Evidence map›Paper›PMID 33222586›Full record

ArticleAutophagy2021

GLIPR2 is a negative regulator of autophagy and the BECN1-ATG14-containing phosphatidylinositol 3-kinase complex.

Yuting Zhao, Zhongju Zou, Daxiao Sun, Yue Li, Sangita C Sinha, Li Yu, Lynda Bennett, Beth Levine

Open access · hybridAbstract read
In one paragraph

Article in Autophagy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  9. Cell Culture Differentiation and Proliferation Conditions Influence theAmerican journal of respiratory cell and molecular biology · 2024
    Article
  10. Article
  11. Neuronal autosis is NaCell death & disease · 2024
    Article
  12. Article
  13. CorticalProceedings of the National Academy of Sciences of the United States of America · 2024
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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

8 authors at 4 institutions in 2 countries.

Yuting ZhaoCenter for Autophagy Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-4332-6329
Zhongju ZouCenter for Autophagy Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-3937-5902
Daxiao SunThe State Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.
Yue LiDepartment of Chemistry and Biochemistry, North Dakota State University, Fargo, ND, USA.
Sangita C SinhaDepartment of Chemistry and Biochemistry, North Dakota State University, Fargo, ND, USA.ORCID 0000-0003-0953-4263
Li YuThe State Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.
Lynda BennettCenter for Autophagy Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-7491-5797
Beth LevineCenter for Autophagy Research, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-1460-1638
Howard Hughes Medical Institute · USNorth Dakota State University · USPeking University · CNThe University of Texas Southwestern Medical Center · US

Funding

RP5: Chemical proteomic discovery of small-molecule probes for autophagy proteinsU19AI142784 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI SHILOH, MICHAEL · 2019 to 2023
$36.9M
Genetic and Pathway Analysis CoreU19AI109725 · NIAID · WASHINGTON UNIVERSITY · PI VIRGIN, HERBERT W · 2014 to 2018
$32.7M
Elucidating the structural basis of differential interactions of human BECN paralogs and their role in cellular homeostasisR15GM122035 · NIGMS · NORTH DAKOTA STATE UNIVERSITY · PI SINHA, SANGITA · 2017 to 2017
$435k
NIAID NIH HHS U19 AI109725NIAID NIH HHS U19 AI142784NIGMS NIH HHS R15 GM122035
6 · The paper itself

Abstract

A key mediator of macroautophagy/autophagy induction is the class III phosphatidylinositol 3-kinase complex I (PtdIns3K-C1) consisting of PIK3C3/VPS34, PIK3R4/VPS15, BECN1, and ATG14. Although several proteins are known to enhance or decrease PtdIns3K-C1 activity, our understanding of the molecular regulation of PtdIns3K-C1 is still incomplete. Previously, we identified a Golgi-associated protein, GLIPR2, in a screen for proteins that interact with amino acids 267-284 of BECN1, a region of BECN1 sufficient to induce autophagy when fused to a cell penetrating leader sequence. In this study, we used CRISPR-Cas9-mediated depletion of GLIPR2 in cells and mice to investigate the role of GLIPR2 in the regulation of autophagy and PtdIns3K-C1 activity. Depletion of GLIPR2 in HeLa cells increased autelophagic flux and generation of phosphatidylinositol 3-phosphate (PtdIns3P).

Indexed as

AutophagyClass III Phosphatidylinositol 3-KinasesMembrane ProteinsAdaptor Proteins, Vesicular TransportAnimalsAutophagy-Related ProteinsBeclin-1HeLa CellsHumansMicePhosphorylationAdaptor Proteins, Vesicular TransportATG14 protein, humanAutophagy-Related ProteinsBeclin-1BECN1 protein, humanBecn1 protein, mouseClass III Phosphatidylinositol 3-KinasesGLIPR2 protein, humanMembrane ProteinsAutophagyBECN1GLIPR2GolgiPtdIns3k-C1 complexTat-BECN1 peptide

Identifiers

PMID33222586
PMCPMC8526008
OpenAlexW3109524898

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.