Literature DB >> 24243101

Microtubules and neurodevelopmental disease: the movers and the makers.

Martin Breuss1, David A Keays.   

Abstract

The development of the mammalian cortex requires the generation, migration and differentiation of neurons. Each of these cellular events requires a dynamic microtubule cytoskeleton. Microtubules are required for interkinetic nuclear migration, the separation of chromatids in mitosis, nuclear translocation during migration and the outgrowth of neurites. Their importance is underlined by the finding that mutations in a host of microtubule associated proteins cause detrimental neurological disorders. More recently, the structural subunits of microtubules, the tubulin proteins, have been implicated in a spectrum of human diseases collectively known as the tubulinopathies. This chapter reviews the discovery of microtubules, the role they play in neurodevelopment, and catalogues the tubulin isoforms associated with neurodevelopmental disease. Our focus is on the molecular and cellular mechanisms that underlie the pathology of tubulin-associated diseases. Finally, we reflect on whether different tubulin genes have distinct intrinsic functions.

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Year:  2014        PMID: 24243101     DOI: 10.1007/978-94-007-7687-6_5

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  20 in total

1.  Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

Authors:  Mala Isrie; Martin Breuss; Guoling Tian; Andi Harley Hansen; Francesca Cristofoli; Jasmin Morandell; Zachari A Kupchinsky; Alejandro Sifrim; Celia Maria Rodriguez-Rodriguez; Elena Porta Dapena; Kurston Doonanco; Norma Leonard; Faten Tinsa; Stéphanie Moortgat; Hakan Ulucan; Erkan Koparir; Ender Karaca; Nicholas Katsanis; Valeria Marton; Joris Robert Vermeesch; Erica E Davis; Nicholas J Cowan; David Anthony Keays; Hilde Van Esch
Journal:  Am J Hum Genet       Date:  2015-12-03       Impact factor: 11.025

2.  De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders.

Authors:  Marija Dulovic-Mahlow; Joanne Trinh; Krishna Kumar Kandaswamy; Geir Julius Braathen; Nataliya Di Donato; Elisa Rahikkala; Skadi Beblo; Martin Werber; Victor Krajka; Øyvind L Busk; Hauke Baumann; Nouriya Abbas Al-Sannaa; Frauke Hinrichs; Rabea Affan; Nir Navot; Mohammed A Al Balwi; Gabriela Oprea; Øystein L Holla; Maximilian E R Weiss; Rami A Jamra; Anne-Karin Kahlert; Shivendra Kishore; Kristian Tveten; Melissa Vos; Arndt Rolfs; Katja Lohmann
Journal:  Am J Hum Genet       Date:  2019-06-20       Impact factor: 11.025

3.  Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway.

Authors:  Shimon Edvardson; Guoling Tian; Hayley Cullen; Hannah Vanyai; Linh Ngo; Saiuj Bhat; Adi Aran; Muhannad Daana; Naderah Da'amseh; Bassam Abu-Libdeh; Nicholas J Cowan; Julian Ik-Tsen Heng; Orly Elpeleg
Journal:  Hum Mol Genet       Date:  2016-11-01       Impact factor: 6.150

4.  Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos.

Authors:  Ruizhi Feng; Zheng Yan; Bin Li; Min Yu; Qing Sang; Guoling Tian; Yao Xu; Biaobang Chen; Ronggui Qu; Zhaogui Sun; Xiaoxi Sun; Li Jin; Lin He; Yanping Kuang; Nicholas J Cowan; Lei Wang
Journal:  J Med Genet       Date:  2016-06-06       Impact factor: 6.318

5.  Covalent binding of the organophosphate insecticide profenofos to tyrosine on α- and β-tubulin proteins.

Authors:  Shaogang Chu; Margaret R Baker; Gladys Leong; Robert J Letcher; Qing X Li
Journal:  Chemosphere       Date:  2018-02-20       Impact factor: 7.086

6.  Acquisition of Developmental Milestones in Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy.

Authors:  Francesco Gavazzi; Brittany A Charsar; Catherine Williams; Justine Shults; Cesar A Alves; Laura Adang; Adeline Vanderver
Journal:  J Child Neurol       Date:  2021-09       Impact factor: 2.363

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

Authors:  Elisabetta Flex; Marcello Niceta; Serena Cecchetti; Isabelle Thiffault; Margaret G Au; Alessandro Capuano; Emanuela Piermarini; Anna A Ivanova; Joshua W Francis; Giovanni Chillemi; Balasubramanian Chandramouli; Giovanna Carpentieri; Charlotte A Haaxma; Andrea Ciolfi; Simone Pizzi; Ganka V Douglas; Kara Levine; Antonella Sferra; Maria Lisa Dentici; Rolph R Pfundt; Jean-Baptiste Le Pichon; Emily Farrow; Frank Baas; Fiorella Piemonte; Bruno Dallapiccola; John M Graham; Carol J Saunders; Enrico Bertini; Richard A Kahn; David A Koolen; Marco Tartaglia
Journal:  Am J Hum Genet       Date:  2016-09-22       Impact factor: 11.025

8.  Aminochrome Toxicity is Mediated by Inhibition of Microtubules Polymerization Through the Formation of Adducts with Tubulin.

Authors:  Andrea Briceño; Patricia Muñoz; Patricia Brito; Sandro Huenchuguala; Juan Segura-Aguilar; Irmgard B Paris
Journal:  Neurotox Res       Date:  2015-09-07       Impact factor: 3.911

9.  Oleoylethanolamide Delays the Dysfunction and Death of Purkinje Cells and Ameliorates Behavioral Defects in a Mouse Model of Cerebellar Neurodegeneration.

Authors:  Ester Pérez-Martín; Rodrigo Muñoz-Castañeda; Marie-Jo Moutin; Carmelo A Ávila-Zarza; José M Muñoz-Castañeda; Carlos Del Pilar; José R Alonso; Annie Andrieux; David Díaz; Eduardo Weruaga
Journal:  Neurotherapeutics       Date:  2021-04-07       Impact factor: 6.088

Review 10.  Axonal mRNA translation in neurological disorders.

Authors:  Julie Qiaojin Lin; Francesca W van Tartwijk; Christine E Holt
Journal:  RNA Biol       Date:  2020-09-29       Impact factor: 4.652

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