Evidence map›Paper›PMID 27074665›Full record

ArticleeLife2016

ESCRT-III activation by parallel action of ESCRT-I/II and ESCRT-0/Bro1 during MVB biogenesis.

Shaogeng Tang, Nicholas J Buchkovich, W Mike Henne, Sudeep Banjade, Yun Jung Kim, Scott D Emr

Abstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

55 citing papers in PubMed.

  1. Review
  2. ESCRT-III function in membrane fission and repair.Nature reviews. Molecular cell biology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Endocytic tethers modulate unconventional GAPDH secretion.Cell surface (Amsterdam, Netherlands) · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Vps60 initiates alternative ESCRT-III filaments.The Journal of cell biology · 2023
    Article
  15. Tissue-specific knockout inbioRxiv : the preprint server for biology · 2023
    Article
  16. Article
  17. Article
  18. The Machinery of Exosomes: Biogenesis, Release, and Uptake.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Bro1 family proteins harmonize cargo sorting with vesicle formation.BioEssays : news and reviews in molecular, cellular and developmental biology · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Shaogeng TangWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States.ORCID 0000-0002-3904-492X
Nicholas J BuchkovichWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States.
W Mike HenneWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States.
Sudeep BanjadeWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States.
Yun Jung KimWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States.
Scott D EmrWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, United States.ORCID 0000-0002-5408-6781

Funding

PREDOCTORAL TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM007273 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BRETSCHER, ANTHONY P. · 1985 to 2019
$11.6M
NIGMS NIH HHS T32 GM007273
6 · The paper itself

Abstract

The endosomal sorting complexes required for transport (ESCRT) pathway facilitates multiple fundamental membrane remodeling events. Previously, we determined X-ray crystal structures of ESCRT-III subunit Snf7, the yeast CHMP4 ortholog, in its active and polymeric state (Tang et al., 2015). However, how ESCRT-III activation is coordinated by the upstream ESCRT components at endosomes remains unclear. Here, we provide a molecular explanation for the functional divergence of structurally similar ESCRT-III subunits. We characterize novel mutations in ESCRT-III Snf7 that trigger activation, and identify a novel role of Bro1, the yeast ALIX ortholog, in Snf7 assembly. We show that upstream ESCRTs regulate Snf7 activation at both its N-terminal core domain and the C-terminus α6 helix through two parallel ubiquitin-dependent pathways: the ESCRT-I-ESCRT-II-Vps20 pathway and the ESCRT-0-Bro1 pathway. We therefore provide an enhanced understanding for the activation of the spatially unique ESCRT-III-mediated membrane remodeling.

Indexed as

Gene Expression Regulation, FungalCell MembraneEndosomal Sorting Complexes Required for TransportMultivesicular BodiesMutationProtein DomainsProtein Structure, SecondaryProtein TransportSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionUbiquitinated ProteinsUbiquitinationBro1 protein, S cerevisiaeEndosomal Sorting Complexes Required for TransportSaccharomyces cerevisiae ProteinsSNF7 protein, S cerevisiaeUbiquitinated ProteinsactivationbiochemistryBro1cell biologyESCRT-IESCRT-IIESCRT-IIIS. cerevisiaeSnf7

Identifiers

PMID27074665
PMCPMC4865371

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.