|
|
|
Licensing & Royalties >> Licensing Opportunities >> Abstract Details |
|
|
New Method for Quantification of Allele-Specific RNA Expression, that Can be Used for Detection of Various Genetic Disorders |
Description of Invention:
|
Available for licensing and commercial development is a new method for quantification of allele-specific RNA expression. This invention describes methods for simultaneously detecting the levels of expression of a plurality of different RNA transcripts expressed from a gene of interest in a subject or a cell. This is a simple assay to validate and quantify allele-specific silencing, by applying a combination of a fluorescent primer/probe set that specifically recognizes the targeted allele where the probe is labeled with one fluorophore, and a primer/probe set that specifically recognizes the normal allele, where the probe is labeled with another fluorophore in the same reaction tube. Furthermore, this method can be run on most real time PCR machines and requires very small amounts of RNA, less than 100 ng. This novel method, by comparing alleles within the same gene, expands on current real time PCR methods which compare one gene with another gene.
The invention also describes methods for validating the effectiveness and specificity of allele-specific siRNAs, kits for performing such assays, as well as methods for diagnosis of autosomal-dominant disorders, in which mutations in one allele result in a disease phenotype, such as Hutchinson-Gilford progeria, incontinentia pigmenti, neurofibromatosis, myotonic dystrophy, sialuria, Machado-Joseph disease, spinocerebellar ataxia, frontotemporal dementia, amyotrophic lateral sclerosis, slow channel congenital myasthenic syndrome, spinobulbar muscular dystrophy, as well as compound heterozygous autosomal recessive disorders. Other diseases that can be diagnosed include diabetes, cystic fibrosis, homocystenuria, Hermansky-Pudlak syndrome, cystinosis, Zellweger syndrome, beta-thalassemia, alkaptonuria, and cancer.
A variety of diseases appear to be mediated or accompanied by aberrant expression of one allele, often a mutant of a gene. Such differences in allelic expression can serve as the basis for diagnostic test for such conditions, and the ability to specifically silence the expression of detrimental alleles could be a therapeutic method for treating the disease, hence this novel method has very wide applications.
Marjan Huizing (NHGRI) Enriko Klootwijk (NHGRI) Paul Savelkoul (NHGRI) Carla Ciccone (NHGRI) William Gahl (NHGRI)
DHHS Reference No. E-146-2005/0 --
U.S. Provisional Application No. 60/718,321 filed 20 Sep 2005
Internal Medicine Gene Based Therapies Devices/Instrumentation Cancer
Cancer -Diagnostics-In Vitro-DNA Based Internal Medicine-Diagnostics-Cardiology-In Vitro Cancer -Diagnostics Devices/Instrumentation-Diagnostics Gene Based Therapies -Diagnostics Internal Medicine-Diagnostics
For Additional Information Please Contact:
| Cristina Thalhammer-Reyero PhD MBA
NIH Office of Technology Transfer
6011 Executive Blvd, Suite 325
Rockville, MD 20852-3804
Phone: (301) 435-4507
Email: thalhamc@mail.nih.gov
Fax: (301) 402-0220
Web Ref: 1336
Last Updated On: 5/06
|
|
|
|
|
|
|
|