FBXO44 interacts with PXR, leading to its ubiquitination and proteasomal degradation, and we determined that the F-box associated domain of FBXO44 and the ligand binding domain of PXR are required for the functional interaction. In summary, FBXO44 regulates PXR protein abundance, which has downstream consequences for levels and drug-drug interactions. The results of this study provide new insight into the molecular mechanisms that regulate PXR protein level and activity and suggest the importance of considering how modulating E3 ubiquitin ligase activities will affect PXR-mediated drug metabolism.

摘要

孕烷X受体(PXR)是一种配体激活的核受体,可转录上调药物代谢酶[如细胞色素P450 3A4(CYP3A4)]和转运蛋白。尽管对PXR靶基因的调控已得到充分表征,但对PXR蛋白水平的调控了解较少。通过筛选RNAi文库,我们鉴定出仅含F盒蛋白44(FBXO44)是PXR的一种新型E3连接酶。敲低FBXO44后PXR丰度增加,反之,过表达FBXO44后PXR丰度降低。进一步分析表明,FBXO44与PXR相互作用,导致其泛素化和蛋白酶体降解,并且我们确定FBXO44的F盒相关结构域和PXR的配体结合结构域是功能相互作用所必需的。总之,FBXO44调节PXR蛋白丰度,这对[相关物质]水平和药物-药物相互作用具有下游影响。本研究结果为调节PXR蛋白水平和活性的分子机制提供了新的见解,并表明考虑调节E3泛素连接酶活性如何影响PXR介导的药物代谢的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/5a58e7780e0b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/3294bf99ef60/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/d5323ab8bd9b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/d4a8dab86d72/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/8e929f2ac452/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/c1c9b09c07b6/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/f9567c6debea/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/5a58e7780e0b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/3294bf99ef60/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/d5323ab8bd9b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/d4a8dab86d72/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/8e929f2ac452/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/c1c9b09c07b6/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/f9567c6debea/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df09/10638512/5a58e7780e0b/gr6.jpg

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