1. Signal-Mediated Dynamic Retention of Glycosyltransferases in the Golgi.
- Author
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Linna Tu, Tai, William C. S., Lu Chen, and Banfield, David K.
- Subjects
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GLYCOSYLTRANSFERASE genes , *GLYCOSYLTRANSFERASES , *ENZYMES , *GENES , *PROTEINS , *GLYCOPROTEINS , *MEMBRANE proteins , *BIOLOGICAL membranes , *CELL membranes - Abstract
Golgi-resident glycosyltransferases are a family of enzymes that sequentially modify glycoproteins in a subcompartment-specific manner. These type II integral membrane proteins are characterized by a short cytoptasmically exposed amino-terminal tail and a luminal enzymatic domain. The cytoplasmic tails play a role in the localization of glycosyltransferases, and coat protein complex I (COPI) vesicle-mediated retrograde transport is also involved in their Golgi localization. However, the tails of these enzymes lack known COPI-binding motifs. Here, we found that Vps74p bound to a pentameric motif present in the cytoplasmic tails of the majority of yeast Golgi-localized glycosyltransferases, as well as to COPI. We propose that Vps74p maintains the steady-state localization of Golgi glycosyltransferases dynamically, by promoting their incorporation into COPI-coated vesicles. [ABSTRACT FROM AUTHOR]
- Published
- 2008