Retinal dystrophy-associated protein and uses thereof
View Patent ↗Disclosed are methods and compositions for early diagnosis, monitoring and treatment of retinal dystrophy, age-related macular degeneration, Bardet-Biedel syndrome, Bassen-kornzweig syndrome, best disease, choroidema, gyrate atrophy, congenital amourosis, refsun syndrome, stargardt disease and Usher syndrome. In particular, the invention relates to a protein, termed “Rdcvf1,” that is differentially transcribed and expressed in subjects suffering from retinal dystrophies and the like, such as retinal dystrophy and age-related macular degeneration compared with non-sufferers, antibodies which recognize this protein, and methods for diagnosing such conditions.
1. A method of increasing the amount of Rod-Derived Cone Viability Factor (RDCVF) 1 polypeptide or RDCVF 2 polypeptide in the retinal cells of a subject suffering from retinitis pigmentosa characterized by the loss of the RDCVF 1 polypeptide or the RDCVF 2 polypeptide, the method comprising introducing a viral vector comprising a nucleic acid sequence encoding the RDCVF1 polypeptide or the RDCVF2 polypeptide into the retinal cells of the subject, wherein the nucleic acid is operably linked to a transcription control sequence, whereby expression of the nucleic acid in the retinal cells increases the amount of the RDCVF1 polypeptide or the RDCVF2 polypeptide.
2. The method of claim 1 further comprising the step of measuring the difference in the amount of the RDCVF1 polypeptide or the RDCVF2 polypeptide after introducing the viral vector compared to the amount of the RDCVF1 polypeptide or the RDCVF2 polypeptide prior to introducing the viral vector.
3. The method of claim 1 , wherein the vector is an adeno-associated virus.
4. The method of claim 1 , wherein the subject is a human.
5. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence set forth in SEQ ID NO:2, 4, 6, 8, 10, 12, or 14.
6. The method of claim 1 wherein the nucleic acid comprises the nucleic acid sequence set forth in SEQ ID NO:1, 3, 5, 7, 9, 11, or 13.