Short transmembrane domains target type II proteins to the Golgi apparatus and type I proteins to the endoplasmic reticulum

Author:

Bian Claudie12,Marchetti Anna1,Dias Marco2,Perrin Jackie1,Cosson Pierre1ORCID

Affiliation:

1. University of Geneva 1 Department of Cell Physiology and Metabolism, Faculty of Medicine , , 1 Rue Michel Servet, 1211 Geneva 4 , Switzerland

2. Manufacturing Science and Technologies 2 , Biotech Department, Merck, Z.I. de l'Ouriettaz 150, 1170 Aubonne , Switzerland

Abstract

ABSTRACT Transmembrane domains (TMDs) contain information targeting membrane proteins to various compartments of the secretory pathway. In previous studies, short or hydrophilic TMDs have been shown to target membrane proteins either to the endoplasmic reticulum (ER) or to the Golgi apparatus. However, the basis for differential sorting to the ER and to the Golgi apparatus remained unclear. To clarify this point, we quantitatively analyzed the intracellular targeting of a collection of proteins exhibiting a single TMD. Our results reveal that membrane topology is a major targeting element in the early secretory pathway: type I proteins with a short TMD are targeted to the ER, and type II proteins to the Golgi apparatus. A combination of three features accounts for the sorting of simple membrane proteins in the secretory pathway: membrane topology, length and hydrophilicity of the TMD, and size of the cytosolic domain. By clarifying the rules governing sorting to the ER and to the Golgi apparatus, our study could revive the search for sorting mechanisms in the early secretory pathway.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Merck

Université de Genève

Publisher

The Company of Biologists

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