Evidence map›Paper›PMID 27666370›Full record

ArticleAmerican journal of human genetics2016

Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy.

Elisabetta Flex, Marcello Niceta, Serena Cecchetti, Isabelle Thiffault, Margaret G Au, Alessandro Capuano, Emanuela Piermarini, Anna A Ivanova, Joshua W Francis, Giovanni Chillemi and 21 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 79 citations in OpenAlex.

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  11. Novel Compound Heterozygous Variants inChildren (Basel, Switzerland) · 2021
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  18. A Novel CCT5 Missense Variant Associated with Early Onset Motor Neuropathy.International journal of molecular sciences · 2020
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  19. Review
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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

31 authors at 11 institutions in 3 countries.

Elisabetta FlexDepartment of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome 00161, Italy.
Marcello NicetaGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Serena CecchettiDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome 00161, Italy.
Isabelle ThiffaultCenter for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA; University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA.
Margaret G AuDepartment of Pediatrics, Medical Genetics, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Alessandro CapuanoGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Emanuela PiermariniGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Anna A IvanovaDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.
Joshua W FrancisDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.
Giovanni ChillemiCINECA, SCAI-SuperComputing Applications and Innovation Department, Rome 00185, Italy.
Balasubramanian ChandramouliScuola Normale Superiore, 56126 Pisa, Italy.
Giovanna CarpentieriDepartment of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome 00161, Italy; Dipartimento di Medicina Sperimentale, Sapienza Università di Roma, Rome 00161, Italy.
Charlotte A HaaxmaDepartment of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen 1105, the Netherlands.
Andrea CiolfiGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy; Centro di Ricerca per gli alimenti e la nutrizione, CREA, Rome 00178, Italy.
Simone PizziGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Ganka V DouglasGeneDx, Gaithersburg, MD 20877, USA.
Kara LevineGeneDx, Gaithersburg, MD 20877, USA.
Antonella SferraGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Maria Lisa DenticiGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Rolph R PfundtDepartment of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen 1105, the Netherlands.
Jean-Baptiste Le PichonDepartment of Pediatrics, Children's Mercy Hospitals, Kansas City, MO 64108, USA.
Emily FarrowCenter for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA.
Frank BaasDepartment of Genome Analysis, Academic Medical Center, Amsterdam 1105, the Netherlands.
Fiorella PiemonteGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Bruno DallapiccolaGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
John M GrahamDepartment of Pediatrics, Medical Genetics, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Carol J SaundersCenter for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, MO 64108, USA; University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA.
Enrico BertiniGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy.
Richard A KahnDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, USA.
David A KoolenDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen 1105, the Netherlands.
Marco TartagliaGenetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Rome 00146, Italy. Electronic address: marco.tartaglia@opbg.net.
Bambino Gesù Children's Hospital · ITEmory University · USIstituto Superiore di Sanità · ITCedars-Sinai Medical Center · USChildren's Mercy Hospital · USRadboud University Medical Center · NLUniversity of Missouri–Kansas City · USAcademic Medical Center · NLCineca · ITRadboud University Nijmegen · NLScuola Normale Superiore · IT

Funding

Molecular mechanisms of ARF family GTPasesR35GM122568 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2017 to 2024
$3.7M
The Regulation and Cellular Activities of the ARL2 GTPaseR01GM090158 · NIGMS · EMORY UNIVERSITY · PI KAHN, RICHARD A · 2010 to 2017
$2.5M
A Novel Mechanism of GTPase Regulation: Arl2 Interaction with TBCDF31CA189672 · NCI · EMORY UNIVERSITY · PI FRANCIS, JOSHUA W · 2014 to 2016
$126k
NCI NIH HHS F31 CA189672NIGMS NIH HHS R01 GM090158NIGMS NIH HHS R35 GM122568
6 · The paper itself

Abstract

Microtubules are dynamic cytoskeletal elements coordinating and supporting a variety of neuronal processes, including cell division, migration, polarity, intracellular trafficking, and signal transduction. Mutations in genes encoding tubulins and microtubule-associated proteins are known to cause neurodevelopmental and neurodegenerative disorders. Growing evidence suggests that altered microtubule dynamics may also underlie or contribute to neurodevelopmental disorders and neurodegeneration. We report that biallelic mutations in TBCD, encoding one of the five co-chaperones required for assembly and disassembly of the αβ-tubulin heterodimer, the structural unit of microtubules, cause a disease with neurodevelopmental and neurodegenerative features characterized by early-onset cortical atrophy, secondary hypomyelination, microcephaly, thin corpus callosum, developmental delay, intellectual disability, seizures, optic atrophy, and spastic quadriplegia. Molecular dynamics simulations predicted long-range and/or local structural perturbations associated with the disease-causing mutations. Biochemical analyses documented variably reduced levels of TBCD, indicating relative instability of mutant proteins, and defective β-tubulin binding in a subset of the tested mutants. Reduced or defective TBCD function resulted in decreased soluble α/β-tubulin levels and accelerated microtubule polymerization in fibroblasts from affected subjects, demonstrating an overall shift toward a more rapidly growing and stable microtubule population. These cells displayed an aberrant mitotic spindle with disorganized, tangle-shaped microtubules and reduced aster formation, which however did not alter appreciably the rate of cell proliferation. Our findings establish that defective TBCD function underlies a recognizable encephalopathy and drives accelerated microtubule polymerization and enhanced microtubule stability, underscoring an additional cause of altered microtubule dynamics with impact on neuronal function and survival in the developing brain.

Indexed as

AllelesMutationProtein FoldingAdolescentAge of OnsetBrainBrain DiseasesCell ProliferationChild, PreschoolFemaleFibroblastsHumansInfantMaleMicrotubule-Associated ProteinsMicrotubulesMicrotubule-Associated ProteinsMolecular ChaperonesTBCD protein, humanTubulin

Identifiers

PMID27666370
PMCPMC5065658
OpenAlexW2522950450

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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.