Characterization of TSET, an ancient and widespread membrane trafficking complex

Author:

Hirst Jennifer1,Schlacht Alexander2,Norcott John P3,Traynor David4,Bloomfield Gareth4,Antrobus Robin1,Kay Robert R4,Dacks Joel B2,Robinson Margaret S1

Affiliation:

1. Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom

2. Department of Cell Biology, University of Alberta, Edmonton, Canada

3. Department of Engineering, University of Cambridge, Cambridge, United Kingdom

4. Cell Biology, MRC Laboratory of Molecular Biology, Cambridge, United Kingdom

Abstract

The heterotetrameric AP and F-COPI complexes help to define the cellular map of modern eukaryotes. To search for related machinery, we developed a structure-based bioinformatics tool, and identified the core subunits of TSET, a 'missing link' between the APs and COPI. Studies in Dictyostelium indicate that TSET is a heterohexamer, with two associated scaffolding proteins. TSET is non-essential in Dictyostelium, but may act in plasma membrane turnover, and is essentially identical to the recently described TPLATE complex, TPC. However, whereas TPC was reported to be plant-specific, we can identify a full or partial complex in every eukaryotic supergroup. An evolutionary path can be deduced from the earliest origins of the heterotetramer/scaffold coat to its multiple manifestations in modern organisms, including the mammalian muniscins, descendants of the TSET medium subunits. Thus, we have uncovered the machinery for an ancient and widespread pathway, which provides new insights into early eukaryotic evolution.

Funder

The Wellcome Trust

Medical Research Council

Alberta Innovates Technology Futures

Natural Sciences and Engineering Research Council of Canada

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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