Evidence map›Paper›PMID 26553930›Full record

ArticleThe Journal of cell biology2015

Endosomal sorting of Notch receptors through COMMD9-dependent pathways modulates Notch signaling.

Haiying Li, Yeon Koo, Xicheng Mao, Luis Sifuentes-Dominguez, Lindsey L Morris, Da Jia, Naoteru Miyata, Rebecca A Faulkner, Jan M van Deursen, Marc Vooijs and 4 more

Open access · bronzeAbstract 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 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Structural basis for Retriever-SNX17 assembly and endosomal sorting.bioRxiv : the preprint server for biology · 2024
    Article
  13. Article
  14. Structural Organization of the Retriever-CCC Endosomal Recycling Complex.bioRxiv : the preprint server for biology · 2023
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Deliver on Time or Pay the Fine: Scheduling in Membrane Trafficking.International journal of molecular sciences · 2021
    Review
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

14 authors at 4 institutions in 2 countries.

Haiying LiDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Yeon KooDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Xicheng MaoDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Luis Sifuentes-DominguezDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Lindsey L MorrisDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Da JiaDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Naoteru MiyataDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Rebecca A FaulknerDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Jan M van DeursenDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905 Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905.
Marc VooijsDepartment of Radiotherapy (MAASTRO)/GROW-School for Developmental Biology and Oncology, Maastricht University, 6229 ER Maastricht, Netherlands.
Daniel D BilladeauDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905 Department of Immunology, Mayo Clinic, Rochester, MN 55905.
Bart van de SluisMolecular Genetics Section - Department of Pediatrics, University of Groningen, University Medical Center Groningen, 9713 AV Groningen, Netherlands.
Ondine CleaverDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Ezra BursteinDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390 Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390 ezra.burstein@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · USMayo Clinic · USMaastricht University · NLUniversity Medical Center Groningen · NL

Funding

UT GASTROENTEROLOGY/HEPATOLOGY RESEARCH TRAINING PROGRAMT32DK007745 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Rodney E Infante · 1997 to 2026
$6.8M
Role of the CCC complex in immune functionR01DK073639 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BURSTEIN, EZRA · 2007 to 2020
$3.7M
Regulation of Actin Dynamics During T Cell ActivationR01AI065474 · NIAID · MAYO CLINIC ROCHESTER · PI BILLADEAU, DANIEL D · 2005 to 2014
$3.1M
NF-kB Signaling Insights from a Rare X-linked Immunodeficiency SyndromeR56AI113274 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI BURSTEIN, EZRA, ZINN, ANDREW R. · 2014 to 2014
$398k
NIAID NIH HHS AI065474NIAID NIH HHS R01 AI065474NIAID NIH HHS R56 AI113274NIAID NIH HHS R56AI113274NIDDK NIH HHS R01 DK073639NIDDK NIH HHS R01DK073639NIDDK NIH HHS T32 DK007745
6 · The paper itself

Abstract

Notch family members are transmembrane receptors that mediate essential developmental programs. Upon ligand binding, a proteolytic event releases the intracellular domain of Notch, which translocates to the nucleus to regulate gene transcription. In addition, Notch trafficking across the endolysosomal system is critical in its regulation. In this study we report that Notch recycling to the cell surface is dependent on the COMMD-CCDC22-CCDC93 (CCC) complex, a recently identified regulator of endosomal trafficking. Disruption in this system leads to intracellular accumulation of Notch2 and concomitant reduction in Notch signaling. Interestingly, among the 10 copper metabolism MURR1 domain containing (COMMD) family members that can associate with the CCC complex, only COMMD9 and its binding partner, COMMD5, have substantial effects on Notch. Furthermore, Commd9 deletion in mice leads to embryonic lethality and complex cardiovascular alterations that bear hallmarks of Notch deficiency. Altogether, these studies highlight that the CCC complex controls Notch activation by modulating its intracellular trafficking and demonstrate cargo-specific effects for members of the COMMD protein family.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell LineCell Line, TumorCell MembraneCell NucleusEndosomesHEK293 CellsHeLa CellsHumansMiceProtein TransportReceptors, NotchSignal TransductionAdaptor Proteins, Signal TransducingCarrier ProteinsReceptors, Notch

Identifiers

PMID26553930
PMCPMC4639872
OpenAlexW2101720625

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.