Evidence map›Paper›PMID 25987606›Full record

ArticleThe Journal of cell biology2015

Ltc1 is an ER-localized sterol transporter and a component of ER-mitochondria and ER-vacuole contacts.

Andrew Murley, Reta D Sarsam, Alexandre Toulmay, Justin Yamada, William A Prinz, Jodi Nunnari

Abstract read
In one paragraph

Article in The Journal of cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 160 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed, 1 pooled it
–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

160 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. bioRxiv : the preprint server for biology · 2026
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100 more citing papers are in PubMed but not listed here.

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.

Andrew MurleyDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616.
Reta D SarsamDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616.
Alexandre ToulmayNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.
Justin YamadaDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616.
William A PrinzNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.
Jodi NunnariDepartment of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616 jmnunnari@ucdavis.edu.

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Intracellular Lipid Trafficking and Organelle BiogenesisZIADK060004 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI PRINZ, WILLIAM · 2009 to 2022
$8.5M
Biogenesis of the endoplasmic reticulumZIADK060105 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI PRINZ, WILLIAM · 2009 to 2022
$8.5M
The Mechanism of Mitochondrial Fission and Fusion.R01GM062942 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI NUNNARI, JODI M. · 2001 to 2013
$3.9M
Supplement Request for High throughput Image Analysis SystemR37GM097432 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NUNNARI, JODI M. · 2015 to 2020
$2.4M
Mechanisms controlling mitochondrial division and positioningR01GM097432 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NUNNARI, JODI M. · 2011 to 2014
$1.2M
Supplement to: PHYSICAL AND FUNCTIONAL SYSTEMS ANALYSIS OF MAMMALIAN MITOCHONDRIAR01GM106019 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BABU, MOHAN, NUNNARI, JODI M. · 2013 to 2016
$954k
NIGMS NIH HHS 5T32GM007377-34NIGMS NIH HHS R01 GM062942NIGMS NIH HHS R01GM062942NIGMS NIH HHS R01 GM097432NIGMS NIH HHS R01GM097432NIGMS NIH HHS R01 GM106019NIGMS NIH HHS R01GM106019NIGMS NIH HHS R37 GM097432NIGMS NIH HHS T32 GM007377
6 · The paper itself

Abstract

Organelle contact sites perform fundamental functions in cells, including lipid and ion homeostasis, membrane dynamics, and signaling. Using a forward proteomics approach in yeast, we identified new ER-mitochondria and ER-vacuole contacts specified by an uncharacterized protein, Ylr072w. Ylr072w is a conserved protein with GRAM and VASt domains that selectively transports sterols and is thus termed Ltc1, for Lipid transfer at contact site 1. Ltc1 localized to ER-mitochondria and ER-vacuole contacts via the mitochondrial import receptors Tom70/71 and the vacuolar protein Vac8, respectively. At mitochondria, Ltc1 was required for cell viability in the absence of Mdm34, a subunit of the ER-mitochondria encounter structure. At vacuoles, Ltc1 was required for sterol-enriched membrane domain formation in response to stress. Increasing the proportion of Ltc1 at vacuoles was sufficient to induce sterol-enriched vacuolar domains without stress. Thus, our data support a model in which Ltc1 is a sterol-dependent regulator of organelle and cellular homeostasis via its dual localization to ER-mitochondria and ER-vacuole contact sites.

Indexed as

AntiportersEndoplasmic ReticulumErgosterolIntracellular MembranesMitochondriaProtein TransportSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionSterol Regulatory Element Binding Protein 2Stress, PhysiologicalVacuolesAntiportersErgosterolLTC1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSterol Regulatory Element Binding Protein 2

Identifiers

PMID25987606
PMCPMC4442815

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.