Evidence map›Paper›PMID 38849673›Full record

ArticleEMBO reports2024

DLG1 functions upstream of SDCCAG3 and IFT20 to control ciliary targeting of polycystin-2.

Csenge K Rezi, Mariam G Aslanyan, Gaurav D Diwan, Tao Cheng, Mohamed Chamlali, Katrin Junger, Zeinab Anvarian, Esben Lorentzen, Kleo B Pauly, Yasmin Afshar-Bahadori and 12 more

Abstract read
In one paragraph

Article in EMBO reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Csenge K ReziDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID 0009-0005-5192-0151
Mariam G AslanyanDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.
Gaurav D DiwanBioQuant, Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-3928-3020
Tao ChengDepartment of Medicine (Nephrology Division) and Department of Cell Biology and Physiology, Washington University, St Louis, MO, USA.
Mohamed ChamlaliDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-9942-1424
Katrin JungerInstitute for Ophthalmic Research, Eberhard Karl University of Tübingen, Tübingen, Germany.ORCID 0000-0001-9681-2908
Zeinab AnvarianDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Esben LorentzenDepartment of Molecular Biology and Genetics - Protein Science, Aarhus University, Aarhus, Denmark.ORCID 0000-0001-6493-7220
Kleo B PaulyDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Yasmin Afshar-BahadoriDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Eduardo Fa FernandesCenter for Biopharmaceuticals, Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Feng QianDivision of Nephrology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID 0000-0001-9595-9772
Sébastien TosiDanish BioImaging Infrastructure Image Analysis Core Facility (DBI-INFRA IACF), University of Copenhagen, Copenhagen, Denmark.
Søren T ChristensenDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0001-5004-304X
Stine F PedersenDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-3044-7714
Kristian StrømgaardCenter for Biopharmaceuticals, Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Robert B RussellBioQuant, Heidelberg University, Heidelberg, Germany.ORCID 0000-0002-1905-4717
Jeffrey H MinerDepartment of Medicine (Nephrology Division) and Department of Cell Biology and Physiology, Washington University, St Louis, MO, USA.
Moe R MahjoubDepartment of Medicine (Nephrology Division) and Department of Cell Biology and Physiology, Washington University, St Louis, MO, USA.ORCID 0000-0001-8129-7464
Karsten BoldtInstitute for Ophthalmic Research, Eberhard Karl University of Tübingen, Tübingen, Germany.
Ronald RoepmanDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-5178-8163
Lotte B PedersenDepartment of Biology, University of Copenhagen, Copenhagen, Denmark. lbpedersen@bio.ku.dk.ORCID 0000-0002-9749-3758

Funding

PKD Innovation and Resource Development CoreU54DK126114 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI Terry J Watnick · 2020 to 2026
$7.3M
CENTROSOME DYSFUNCTION IN POLYCYSTIC KIDNEY DISEASER01DK108005 · NIDDK · WASHINGTON UNIVERSITY · PI MAHJOUB, MOHAMED REZA · 2016 to 2020
$1.7M
Danmarks Frie Forskningsfond (DFF) 2032-00115BDanmarks Frie Forskningsfond (DFF) 3103-00177BDutch Kidney Foundation 20OI174European Union's Horizon 2020 research and innovation program Marie Sklodowska-Curie Innovative Training Networks 861329NIDDK NIH HHS R01 DK108005NIDDK NIH HHS R01-DK108005NIDDK NIH HHS U54 DK126114Novo Nordisk Fonden (NNF) NNF18SA0032928Novo Nordisk Fonden (NNF) NNF22OC0080406PKD RRC U54DK126114Wellcome TrustWellcome Trust (WT) 201585/B/18/Z
6 · The paper itself

Abstract

Polarized vesicular trafficking directs specific receptors and ion channels to cilia, but the underlying mechanisms are poorly understood. Here we describe a role for DLG1, a core component of the Scribble polarity complex, in regulating ciliary protein trafficking in kidney epithelial cells. Conditional knockout of Dlg1 in mouse kidney causes ciliary elongation and cystogenesis, and cell-based proximity labeling proteomics and fluorescence microscopy show alterations in the ciliary proteome upon loss of DLG1. Specifically, the retromer-associated protein SDCCAG3, IFT20, and polycystin-2 (PC2) are reduced in the cilia of DLG1-deficient cells compared to control cells. This phenotype is recapitulated in vivo and rescuable by re-expression of wild-type DLG1, but not a Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)-associated DLG1 variant, p.T489R. Finally, biochemical approaches and Alpha Fold modelling suggest that SDCCAG3 and IFT20 form a complex that associates, at least indirectly, with DLG1. Our work identifies a key role for DLG1 in regulating ciliary protein composition and suggests that ciliary dysfunction of the p.T489R DLG1 variant may contribute to CAKUT.

Indexed as

Carrier ProteinsCiliaDiscs Large Homolog 1 ProteinTRPP Cation ChannelsAnimalsEpithelial CellsHumansKidneyMembrane ProteinsMiceMice, KnockoutProtein BindingProtein TransportUrogenital AbnormalitiesVesico-Ureteral RefluxCarrier ProteinsDiscs Large Homolog 1 ProteinDlg1 protein, mouseIft20 protein, mouseMembrane ProteinsTRPP Cation ChannelsDLG1IFT20Polycystin-2Primary CiliaSDCCAG3

Identifiers

PMID38849673
PMCPMC11239879

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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.