Evidence map›Paper›PMID 30527664›Full record

ArticleMolecular cell2019

Spatially Distinct Pools of TORC1 Balance Protein Homeostasis.

Riko Hatakeyama, Marie-Pierre Péli-Gulli, Zehan Hu, Malika Jaquenoud, Guillermo Miguel Garcia Osuna, Alessandro Sardu, Jörn Dengjel, Claudio De Virgilio

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Molecular cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
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

63 citing papers in PubMed, 135 citations in OpenAlex.

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  19. The emerging mechanisms and functions of microautophagy.Nature reviews. Molecular cell biology · 2023
    Review
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3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Riko HatakeyamaDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland.
Marie-Pierre Péli-GulliDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland.
Zehan HuDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland.
Malika JaquenoudDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland.
Guillermo Miguel Garcia OsunaDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland.
Alessandro SarduDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland.
Jörn DengjelDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland; Department of Dermatology, Medical Center, University of Freiburg, 79104 Freiburg, Germany.
Claudio De VirgilioDepartment of Biology, University of Fribourg, 1700 Fribourg, Switzerland. Electronic address: claudio.devirgilio@unifr.ch.
University of Fribourg · CHUniversity Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The eukaryotic TORC1 kinase is a homeostatic controller of growth that integrates nutritional cues and mediates signals primarily from the surface of lysosomes or vacuoles. Amino acids activate TORC1 via the Rag GTPases that combine into structurally conserved multi-protein complexes such as the EGO complex (EGOC) in yeast. Here we show that Ego1, which mediates membrane-anchoring of EGOC via lipid modifications that it acquires while traveling through the trans-Golgi network, is separately sorted to vacuoles and perivacuolar endosomes. At both surfaces, it assembles EGOCs, which regulate spatially distinct pools of TORC1 that impinge on functionally divergent effectors: vacuolar TORC1 predominantly targets Sch9 to promote protein synthesis, whereas endosomal TORC1 phosphorylates Atg13 and Vps27 to inhibit macroautophagy and ESCRT-driven microautophagy, respectively. Thus, the coordination of three key regulatory nodes in protein synthesis and degradation critically relies on a division of labor between spatially sequestered populations of TORC1.

Indexed as

ProteostasisAdaptor Proteins, Signal TransducingAutophagyAutophagy-Related ProteinsEndosomal Sorting Complexes Required for TransportEndosomesGene Expression Regulation, FungalProtein Serine-Threonine KinasesProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionTranscription FactorsVacuolesAdaptor Proteins, Signal TransducingATG13 protein, S cerevisiaeAutophagy-Related ProteinsEndosomal Sorting Complexes Required for TransportMEH1 protein, S cerevisiaeProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsSCH9 protein, S cerevisiaeTORC1 protein complex, S cerevisiaeTranscription FactorsVPS27 protein, S cerevisiaeamino acid signalingAtg13endosomal sorting complex required for transportESCRTgrowth controlmacroautophagymicroautophagyprotein homeostasisRag GTPasestarget of rapamycin complex 1TORC1Vps27

Identifiers

PMID30527664
OpenAlexW2904301383

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.