Evidence map›Paper›PMID 31353312›Full record

ArticleDevelopmental cell2019

AAGAB Controls AP2 Adaptor Assembly in Clathrin-Mediated Endocytosis.

Daniel R Gulbranson, Lauren Crisman, MyeongSeon Lee, Yan Ouyang, Bridget L Menasche, Brittany A Demmitt, Chun Wan, Toshifumi Nomura, Yihong Ye, Haijia Yu and 1 more

Abstract read
In one paragraph

Article in Developmental cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

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

  1. Pooled it
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  5. Review
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  13. Stepwise assembly of the AP2 endocytic clathrin adaptor complex.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. An AAGAB-to-CCDC32 handover mechanism controls the assembly of the AP2 adaptor complex.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. 5-HTInternational journal of molecular sciences · 2023
    Article
  16. Article
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  19. Article
  20. Oligomer-to-monomer transition underlies the chaperone function of AAGAB in AP1/AP2 assembly.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

11 authors.

Daniel R GulbransonDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Lauren CrismanDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
MyeongSeon LeeDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Yan OuyangDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Bridget L MenascheDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Brittany A DemmittDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA; Institute for Behavioral Genetics, University of Colorado, Boulder, CO 80309, USA.
Chun WanDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Toshifumi NomuraDepartment of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Yihong YeLaboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Haijia YuDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA; Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing 210023, China. Electronic address: haijiayu@gmail.com.
Jingshi ShenDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA. Electronic address: jingshi.shen@colorado.edu.

Funding

Roles of protein misfolding in neurodegenerative diseasesZIADK075145 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI YE, YIHONG · 2017 to 2025
$6.6M
TRAINING IN SIGNAL TRANSDUCTION &CELL CYCLE REGULATIONT32GM008759 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI AHN, NATALIE G. · 2000 to 2020
$5.9M
Predoctoral Training Program in Signaling and Cellular Regulation INCLUDE Down Syndrome SupplementT32GM142607 · NIGMS · UNIVERSITY OF COLORADO · PI Sabrina Leigh Spencer, Tin Tin Su · 2021 to 2026
$3.6M
Protein-membrane interactions in regulated exocytosisR35GM126960 · NIGMS · UNIVERSITY OF COLORADO · PI Jingshi Shen · 2018 to 2026
$3.2M
Identifying exosome-mediated cargo transport machinery in Alzheimer's diseaseRF1AG061829 · NIA · UNIVERSITY OF COLORADO · PI SHEN, JINGSHI, STOWELL, MICHAEL H. B. · 2018 to 2018
$2.7M
Regulatory Mechanisms of GLUT4 ExocytosisR01DK095367 · NIDDK · UNIVERSITY OF COLORADO · PI SHEN, JINGSHI · 2013 to 2017
$1.7M
Mechanisms of GLUT4 ExocytosisR01DK124431 · NIDDK · UNIVERSITY OF COLORADO · PI SHEN, JINGSHI · 2020 to 2022
$1.1M
Regulatory Mechanisms of GLUT4 ExocytosisR56DK095367 · NIDDK · UNIVERSITY OF COLORADO · PI SHEN, JINGSHI · 2012 to 2018
$598k
NIA NIH HHS RF1 AG061829NIDDK NIH HHS R01 DK095367NIDDK NIH HHS R01 DK124431NIDDK NIH HHS R56 DK095367NIGMS NIH HHS R35 GM126960NIGMS NIH HHS T32 GM008759NIGMS NIH HHS T32 GM142607
6 · The paper itself

Abstract

Multimeric adaptors are broadly involved in vesicle-mediated membrane trafficking. AP2 adaptor, in particular, plays a central role in clathrin-mediated endocytosis (CME) by recruiting cargo and clathrin to endocytic sites. It is generally thought that trafficking adaptors such as AP2 adaptor assemble spontaneously. In this work, however, we discovered that AP2 adaptor assembly is an ordered process controlled by alpha and gamma adaptin binding protein (AAGAB), an uncharacterized factor identified in our genome-wide genetic screen of CME. AAGAB guides the sequential association of AP2 subunits and stabilizes assembly intermediates. Without the assistance of AAGAB, AP2 subunits fail to form the adaptor complex, leading to their degradation. The function of AAGAB is abrogated by a mutation that causes punctate palmoplantar keratoderma type 1 (PPKP1), a human skin disease. Since other multimeric trafficking adaptors operate in an analogous manner to AP2 adaptor, their assembly likely involves a similar regulatory mechanism.

Indexed as

Adaptor Protein Complex 2Adaptor Proteins, Vesicular TransportAmino Acid SequenceCell MembraneClathrinEndocytosisHumansKeratoderma, PalmoplantarProtein BindingProtein TransportProteolysisAAGAB protein, humanAdaptor Protein Complex 2Adaptor Proteins, Vesicular TransportClathrinadaptor complexAP1 adaptorAP2 adaptorclathrin-mediated endocytosisCRISPR screenmembrane trafficking

Identifiers

PMID31353312
PMCPMC6702059

What OpenQuestion holds

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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.