Polypeptide N-acetylgalactosamine transferase 3: a post-translational writer on human health

被引:2
|
作者
Camila Garay, Yohana [1 ]
Beatriz Cejas, Romina [2 ]
Lorenz, Virginia [3 ]
Zlocowski, Natacha [4 ]
Parodi, Pedro [1 ]
Alejandro Ferrero, Franco [1 ]
Angeloni, Genaro [1 ]
Alfonso Garcia, Valentina [1 ]
German Sendra, Victor [5 ]
Dante Lardone, Ricardo [1 ]
Jose Irazoqui, Fernando [1 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Ctr Invest Quim Biol Cordoba, CIQUIBIC,CONICET, Ciudad Univ,X5000HUA, Cordoba, Argentina
[2] Northwestern Univ, Dept Pharmacol, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Univ Nacl Litoral UNL, Fac Bioquim & Ciencias Biol, Inst Salud & Ambiente Litoral ISAL, Consejo Nacl Invest Cient & Tecn CONICET, Santa Fe, Argentina
[4] Univ Nacl Cordoba, Fac Ciencias Med, Ctr Microscopia Elect, Inst Invest Ciencias Salud INICSA CONICET, Cordoba, Argentina
[5] Tufts Univ, Sch Med, Ctr Translat Ocular Immunol, Dept Ophthalmol,Tufts Med Ctr, Boston, MA 02111 USA
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2022年 / 100卷 / 10期
关键词
Glycobiology; Glycosyltransferases; O-Glycans; Post-translational modifications; Potential therapies; UDP-GALNAC-POLYPEPTIDE; ALPHA-D-GALACTOSAMINE; O-LINKED GLYCOSYLATION; LECTIN DOMAIN; CDNA CLONING; GLYCOSYLTRANSFERASE COMPLEXES; MOLECULAR-CLONING; CRYSTAL-STRUCTURE; EXPRESSION; CANCER;
D O I
10.1007/s00109-022-02249-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Polypeptide N-acetylgalactosamine transferase 3 (ppGalNAc-T3) is an enzyme involved in the initiation of O-GalNAc glycan biosynthesis. Acting as a writer of frequent post-translational modification (PTM) on human proteins, ppGalNAc-T3 has key functions in the homeostasis of human cells and tissues. We review the relevant roles of this molecule in the biosynthesis of O-GalNAc glycans, as well as in biological functions related to human physiological and pathological conditions. With main emphasis in ppGalNAc-T3, we draw attention to the different ways involved in the modulation of ppGalNAc-Ts enzymatic activity. In addition, we take notice on recent reports of ppGalNAc-T3 having different subcellular localizations, highlight critical intrinsic and extrinsic functions in cellular physiology that are exerted by ppGalNAc-T3-synthesized PTMs, and provide an update on several human pathologies associated with dysfunctional ppGalNAc-T3. Finally, we propose biotechnological tools as new therapeutic options for the treatment of pathologies related to altered ppGalNAc-T3. Key messages ppGalNAc-T3 is a key enzyme in the human O-GalNAc glycans biosynthesis. enzyme activity is regulated by PTMs, lectin domain and protein-protein interactions. ppGalNAc-T3 is located in human Golgi apparatus and cell nucleus. ppGalNAc-T3 has a central role in cell physiology as well as in several pathologies. Biotechnological tools for pathological management are proposed.
引用
收藏
页码:1387 / 1403
页数:17
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