Literature DB >> 27666370

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

Elisabetta Flex1, Marcello Niceta2, Serena Cecchetti3, Isabelle Thiffault4, Margaret G Au5, Alessandro Capuano2, Emanuela Piermarini2, Anna A Ivanova6, Joshua W Francis6, Giovanni Chillemi7, Balasubramanian Chandramouli8, Giovanna Carpentieri9, Charlotte A Haaxma10, Andrea Ciolfi11, Simone Pizzi2, Ganka V Douglas12, Kara Levine12, Antonella Sferra2, Maria Lisa Dentici2, Rolph R Pfundt10, Jean-Baptiste Le Pichon13, Emily Farrow14, Frank Baas15, Fiorella Piemonte2, Bruno Dallapiccola2, John M Graham5, Carol J Saunders4, Enrico Bertini2, Richard A Kahn6, David A Koolen16, Marco Tartaglia17.   

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.
Copyright © 2016 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27666370      PMCID: PMC5065658          DOI: 10.1016/j.ajhg.2016.08.003

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  64 in total

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Journal:  Hum Mutat       Date:  2013-10-18       Impact factor: 4.878

2.  Parkin mutations reduce the complexity of neuronal processes in iPSC-derived human neurons.

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Authors:  J Hazan; N Fonknechten; D Mavel; C Paternotte; D Samson; F Artiguenave; C S Davoine; C Cruaud; A Dürr; P Wincker; P Brottier; L Cattolico; V Barbe; J M Burgunder; J F Prud'homme; A Brice; B Fontaine; B Heilig; J Weissenbach
Journal:  Nat Genet       Date:  1999-11       Impact factor: 38.330

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Journal:  Nat Genet       Date:  2002-10-21       Impact factor: 38.330

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Authors:  L Martín; M L Fanarraga; K Aloria; J C Zabala
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7.  Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.

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Journal:  Sci Transl Med       Date:  2014-12-03       Impact factor: 17.956

8.  Effect of TBCD and its regulatory interactor Arl2 on tubulin and microtubule integrity.

Authors:  Guoling Tian; Simi Thomas; Nicholas J Cowan
Journal:  Cytoskeleton (Hoboken)       Date:  2010-11

9.  dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations.

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10.  Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

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Journal:  Brain       Date:  2010-10-15       Impact factor: 15.255

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  28 in total

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Authors:  Valentina Muto; Elisabetta Flex; Zachary Kupchinsky; Guido Primiano; Hamid Galehdari; Mohammadreza Dehghani; Serena Cecchetti; Giovanna Carpentieri; Teresa Rizza; Neda Mazaheri; Alireza Sedaghat; Mohammad Yahya Vahidi Mehrjardi; Alice Traversa; Michela Di Nottia; Maria M Kousi; Yalda Jamshidi; Andrea Ciolfi; Viviana Caputo; Reza Azizi Malamiri; Francesca Pantaleoni; Simone Martinelli; Aaron R Jeffries; Jawaher Zeighami; Amir Sherafat; Daniela Di Giuda; Gholam Reza Shariati; Rosalba Carrozzo; Nicholas Katsanis; Reza Maroofian; Serenella Servidei; Marco Tartaglia
Journal:  Neurology       Date:  2018-06-29       Impact factor: 9.910

2.  Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.

Authors:  Elisabetta Flex; Simone Martinelli; Anke Van Dijck; Andrea Ciolfi; Serena Cecchetti; Elisa Coluzzi; Luca Pannone; Cristina Andreoli; Francesca Clementina Radio; Simone Pizzi; Giovanna Carpentieri; Alessandro Bruselles; Giuseppina Catanzaro; Lucia Pedace; Evelina Miele; Elena Carcarino; Xiaoyan Ge; Chieko Chijiwa; M E Suzanne Lewis; Marije Meuwissen; Sandra Kenis; Nathalie Van der Aa; Austin Larson; Kathleen Brown; Melissa P Wasserstein; Brian G Skotko; Amber Begtrup; Richard Person; Maria Karayiorgou; J Louw Roos; Koen L Van Gassen; Marije Koopmans; Emilia K Bijlsma; Gijs W E Santen; Daniela Q C M Barge-Schaapveld; Claudia A L Ruivenkamp; Mariette J V Hoffer; Seema R Lalani; Haley Streff; William J Craigen; Brett H Graham; Annette P M van den Elzen; Daan J Kamphuis; Katrin Õunap; Karit Reinson; Sander Pajusalu; Monica H Wojcik; Clara Viberti; Cornelia Di Gaetano; Enrico Bertini; Simona Petrucci; Alessandro De Luca; Rossella Rota; Elisabetta Ferretti; Giuseppe Matullo; Bruno Dallapiccola; Antonella Sgura; Magdalena Walkiewicz; R Frank Kooy; Marco Tartaglia
Journal:  Am J Hum Genet       Date:  2019-08-22       Impact factor: 11.025

3.  A Faroese founder variant in TBCD causes early onset, progressive encephalopathy with a homogenous clinical course.

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Journal:  Eur J Hum Genet       Date:  2018-06-19       Impact factor: 4.246

4.  A Trimer Consisting of the Tubulin-specific Chaperone D (TBCD), Regulatory GTPase ARL2, and β-Tubulin Is Required for Maintaining the Microtubule Network.

Authors:  Joshua W Francis; Laura E Newman; Leslie A Cunningham; Richard A Kahn
Journal:  J Biol Chem       Date:  2017-01-26       Impact factor: 5.157

5.  Biallelic pathogenic variants in TBCD-related neurodevelopment disease with mild clinical features.

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Journal:  Neurol Sci       Date:  2019-06-25       Impact factor: 3.307

6.  Daily Outpatient Physical Therapy for a Toddler With a Neurodegenerative Disease: A Case Report.

Authors:  Rachel Bican; Rachel Ferrante; Sarah Hendershot; Michelle Byars; Warren Lo; Jill C Heathcock
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7.  "Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia.

Authors:  B Pascual; S T de Bot; M R Daniels; M C França; C Toro; M Riverol; P Hedera; M T Bassi; N Bresolin; B P van de Warrenburg; B Kremer; J Nicolai; P Charles; J Xu; S Singh; N J Patronas; S H Fung; M D Gregory; J C Masdeu
Journal:  AJNR Am J Neuroradiol       Date:  2019-01-03       Impact factor: 3.825

8.  Nucleotide Binding to ARL2 in the TBCD∙ARL2∙β-Tubulin Complex Drives Conformational Changes in β-Tubulin.

Authors:  Joshua W Francis; Devrishi Goswami; Scott J Novick; Bruce D Pascal; Emily R Weikum; Eric A Ortlund; Patrick R Griffin; Richard A Kahn
Journal:  J Mol Biol       Date:  2017-09-29       Impact factor: 5.469

9.  Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome.

Authors:  Christiane K Bauer; Paolo Calligari; Francesca Clementina Radio; Viviana Caputo; Maria Lisa Dentici; Nadia Falah; Frances High; Francesca Pantaleoni; Sabina Barresi; Andrea Ciolfi; Simone Pizzi; Alessandro Bruselles; Richard Person; Sarah Richards; Megan T Cho; Daniela J Claps Sepulveda; Stefano Pro; Roberta Battini; Giuseppe Zampino; Maria Cristina Digilio; Gianfranco Bocchinfuso; Bruno Dallapiccola; Lorenzo Stella; Marco Tartaglia
Journal:  Am J Hum Genet       Date:  2018-10-04       Impact factor: 11.025

10.  A mild form of adenylosuccinate lyase deficiency in absence of typical brain MRI features diagnosed by whole exome sequencing.

Authors:  Marina Macchiaiolo; Sabina Barresi; Francesco Cecconi; Ginevra Zanni; Marcello Niceta; Emanuele Bellacchio; Giacomo Lazzarino; Angela Maria Amorini; Enrico Silvio Bertini; Salvatore Rizza; Benedetta Contardi; Marco Tartaglia; Andrea Bartuli
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