KNAW Repository

A mutation in Myo15 leads to Usher-like symptoms in LEW/Ztm-ci2 rats

Held, N. and Smits, B.M. and Gockeln, R. and Schubert, S. and Nave, H. and Northrup, E. and Cuppen, E. and Hedrich, H.J. and Wedekind, D. (2011) A mutation in Myo15 leads to Usher-like symptoms in LEW/Ztm-ci2 rats. PLoS One, 6, e15669-. ISSN 1932-6203.

PDF - Published Version
Available under License Creative Commons Attribution Non-commercial Share Alike.


Official URL:


The LEW/Ztm-ci2 rat is an animal model for syndromal deafness that arose from a spontaneous mutation. Homozygous animals show locomotor abnormalities like lateralized circling behavior. Additionally, an impaired vision can be observed in some animals through behavioral studies. Syndromal deafness as well as retinal degeneration are features of the Usher syndrome in humans. In the present study, the mutation was identified as a base substitution (T->C) in exon 56 of Myo15, leading to an amino acid exchange from leucine (Leu) to proline (Pro) within the carboxy-terminal MyTH4 domain in the proteins' tail region. Myo15 mRNA was expressed in the retina as demonstrated for the first time with the help of in-situ hybridization and PCR. To characterize the visual phenotype, rats were examined by scotopic and photopic electroretinography and, additionally, histological analyses of the retinas were conducted. The complete loss of sight was detected along with a severe degeneration of photoreceptor cells. Interestingly, the manifestation of the disease does not solely depend on the mutation, but also on environmental factors. Since the LEW/Ztm-ci2 rat features the entire range of symptoms of the human Usher syndrome we think that this strain is an appropriate model for this disease. Our findings display that mutations in binding domains of myosin XV do not only cause non-syndromic hearing loss but can also lead to syndromic disorders including retinal dysfunction. [KEYWORDS: Amino Acid Sequence, Animals, Base Sequence, Electroretinography, Environment, Exons/genetics, Female, Gene Expression Regulation/radiation effects, Humans, In Situ Hybridization, Light, Male, Molecular Sequence Data, Mutation/ genetics, Myosins/chemistry/ genetics, Phenotype, RNA, Messenger/genetics/metabolism, Rats, Rats, Mutant Strains, Retinal Degeneration/complications/pathology/physiopathology, Retinal Rod Photoreceptor Cells/physiology/radiation effects, Reverse Transcriptase P

Item Type:Article
Institutes:Hubrecht Instituut
ID Code:12662
Deposited On:19 Sep 2012 15:34
Last Modified:14 Oct 2012 19:03

Repository Staff Only: item control page