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

被引:24
作者
van Geel, M
van Deutekom, JCT
van Staalduinen, A
Lemmers, RJLF
Dickson, MC
Hofker, MH
Padberg, GW
Hewitt, JE
de Jong, PJ
Frants, RR
机构
[1] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
[2] Leiden Univ, Med Ctr, MGC, Dept Human & Clin Genet, Leiden, Netherlands
[3] Univ Manchester, Sch Biol Sci, Manchester, Lancs, England
[4] Univ Nijmegen Hosp, Dept Neurol, NL-6500 HB Nijmegen, Netherlands
来源
CYTOGENETICS AND CELL GENETICS | 2000年 / 88卷 / 3-4期
关键词
D O I
10.1159/000015518
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 beta 2-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 (C) 2000 S. Karger AG, Basel.
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页码:316 / 321
页数:6
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