Evidence map›Paper›PMID 31794024›Full record

ArticleBrain : a journal of neurology2020

Deficiencies in vesicular transport mediated by TRAPPC4 are associated with severe syndromic intellectual disability.

Nicole J Van Bergen, Yiran Guo, Noraldin Al-Deri, Zhanna Lipatova, Daniela Stanga, Sarah Zhao, Rakhilya Murtazina, Valeriya Gyurkovska, Davut Pehlivan, Tadahiro Mitani and 23 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 9% 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, 46 citations in OpenAlex.

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  17. Newer Methods Drive Recent Insights into Rab GTPase Biology: An Overview.Methods in molecular biology (Clifton, N.J.) · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors at 11 institutions in 4 countries.

Nicole J Van BergenBrain and Mitochondrial Research Group, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.
Yiran GuoCenter for Applied Genomics (CAG) at the Children's Hospital of Philadelphia (CHOP), Philadelphia, USA.
Noraldin Al-DeriDepartment of Biology, Concordia University, Montreal, Quebec, Canada.
Zhanna LipatovaDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Daniela StangaDepartment of Biology, Concordia University, Montreal, Quebec, Canada.
Sarah ZhaoDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Rakhilya MurtazinaDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Valeriya GyurkovskaDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Davut PehlivanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Tadahiro MitaniDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Alper GezdiriciDepartment of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, 34303, Turkey.
Jayne AntonyTY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Sydney, Australia.
Felicity CollinsWestern Sydney Genetics Program, Children's Hospital at Westmead, Sydney, Australia.
Mary J H WillisDepartment of Pediatrics, Naval Medical Center San Diego, San Diego, California, USA.
Zeynep H Coban AkdemirDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Pengfei LiuDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Jaya PunethaDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Jill V HunterDepartment of Radiology, Baylor College of Medicine, Houston, Texas, 77030, USA.
Shalini N JhangianiHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Jawid M FatihDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Jill A RosenfeldDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Jennifer E PoseyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Richard A GibbsDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Ender KaracaDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Sean MasseyBrain and Mitochondrial Research Group, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.
Thisara G RanasingheBrain and Mitochondrial Research Group, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.
Patrick SleimanCenter for Applied Genomics (CAG) at the Children's Hospital of Philadelphia (CHOP), Philadelphia, USA.
Chris TroedsonTY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Sydney, Australia.
James R LupskiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, 77030, USA.
Michael SacherDepartment of Biology, Concordia University, Montreal, Quebec, Canada.
Nava SegevDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago, Chicago, IL, USA.
Hakon HakonarsonCenter for Applied Genomics (CAG) at the Children's Hospital of Philadelphia (CHOP), Philadelphia, USA.
John ChristodoulouBrain and Mitochondrial Research Group, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.
Baylor College of Medicine · USUniversity of Illinois Chicago · USRoyal Children's Hospital · AUChildren's Hospital of Philadelphia · USChildren's Hospital at Westmead · AUConcordia University · CAİstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi · TRMcGill University · CANaval Medical Center San Diego · USRoyal Prince Alfred Hospital · AUUniversity of Alabama at Birmingham · US

Funding

Baylor-Johns Hopkins Center for Mendelian GeneticsU54HG006542 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 2012 to 2015
$15.6M
Baylor-Johns Hopkins Center for Mendelian GeneticsUM1HG006542 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 2016 to 2020
$14.5M
YPTL GTPASE AND VESICULAR TRANSPORTR01GM045444 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SEGEV, NAVA · 1992 to 2020
$6.4M
STRUCTURAL VARIATION IN NEUROLOGICAL DISEASER35NS105078 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI LUPSKI, JAMES R. · 2018 to 2025
$6.0M
Coordination of intracellular trafficking pathways by Ypt/Rab GTPases and their GEFs.R35GM141479 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SEGEV, NAVA · 2021 to 2025
$2.4M
The role of Rab1 GTPase and its activators in selective autophagy and neurodegenerative diseaseR21NS099556 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SEGEV, NAVA · 2016 to 2017
$400k
NHGRI NIH HHS U54 HG006542NHGRI NIH HHS UM1 HG006542NIGMS NIH HHS R01 GM045444NIGMS NIH HHS R35 GM141479NINDS NIH HHS R21 NS099556NINDS NIH HHS R35 NS105078
6 · The paper itself

Abstract

The conserved transport protein particle (TRAPP) complexes regulate key trafficking events and are required for autophagy. TRAPPC4, like its yeast Trs23 orthologue, is a core component of the TRAPP complexes and one of the essential subunits for guanine nucleotide exchange factor activity for Rab1 GTPase. Pathogenic variants in specific TRAPP subunits are associated with neurological disorders. We undertook exome sequencing in three unrelated families of Caucasian, Turkish and French-Canadian ethnicities with seven affected children that showed features of early-onset seizures, developmental delay, microcephaly, sensorineural deafness, spastic quadriparesis and progressive cortical and cerebellar atrophy in an effort to determine the genetic aetiology underlying neurodevelopmental disorders. All seven affected subjects shared the same identical rare, homozygous, potentially pathogenic variant in a non-canonical, well-conserved splice site within TRAPPC4 (hg19:chr11:g.118890966A>G; TRAPPC4: NM_016146.5; c.454+3A>G). Single nucleotide polymorphism array analysis revealed there was no haplotype shared between the tested Turkish and Caucasian families suggestive of a variant hotspot region rather than a founder effect. In silico analysis predicted the variant to cause aberrant splicing. Consistent with this, experimental evidence showed both a reduction in full-length transcript levels and an increase in levels of a shorter transcript missing exon 3, suggestive of an incompletely penetrant splice defect. TRAPPC4 protein levels were significantly reduced whilst levels of other TRAPP complex subunits remained unaffected. Native polyacrylamide gel electrophoresis and size exclusion chromatography demonstrated a defect in TRAPP complex assembly and/or stability. Intracellular trafficking through the Golgi using the marker protein VSVG-GFP-ts045 demonstrated significantly delayed entry into and exit from the Golgi in fibroblasts derived from one of the affected subjects. Lentiviral expression of wild-type TRAPPC4 in these fibroblasts restored trafficking, suggesting that the trafficking defect was due to reduced TRAPPC4 levels. Consistent with the recent association of the TRAPP complex with autophagy, we found that the fibroblasts had a basal autophagy defect and a delay in autophagic flux, possibly due to unsealed autophagosomes. These results were validated using a yeast trs23 temperature sensitive variant that exhibits constitutive and stress-induced autophagic defects at permissive temperature and a secretory defect at restrictive temperature. In summary we provide strong evidence for pathogenicity of this variant in a member of the core TRAPP subunit, TRAPPC4 that associates with vesicular trafficking and autophagy defects. This is the first report of a TRAPPC4 variant, and our findings add to the growing number of TRAPP-associated neurological disorders.

Indexed as

AtrophyAutophagyCerebellumCerebral CortexChildChild, PreschoolCraniofacial AbnormalitiesDeafnessDevelopmental DisabilitiesEpilepsyFemaleFibroblastsHearing Loss, SensorineuralHumansInfantInfant, NewbornNerve Tissue ProteinsRNA Splice SitesTRAPPC4 protein, humanVesicular Transport Proteinsautophagyintellectual disabilitymolecular geneticsvesicular transportwhole-exome sequencing

Identifiers

PMID31794024
PMCPMC6935753
OpenAlexW2993619711

What OpenQuestion holds

Textmetadata
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.