Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis.

Abstract

Leber congenital amaurosis (LCA) is the most severe form of retinal dystrophy with an onset in the first year of life. The most frequent genetic cause of LCA, accounting for up to 15% of all LCA cases in Europe and North-America, is a mutation (c.2991+1655AG) in intron 26 of CEP290. This mutation generates a cryptic splice donor site resulting in the insertion of an aberrant exon (exon X) containing a premature stop codon to CEP290 mRNA. In order to study the pathophysiology of the intronic CEP290 mutation, we generated two humanized knock-in mouse models each carrying ~6.3 kb of the human CEP290 gene, either with or without the intronic mutation. Transcriptional characterization of these mouse models revealed an unexpected splice pattern of CEP290 mRNA, especially in the retina. In both models, a new cryptic exon (coined exon Y) was identified in ~5 to 12% of all Cep290 transcripts. This exon Y was expressed in all murine tissues analyzed but not detected in human retina or fibroblasts of LCA patients. In addition, exon x that is characteristic of LCA in humans, was expressed at only very low levels in the retina of the LCA mouse model. Western blot and immunohistochemical analyses did not reveal any differences between the two transgenic models and wild-type mice. Together, our results show clear differences in the recognition of splice sites between mice and humans, and emphasize that care is warranted when generating animal models for human genetic diseases caused by splice mutations.

• Authors: Alejandro Garanto, Sylvia E C van Beersum, Theo A Peters, Ronald Roepman, Frans P M Cremers, Rob W J Collin
• Journal: PloS one (PLoS One) Vol. 8 Issue 11 Pg. e79369 ( 2013) ISSN: 1932-6203 [Electronic] United States
• PMID: 24223178 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antigens, Neoplasm
• Cell Cycle Proteins
• Cep290 protein, human
• Cytoskeletal Proteins
• Neoplasm Proteins

Topics

• Animals
• Antigens, Neoplasm (genetics)
• Cell Cycle Proteins
• Cell Line
• Cytoskeletal Proteins
• Disease Models, Animal
• Exons (genetics)
• Female
• Gene Knock-In Techniques
• Humans
• Leber Congenital Amaurosis (genetics)
• Mice
• Neoplasm Proteins (genetics)
• Pregnancy
• RNA Splicing
• Retina (metabolism)
• Species Specificity
• Transcription, Genetic (genetics)