RGD Reference Report - Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. - Rat Genome Database

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Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia.

Authors: Slaugenhaupt, SA  Blumenfeld, A  Gill, SP  Leyne, M  Mull, J  Cuajungco, MP  Liebert, CB  Chadwick, B  Idelson, M  Reznik, L  Robbins, C  Makalowska, I  Brownstein, M  Krappmann, D  Scheidereit, C  Maayan, C  Axelrod, FB  Gusella, JF 
Citation: Slaugenhaupt SA, etal., Am J Hum Genet. 2001 Mar;68(3):598-605. Epub 2001 Jan 22.
RGD ID: 5129156
Pubmed: (View Article at PubMed) PMID:11179008

Familial dysautonomia (FD; also known as "Riley-Day syndrome"), an Ashkenazi Jewish disorder, is the best known and most frequent of a group of congenital sensory neuropathies and is characterized by widespread sensory and variable autonomic dysfunction. Previously, we had mapped the FD gene, DYS, to a 0.5-cM region on chromosome 9q31 and had shown that the ethnic bias is due to a founder effect, with >99.5% of disease alleles sharing a common ancestral haplotype. To investigate the molecular basis of FD, we sequenced the minimal candidate region and cloned and characterized its five genes. One of these, IKBKAP, harbors two mutations that can cause FD. The major haplotype mutation is located in the donor splice site of intron 20. This mutation can result in skipping of exon 20 in the mRNA of patients with FD, although they continue to express varying levels of wild-type message in a tissue-specific manner. RNA isolated from lymphoblasts of patients is primarily wild-type, whereas only the deleted message is seen in RNA isolated from brain. The mutation associated with the minor haplotype in four patients is a missense (R696P) mutation in exon 19, which is predicted to disrupt a potential phosphorylation site. Our findings indicate that almost all cases of FD are caused by an unusual splice defect that displays tissue-specific expression; and they also provide the basis for rapid carrier screening in the Ashkenazi Jewish population.


Disease Annotations    
Riley-Day syndrome  (IAGP,ISO)

Objects Annotated

Genes (Rattus norvegicus)
Elp1  (elongator acetyltransferase complex subunit 1)

Genes (Mus musculus)
Elp1  (elongator complex protein 1)

Genes (Homo sapiens)
ELP1  (elongator acetyltransferase complex subunit 1)

Additional Information