Identification of a VPS29 isoform with restricted association to Retriever and Retromer accessory proteins through autoinhibition

The endosomal-lysosomal network is a hub of organelles that orchestrate the dynamic sorting of hundreds of integral membrane proteins to maintain cellular homeostasis. VPS29 is a central conductor of this network through its assembly into Retromer, Retriever, and Commander endosomal sorting complexes, and its role in regulating RAB GTPase activity. Two VPS29 isoforms have been described, VPS29A and VPS29B, that differ solely in their amino-terminal sequences. Here, we identify a third VPS29 isoform, which we term VPS29C, that harbors an extended amino-terminal sequence compared to VPS29A and VPS29B. Through a combination of AlphaFold predictive modeling, in vitro complex reconstitution, mass spectrometry, and molecular cell biology, we find that the amino-terminal VPS29C extension constitutes an autoinhibitory sequence that limits access to a hydrophobic groove necessary for effector protein recruitment to Retromer, and association with Retriever and Commander. VPS29C is therefore unique in its ability to uncouple Retromer-dependent cargo sorting from the broader roles of VPS29A and VPS29B in regulating the endosomal-lysosomal network through accessory protein recruitment. Our identification and characterization of VPS29C points to additional complexity in the differential subunit assembly of Retromer, an important consideration given the increasing interest in Retromer as a potential therapeutic target in neurodegenerative diseases.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-06-30
DOI
https://doi.org/10.1073/pnas.2501111122
Citations
2
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
2.30

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article

Identification of a VPS29 isoform with restricted association to Retriever and Retromer accessory proteins through autoinhibition

Rebeka Butkovič, Edmund R. R. Moody, James L. Daly, Philip A. Lewis et al.
2 citations
Proceedings of the National Academy of Sciences
Cellular transport and secretion
2.30
article

Identification of a VPS29 isoform with restricted association to Retriever and Retromer accessory proteins through autoinhibition

Rebeka Butkovič, Edmund R. R. Moody, James L. Daly, Philip A. Lewis, Brett M. Collins, Michael D. Healy, Peter J. Cullen, Qian Guo, Kate J. Heesom, Kirsty J. McMillan, Kai‐En Chen, Tom A. Williams, Eva Pennink, Georgia Gamble-Strutt, Zara Higham
article en
2 citations

Abstract

The endosomal-lysosomal network is a hub of organelles that orchestrate the dynamic sorting of hundreds of integral membrane proteins to maintain cellular homeostasis. VPS29 is a central conductor of this network through its assembly into Retromer, Retriever, and Commander endosomal sorting complexes, and its role in regulating RAB GTPase activity. Two VPS29 isoforms have been described, VPS29A and VPS29B, that differ solely in their amino-terminal sequences. Here, we identify a third VPS29 isoform, which we term VPS29C, that harbors an extended amino-terminal sequence compared to VPS29A and VPS29B. Through a combination of AlphaFold predictive modeling, in vitro complex reconstitution, mass spectrometry, and molecular cell biology, we find that the amino-terminal VPS29C extension constitutes an autoinhibitory sequence that limits access to a hydrophobic groove necessary for effector protein recruitment to Retromer, and association with Retriever and Commander. VPS29C is therefore unique in its ability to uncouple Retromer-dependent cargo sorting from the broader roles of VPS29A and VPS29B in regulating the endosomal-lysosomal network through accessory protein recruitment. Our identification and characterization of VPS29C points to additional complexity in the differential subunit assembly of Retromer, an important consideration given the increasing interest in Retromer as a potential therapeutic target in neurodegenerative diseases.

Proceedings of the National Academy of SciencesVol. 122(27)
Guy's Hospital (GB), University of Liverpool (GB), The University of Queensland (AU), King's College London (GB), University of Bristol (GB), Systems Biology Institute (JP), Health & Life (Taiwan) (TW)
Wellcome Trust, Royal Society, University College London, University of Bristol, Lister Institute of Preventive Medicine, Medical Research Council, European Research Council, National Health and Medical Research Council
Openalex Percentile: Top 13%
Cellular transport and secretion
2.30
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