Kreppel L K, Blomberg M A, Hart G W
Department of Biochemistry and Molecular Genetics Schools of Medicine/Dentistry, University of Alabama at Birmingham Station, Birmingham, Alabama 35294, USA.
J Biol Chem. 1997 Apr 4;272(14):9308-15. doi: 10.1074/jbc.272.14.9308.
O-Linked N-acetylglucosamine (O-GlcNAc) glycosylation is a dynamic modification of eukaryotic nuclear and cytosolic proteins analogous to protein phosphorylation. We have cloned and characterized a novel gene for an O-GlcNAc transferase (OGT) that shares no sequence homology or structural similarities with other glycosyltransferases. The OGT gene is highly conserved (up to 80% identity) in all eukaryotes examined. Unlike previously described glycosyltransferases, OGT is localized to the cytosol and nucleus. The OGT protein contains multiple tandem repeats of the tetratricopeptide repeat motif. The presence of tetratricopeptide repeats, which can mediate protein-protein interactions, suggests that OGT may be regulated by protein interactions that are independent of the enzyme's catalytic site. The OGT is also modified by tyrosine phosphorylation, indicating that tyrosine kinase signal transduction cascades may play a role in modulating OGT activity.
O-连接的N-乙酰葡糖胺(O-GlcNAc)糖基化是真核细胞核蛋白和胞质蛋白的一种动态修饰,类似于蛋白质磷酸化。我们克隆并鉴定了一种新型的O-GlcNAc转移酶(OGT)基因,该基因与其他糖基转移酶没有序列同源性或结构相似性。OGT基因在所有检测的真核生物中高度保守(同一性高达80%)。与先前描述的糖基转移酶不同,OGT定位于胞质溶胶和细胞核。OGT蛋白包含多个四肽重复基序的串联重复序列。四肽重复序列的存在可以介导蛋白质-蛋白质相互作用,这表明OGT可能受独立于酶催化位点的蛋白质相互作用的调节。OGT也被酪氨酸磷酸化修饰,这表明酪氨酸激酶信号转导级联反应可能在调节OGT活性中发挥作用。