A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa

S. Amer Riazuddin, Muhammad Iqbal, Yue Wang, Tomohiro Masuda, Yuhng Chen, Sara Bowne, Lori S. Sullivan, Naushin H. Waseem, Shomi Bhattacharya, Stephen P. Daiger, Kang Zhang, Shaheen N. Khan, Sheikh Riazuddin, J. Fielding Hejtmancik, Paul A. Sieving, Donald J. Zack, Nicholas Katsanis

Research output: Contribution to journalArticlepeer-review

77 Scopus citations


Tissue-specific alternative splicing is an important mechanism for providing spatiotemporal protein diversity. Here we show that an in-frame splice mutation in BBS8, one of the genes involved in pleiotropic Bardet-Biedl syndrome (BBS), is sufficient to cause nonsyndromic retinitis pigmentosa (RP). A genome-wide scan of a consanguineous RP pedigree mapped the trait to a 5.6 Mb region; subsequent systematic sequencing of candidate transcripts identified a homozygous splice-site mutation in a previously unknown BBS8 exon. The allele segregated with the disorder, was absent from controls, was completely invariant across evolution, and was predicted to lead to the elimination of a 10 amino acid sequence from the protein. Subsequent studies showed the exon to be expressed exclusively in the retina and enriched significantly in the photoreceptor layer. Importantly, we found this exon to represent the major BBS8 mRNA species in the mammalian photoreceptor, suggesting that the encoded 10 amino acids play a pivotal role in the function of BBS8 in this organ. Understanding the role of this additional sequence might therefore inform the mechanism of retinal degeneration in patients with syndromic BBS or other related ciliopathies.

Original languageEnglish (US)
Pages (from-to)805-812
Number of pages8
JournalAmerican journal of human genetics
Issue number5
StatePublished - May 14 2010

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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