X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and novel gene containing WD-40 repeats

Maria T. Bassi, Rajkumar S. Ramesar, Barbara Caciotti, Ingrid M. Winship, Alessandro De Grandi, Mirko Riboni, Philip L. Townes, Peter Beighton, Andrea Ballabio, Giuseppe Borsani

Research output: Contribution to journalArticlepeer-review


We have identified a novel gene, transducin (β)-like 1 (TBL1), in the Xp22.3 genomic region, that shows high homology with members of the WD-40- repeat protein family. The gene contains 18 exons spanning ~150 kb of the genomic region adjacent to the ocular albinism gene (OA1) on the telomeric side. However, unlike OA1, TBL1 is transcribed from telomere to centromere. Northern analysis indicates that TBL1 is ubiquitously expressed, with two transcripts of ~2.1 kb and 6.0 kb. The open reading frame encodes a 526- amino acid protein, which shows the presence of six β-transducin repeats (WD-40 motif) in the C-terminal domain. The homology with known β-subunits of G proteins and other WD-40-repeat containing proteins is restricted to the WD-40 motif. Genomic analysis revealed that the gene is either partly or entirely deleted in patients carrying Xp22.3 terminal deletions. The complexity of the contiguous gene-syndrome phenotype shared by these patients depends on the number of known disease genes involved in the deletions. Interestingly, one patient carrying a microinterstitial deletion involving the 3' portion of both TBL1 and OA1 shows the OA1 phenotype associated with X-linked late-onset sensorineural deafness. We postulate an involvement of TBL1 in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype.

Original languageEnglish
Pages (from-to)1604-1616
Number of pages13
JournalAmerican Journal of Human Genetics
Issue number6
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Genetics


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