The UDP-glycosyltransferase (UGT) superfamily expressed in humans, insects and plants: Animal-plant arms-race and co-evolution

被引:168
作者
Bock, Karl Walter [1 ]
机构
[1] Inst Expt & Clin Pharmacol & Toxicol, Dept Toxicol, Wilhelmstr 56, D-72074 Tubingen, Germany
关键词
UDP-glycosyltransferases; Humans; Phytoalexins; Quercetin; Glucosinolates; ARYL-HYDROCARBON RECEPTOR; GLUCOSYLTRANSFERASE ACTIVITY; FUNCTIONAL EXPRESSION; NOMENCLATURE UPDATE; XENOBIOTIC RESPONSE; CRYSTAL-STRUCTURE; MULTIGENE FAMILY; DRUG-METABOLISM; GLUCURONOSYLTRANSFERASE; QUERCETIN;
D O I
10.1016/j.bcp.2015.10.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
UDP-glycosyltransferases (UGTs) are major phase II enzymes of a detoxification system evolved in all kingdoms of life. Lipophilic endobiotics such as hormones and xenobiotics including phytoalexins and drugs are conjugated by vertebrates mainly with glucuronic acid, by invertebrates and plants mainly with glucose. Plant-herbivore arms-race has been the major driving force for evolution of large UGT and other enzyme superfamilies. The UGT superfamily is defined by a common protein structure and signature sequence of 44 amino acids responsible for binding the UDP moiety of the sugar donor. Plants developed toxic phytoalexins stored as glucosides. Upon herbivore attack these conjugates are converted to highly reactive compounds. In turn, animals developed large families of UGTs in their intestine and liver to detoxify these phytoalexins. Interestingly, phytoalexins, exemplified by quercetin glucuronides and glucosinolate-derived isocyanates, are known insect attractant pigments in plants, and antioxidants, anti-inflammatory and chemopreventive compounds of humans. It is to be anticipated that phytochemicals may provide a rich source in beneficial drugs. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:11 / 17
页数:7
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