Literature DB >> 10828619

Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35.

M van Geel1, J C van Deutekom, A van Staalduinen, R J Lemmers, M C Dickson, M H Hofker, G W Padberg, J E Hewitt, P J de Jong, R R Frants.   

Abstract

The human beta-tubulin supergene family consists of several isotypes with many associated pseudogenes. Here we report the identification of yet another beta-tubulin sequence designated TUBB4Q. This tubulin maps 80 kb proximal to the facioscapulohumeral muscular dystrophy (FSHD1) associated D4Z4 repeats on chromosome 4q35. The genomic structure contains four exons encoding a putative protein of 434 amino acids. The TUBB4Q nucleotide and protein sequence show 87% and 86% homology to beta2-tubulin, respectively. Although the genomic structure shows all functional aspects of a genuine gene, no transcript could be detected. TUBB4Q-related sequences were identified on multiple chromosomes. Since these sequences mutually exhibit a high nucleotide sequence homology, they presumably belong to a novel subfamily of beta-tubulin genes. Although the chromosome 4q35 tubulin-member probably represents a pseudogene, ectopic expression due to a postulated position effect variegation (PEV), makes TUBB4Q an ideal dominant-negative candidate gene for FSHD1. Copyright 2000 S. Karger AG, Basel

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Year:  2000        PMID: 10828619     DOI: 10.1159/000015518

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  10 in total

1.  A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes.

Authors:  Michel van Geel; Evan E Eichler; Amy F Beck; Zhihong Shan; Thomas Haaf; Silvère M van der Maarel; Rune R Frants; Pieter J de Jong
Journal:  Am J Hum Genet       Date:  2001-11-30       Impact factor: 11.025

2.  FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients.

Authors:  T Rijkers; G Deidda; S van Koningsbruggen; M van Geel; R J L F Lemmers; J C T van Deutekom; D Figlewicz; J E Hewitt; G W Padberg; R R Frants; S M van der Maarel
Journal:  J Med Genet       Date:  2004-11       Impact factor: 6.318

Review 3.  Emerging preclinical animal models for FSHD.

Authors:  Angela Lek; Fedik Rahimov; Peter L Jones; Louis M Kunkel
Journal:  Trends Mol Med       Date:  2015-03-20       Impact factor: 11.951

4.  Gene expression during normal and FSHD myogenesis.

Authors:  Koji Tsumagari; Shao-Chi Chang; Michelle Lacey; Carl Baribault; Sridar V Chittur; Janet Sowden; Rabi Tawil; Gregory E Crawford; Melanie Ehrlich
Journal:  BMC Med Genomics       Date:  2011-09-27       Impact factor: 3.063

Review 5.  DNA Methylation Profiling for Diagnosing Undifferentiated Sarcoma with Capicua Transcriptional Receptor (CIC) Alterations.

Authors:  Evelina Miele; Rita De Vito; Andrea Ciolfi; Lucia Pedace; Ida Russo; Maria Debora De Pasquale; Angela Di Giannatale; Alessandro Crocoli; Biagio De Angelis; Marco Tartaglia; Rita Alaggio; Giuseppe Maria Milano
Journal:  Int J Mol Sci       Date:  2020-03-06       Impact factor: 5.923

6.  Antagonism Between DUX4 and DUX4c Highlights a Pathomechanism Operating Through β-Catenin in Facioscapulohumeral Muscular Dystrophy.

Authors:  Massimo Ganassi; Nicolas Figeac; Magalie Reynaud; Huascar Pedro Ortuste Quiroga; Peter S Zammit
Journal:  Front Cell Dev Biol       Date:  2022-09-07

7.  DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation.

Authors:  Eugénie Ansseau; Dalila Laoudj-Chenivesse; Aline Marcowycz; Alexandra Tassin; Céline Vanderplanck; Sébastien Sauvage; Marietta Barro; Isabelle Mahieu; Axelle Leroy; India Leclercq; Véronique Mainfroid; Denise Figlewicz; Vincent Mouly; Gillian Butler-Browne; Alexandra Belayew; Frédérique Coppée
Journal:  PLoS One       Date:  2009-10-15       Impact factor: 3.240

8.  DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2.

Authors:  Xueqing Xu; Koji Tsumagari; Janet Sowden; Rabi Tawil; Alan P Boyle; Lingyun Song; Terrence S Furey; Gregory E Crawford; Melanie Ehrlich
Journal:  Nucleic Acids Res       Date:  2009-12       Impact factor: 16.971

9.  Recombinant chromosome 4 from a familial pericentric inversion: prenatal and adulthood wolf-hirschhorn phenotypes.

Authors:  Francesca Malvestiti; Francesco Benedicenti; Simona De Toffol; Sara Chinetti; Adelheid Höller; Beatrice Grimi; Gertrud Fichtel; Monica Braghetto; Cristina Agrati; Eleonora Bonaparte; Federico Maggi; Giuseppe Simoni; Francesca Romana Grati
Journal:  Case Rep Genet       Date:  2013-05-16

Review 10.  Facioscapulohumeral dystrophy: the path to consensus on pathophysiology.

Authors:  Rabi Tawil; Silvère M van der Maarel; Stephen J Tapscott
Journal:  Skelet Muscle       Date:  2014-06-10       Impact factor: 4.912

  10 in total

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