Evidence map›Paper›PMID 25332163›Full record

ArticleThe Journal of cell biology2014

Acinus integrates AKT1 and subapoptotic caspase activities to regulate basal autophagy.

Nilay Nandi, Lauren K Tyra, Drew Stenesen, Helmut Krämer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Guideline
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  7. Dronc-independent basal executioner caspase activity sustainsProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  15. Activated Acinus boosts basal autophagy.Molecular & cellular oncology
    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

4 authors at 1 institution in 1 country.

Nilay NandiDepartment of Neuroscience and Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Lauren K TyraDepartment of Neuroscience and Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Drew StenesenDepartment of Neuroscience and Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Helmut KrämerDepartment of Neuroscience and Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390 Department of Neuroscience and Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390 helmut.kramer@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
MOLECULAR ANALYSIS OF THE BOSS TRANSMEMBRANE LIGANDR01EY010199 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI Helmut J Kramer · 1994 to 2026
$9.7M
SEM for UT Southwestern EM Core FacilityS10OD020103 · OD · UT SOUTHWESTERN MEDICAL CENTER · PI LUBY-PHELPS, KATHERINE J · 2015 to 2015
$306k
NEI NIH HHS EY10199NEI NIH HHS R01 EY010199NIH HHS P40 OD018537NIH HHS S10 OD020103
6 · The paper itself

Abstract

How cellular stresses up-regulate autophagy is not fully understood. One potential regulator is the Drosophila melanogaster protein Acinus (Acn), which is necessary for autophagy induction and triggers excess autophagy when overexpressed. We show that cell type-specific regulation of Acn depends on proteolysis by the caspase Dcp-1. Basal Dcp-1 activity in developing photoreceptors is sufficient for this cleavage without a need for apoptosis to elevate caspase activity. On the other hand, Acn was stabilized by loss of Dcp-1 function or by the presence of a mutation in Acn that eliminates its conserved caspase cleavage site. Acn stability also was regulated by AKT1-mediated phosphorylation. Flies that expressed stabilized forms of Acn, either the phosphomimetic Acn(S641,731D) or the caspase-resistant Acn(D527A), exhibited enhanced basal autophagy. Physiologically, these flies showed improvements in processes known to be autophagy dependent, including increased starvation resistance, reduced Huntingtin-induced neurodegeneration, and prolonged life span. These data indicate that AKT1 and caspase-dependent regulation of Acn stability adjusts basal autophagy levels.

Indexed as

AutophagyAmino Acid SequenceAnimalsApoptosisBinding SitesCaspasesConserved SequenceDrosophila melanogasterDrosophila ProteinsGene Expression RegulationLongevityMolecular Sequence DataMutationProtein StabilityProto-Oncogene Proteins c-aktSequence AlignmentAcn protein, DrosophilaAkt1 protein, DrosophilaCaspasesDcp-1 protein, DrosophilaDrosophila ProteinsProto-Oncogene Proteins c-aktTranscription Factors

Identifiers

PMID25332163
PMCPMC4210446
OpenAlexW2104345850

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.