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

      Cytogenetics and cell genetics
      Alleles, Amino Acid Sequence, Amino Acid Substitution, Base Sequence, Chromosomes, Human, Pair 4, genetics, Cloning, Molecular, Exons, Genetic Linkage, Humans, Introns, Molecular Sequence Data, Multigene Family, Muscular Dystrophy, Facioscapulohumeral, Physical Chromosome Mapping, Polymerase Chain Reaction, Promoter Regions, Genetic, Protein Structure, Tertiary, Pseudogenes, RNA, Messenger, analysis, Telomere, Tubulin, chemistry

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          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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