4.6 Review Book Chapter

The Biochemistry of O-GlcNAc Transferase: Which Functions Make It Essential in Mammalian Cells?

期刊

ANNUAL REVIEW OF BIOCHEMISTRY, VOL 85
卷 85, 期 -, 页码 631-657

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev-biochem-060713-035344

关键词

O-linked N-acetylglucosamine transferase; OGT structure; glycosyltransferase mechanism; nutrient sensing; O-GlcNAcylation; host cell factor 1; HCF-1; tetratricopeptide repeat; TPR

资金

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM095450, R01GM094263, T32GM007306] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [R01 GM094263, T32 GM007306] Funding Source: Medline

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O-linked N-acetylglucosamine transferase (OGT) is found in all metazoans and plays an important role in development but at the single-cell level is only essential in dividing mammalian cells. Postmitotic mammalian cells and cells of invertebrates such as Caenorhabditis elegans and Drosophila can survive without copies of OGT. Why OGT is required in dividing mammalian cells but not in other cells remains unknown. OGT has multiple biochemical activities. Beyond its well-known role in adding beta-O-GlcNAc to serine and threonine residues of nuclear and cytoplasmic proteins, OGT also acts as a protease in the maturation of the cell cycle regulator host cell factor 1 (HCF-1) and serves as an integral member of several protein complexes, many of them linked to gene expression. In this review, we summarize current understanding of the mechanisms underlying OGT's biochemical activities and address whether known functions of OGT could be related to its essential role in dividing mammalian cells.

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