Evidence map›Paper›PMID 26569496›Full record

ArticleAutophagy2015

TOR-dependent post-transcriptional regulation of autophagy.

Guowu Hu, Travis McQuiston, Amélie Bernard, Yoon-Dong Park, Jin Qiu, Ali Vural, Nannan Zhang, Scott R Waterman, Nathan H Blewett, Timothy G Myers and 5 more

Open access · bronzeAbstract readComment
In one paragraph

Article in Autophagy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Gentirigeoside B fromAntioxidants (Basel, Switzerland) · 2022
    Article
  2. miR-151 Affects Low-Temperature Tolerance ofFrontiers in cell and developmental biology · 2021
    Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Guowu Hua Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Travis McQuistona Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Amélie Bernardb Life Sciences Institute; University of Michigan ; Ann Arbor , MI USA.
Yoon-Dong Parka Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Jin Qiua Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Ali Vuralc Laboratory of Immunoregulation; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Nannan Zhanga Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Scott R Watermana Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Nathan H Blewettd Intramural Research Program in Genomics of Differentiation; National Institute of Child Health and Human Development; National Institutes of Health ; Bethesda , MD USA.
Timothy G Myerse Genomic Technologies Section; Research Technologies Branch; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Richard J Maraiad Intramural Research Program in Genomics of Differentiation; National Institute of Child Health and Human Development; National Institutes of Health ; Bethesda , MD USA.
John H Kehrlc Laboratory of Immunoregulation; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Gulbu Uzela Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
Daniel J Klionskyb Life Sciences Institute; University of Michigan ; Ann Arbor , MI USA.
Peter R Williamsona Laboratory of Clinical Infectious Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health ; Bethesda , MD USA.
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversity of Michigan–Ann Arbor · US

Funding

Infectious Diseases Research Technologies Core - BethesdaZICAI001051 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHERRY, JAMES · 2009 to 2025
$226.1M
Molecular Regulation Of RNA MetabolismZIAHD000412 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI MARAIA, RICHARD J · 2009 to 2025
$31.6M
Signal Transduction In B Lymphocytes: Identification Of Key Signaling MoleculesZIAAI000739 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KEHRL, JOHN H · 2009 to 2025
$17.8M
ALTERNATIVE VACUOLAR TARGETING MECHANISMS IN YEASTR01GM053396 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KLIONSKY, DANIEL J. · 1995 to 2018
$12.1M
Molecular Pathobiology of Cryptococcus neoformansZIAAI001123 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI WILLIAMSON, PETER · 2010 to 2025
$10.4M
Translational Research: Host-Pathogen Interactions in Patient Fungal DiseasesZIAAI001124 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI WILLIAMSON, PETER · 2010 to 2025
$8.8M
NIGMS NIH HHS GM053396NIGMS NIH HHS R01 GM053396
6 · The paper itself

Abstract

Regulation of autophagy is required to maintain cellular equilibrium and prevent disease. While extensive study of post-translational mechanisms has yielded important insights into autophagy induction, less is known about post-transcriptional mechanisms that could potentiate homeostatic control. In our study, we showed that the RNA-binding protein, Dhh1 in Saccharomyces cerevisiae and Vad1 in the pathogenic yeast Cryptococcus neoformans is involved in recruitment and degradation of key autophagy mRNAs. In addition, phosphorylation of the decapping protein Dcp2 by the target of rapamycin (TOR), facilitates decapping and degradation of autophagy-related mRNAs, resulting in repression of autophagy under nutrient-replete conditions. The post-transcriptional regulatory process is conserved in both mouse and human cells and plays a role in autophagy-related modulation of the inflammasome product IL1B. These results were then applied to provide mechanistic insight into autoimmunity of a patient with a PIK3CD/p110δ gain-of-function mutation. These results thus identify an important new post-transcriptional mechanism of autophagy regulation that is highly conserved between yeast and mammals.

Indexed as

AnimalsAutophagyDEAD-box RNA HelicasesFemaleHumansRNA StabilitySaccharomyces cerevisiae ProteinsDEAD-box RNA HelicasesSaccharomyces cerevisiae ProteinsautoimmunityautophagyphosphorylationTORtranslation

Identifiers

PMID26569496
PMCPMC4835197
OpenAlexW2233080663

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.