| Literature DB >> 10828619 |
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, BaselEntities:
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Year: 2000 PMID: 10828619 DOI: 10.1159/000015518
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171