Claims
- 1. A method for identifying an RNA target for an allele specific RNA inhibitor, the method comprising:a) identifying in a population of subjects at least one sequence variance in an RNA encoded by a gene of interest; b) determining whether the secondary structure of the RNA comprising the at least one sequence variance differs from the secondary structure of an otherwise identical RNA not comprising the at least one sequence variance; and c) determining that the RNA comprising the at least one sequence variance is a target for an allele specific RNA inhibitor if the secondary structure of the RNA comprising the at least one sequence variance differs from the secondary structure of an otherwise identical RNA not comprising the at least one sequence variance.
- 2. The method of claim 1, wherein the sequence variance to be targeted occurs in a frequency range between 0.1:0.9 and 0.5:0.5 in a population of interest.
- 3. The method of claim 1, wherein the step of determining whether the secondary structure of the RNA comprising the at least one sequence variance differs from the secondary structure of an otherwise identical RNA not comprising the at least one sequence variance comprises using a nuclease selected from the group consisting of T1, T2, S1, U2, CL3, V1, A, PhyM, N.c. nuclease and Rnase.
- 4. The method of claim 1, wherein the RNA target comprises an undesirable allele.
- 5. The method of claim 1, wherein the RNA target comprises an allele associated with an autosomal dominant disease.
- 6. The method of claim 1, wherein the autosomal dominant disease is selected from the group consisting of Huntington's disease, cervical vertebrate fusion, keratitis-ichthyosis-deafness syndrome, progressive external ophthalmoplegia, type 3, progressive external ophthalmoplegia, type 2, spastic paraplegia 6, progressive external ophthalmoplegia, pituitary dwarfism due to isolated growth hormone deficiency, distal renal tubular acidosis, vitamin D-resistant rickets, scapuloilioperoneal atrophy with cardiopathy, spastic paraplegia 4, spastic paraplegia 3, type II osteopetrosis, lamellar ichthyosis, nonsyndromic sensorineural 3 deafness, iridogoniodysgenesis, type 2, spinocerebellar ataxia 7, microcephaly, torsion dystonia 1, hereditary multi-infarct type dementia, pseudoxanthoma elasticum, autosomal dominant Lewy body in Parkinson disease, autosomal dominant nonsyndromic sensorineural 2 deafness, hypertelorism with esophageal abnormality and hypospadias, microcephaly with chorioretinopathy, diamond-blackfan anemia, hyperinsulinism, ectodermal dysplasia 3, nonsyndromic snsorineural 8 deafness, Larsen syndrome, hypoplastic local amelogenesis imperfecta 2, polycystic kidney disease 3, congenital nystagmus 2, Ehlers-Danlos syndrome, type IV, mitochondrial DNA breakage syndrome secondary to nuclear mutation, and retinal cone dystrophy 2.
- 7. The method of claim 1, wherein the RNA target comprises an allele of an essential gene which is deleted in a proliferative disorder.
- 8. The method of claim 1, wherein the step of determining whether the secondary structure of the RNA comprising the at least one sequence variance differs from the secondary structure of an otherwise identical RNA not comprising the at least one sequence variance comprises by chemical probing with a chemical selected from the group consisting of dimethylsulfate, diethylpryocarbonate, CMCT, kethoxal, bisulfite, ethylnitrosourea, MPE-Fe(II), and Fe(II)-EDTA.
- 9. A method for identifying an RNA target for an allele specific agent, the method comprising:a) identifying in a population of subjects at least one sequence variance in an RNA encoded by a gene of interest; b) determining whether the secondary structure of the RNA comprising the at least one sequence variance differs from the secondary structure of an otherwise identical RNA not comprising the at least one sequence variance; c) determining that the RNA comprising the at least one sequence variance is a candidate target for an allele specific agent if the secondary structure of the RNA comprising the at least one sequence variance differs from the secondary structure of an otherwise identical RNA not comprising the at least one sequence variance; d) contacting RNA comprising the at least one sequence variance and an otherwise identical RNA not comprising the at least one sequence variance with an allele specific agent; e) determining that the RNA comprising the at least one sequence variance is a target for an allele specific agent if the candidate allele specific agent selectively binds to the RNA comprising the at least one sequence variance differs relative to the otherwise identical RNA not comprising the at least one sequence variance.
RELATED APPLICATION
This application claims the benefit of Shen et al., U.S. Provisional Application No. 60/122,199, filed Mar. 1, 1999, entitled METHODS FOR TARGETING RNA MOLECULES, which is hereby incorporated by reference in its entirety, including drawings.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
6214545 |
Dong et al. |
Apr 2001 |
B1 |
Non-Patent Literature Citations (3)
Entry |
Millington-Ward et al. Strategems in vitro for gene therapies directed to dominant mutations Human Molecular Genetics, 1997 vol. 6 No. 9 1415-1426.* |
Millington-Ward, Sophia, et al. “Strategems in vitro for gene therapies directed to dominant mutations” Human Molecular Genetics, 1997, vol. 6, No. 9, 1415-1426. |
Shen, Ling X. et al. “Single-nucleotide polymorphisms can cause different structural folds in mRNA” Proc. Natl. Acad. Sci. USA, vol. 96, 7871-7876, Jul. 1999. |
Provisional Applications (1)
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Number |
Date |
Country |
|
60/122199 |
Mar 1999 |
US |