Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion

• Published in: Pediatric nephrology (Berlin, West) West), 2010-07, Vol.25 (7), p.1343-1348
• Main Authors: Morisada, Naoya, Rendtorff, Nanna Dahl, Nozu, Kandai, Morishita, Takahiro, Miyakawa, Takayuki, Matsumoto, Tohru, Hisano, Satoshi, Iijima, Kazumoto, Tranebjærg, Lisbeth, Shirahata, Akira, Matsuo, Masafumi, Kusuhara, Koichi
• Format: Article
• Language: English
• Subjects: Abnormalities, Multiple - genetics; Abnormalities, Multiple - pathology; Analysis; Branchial Region - abnormalities; Brief Report; Child; Deafness; DNA; Ear - abnormalities; Female; Gene Deletion; Gene Expression Regulation, Developmental; Gene mutations; Genes; Humans; Intracellular Signaling Peptides and Proteins - genetics; Kidney - abnormalities; Long Interspersed Nucleotide Elements - genetics; Medicine; Medicine & Public Health; Mutagenesis, Insertional - genetics; Nephrology; Nuclear Proteins - genetics; Nucleic Acid Amplification Techniques; Pediatrics; Protein Tyrosine Phosphatases - genetics; Renal Insufficiency - genetics; RNA; RNA, Messenger - metabolism; Syndrome; Urology
• ISSN: 0931-041X; 1432-198X
• DOI: 10.1007/s00467-010-1445-x

A 7-year-old Japanese girl with conductive deafness and preauricular fistulae developed proteinuria. She had renal insufficiency, and ultrasound revealed bilateral small kidneys. These findings indicated that she had branchio-oto-renal (BOR) syndrome. In the present patient, we identified, by using multiplex ligation-dependent probe amplification (MLPA) analysis, a heterozygous EYA1 gene deletion comprising at least exons 5 to 7. In her parents, we did not detect any deletion in EYA1 by MLPA, so the deletion was a de novo mutation. PCR analysis and sequencing of patient DNA revealed a heterozygous ∼17 kb EYA1 deletion starting from the eight last bases of exon 4 and proceeding to base 1,217 of intron 7. Furthermore, in place of this deleted region was inserted a 3756-bp-long interspersed nuclear elements-1 (LINE-1, L1). Accordingly, RT-PCR showed that exons 4–7 were not present in EYA1 mRNA expressed from the mutated allele. Although there are reports of L1 element insertion occurring in various human diseases, this is the first report of a large EYA1 deletion in combination with L1 element insertion.