Mutation of the receptor tyrosine kinase gene Mertkin the retinal dystrophic RCS rat

Authors: D’Cruz, Patricia M.; Yasumura, Douglas1; Weir, Jessica; Matthes, Michael T.1; Abderrahim, Hadi; LaVail, Matthew M.1; Vollrath, Douglas

Source: Human Molecular Genetics, Volume 9, Number 4, 1 March 2000 , pp. 645-651(7)

Publisher: Oxford University Press

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Abstract:

Vertebrate photoreceptor cells are the basic sensory apparatus of the retina, capable of converting the energy of absorbed photons into neuronal signals. The proximal portions of mammalian photoreceptor outer segments are synthesized daily by cell bodies, and outer segment tips are shed with a circadian rhythm, resulting in a complete turnover of outer segments about every 9 days. The shed outer segments are phagocytosed by adjacent retinal pigment epithelial (RPE) cells, and metabolites are recycled to photoreceptors. The Royal College of Surgeons (RCS) rat is a widely studied, classic model of recessively inherited retinal degeneration in which the RPE fails to phagocytose shed outer segments, and photoreceptor cells subsequently die. We have used a positional cloning approach to study the rdy (retinal dystrophy) locus of the RCS rat. Within a 0.3 cM genetic inclusion interval, we have discovered a small deletion of RCS DNA that disrupts the gene encoding the receptor tyrosine kinase Mertk. The deletion includes the splice acceptor site upstream of the second coding exon of Mertk and results in a shortened transcript that lacks this exon. The aberrant transcript joins the first and third coding exons, leading to a frameshift and a translation termination signal 20 codons after the AUG. The concordance of these and other data indicate that Mertk is probably the gene for rdy. Our results provide genetic evidence for an essential role of a receptor tyrosine kinase in a specialized form of phagocytosis and suggest a molecular model for ingestion of outer segments by RPE cells.

Document Type: Research article

Affiliations: 1: Departments of Anatomy and Ophthalmology, University of California, San Francisco School of Medicine, San Francisco, CA 94143-0730, USA

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