RNAi-based suppression and replacement of rds-peripherin in retinal organotypic culture
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
Abstract
Extensive mutational heterogeneity presents a significant barrier to the development of therapeutics for RDS-peripherin-linked autosomal-dominant retinitis pigmentosa (RP), for which more than 50 disease-related mutations have been identified to date. Mutation-independent suppression, using RNA interference (RNAi), together with simultaneous expression of a replacement rds gene (r-rds, which has been altered to escape suppression but nevertheless encodes wild-type protein) has been explored in COS-7 cells and mouse retinal explants. The efficacy of small interfering and short hairpin RNAs (si/shRNAs) silencing mouse rds, and the function of r-rds (containing degenerate substitutions in the RNAi target sequence) were analyzed at transcript (RT-PCR) and protein (ELISA) levels in COS-7 cells. "Dual-" and "triple-expression" constructs carrying the shRNA suppressor and the marker EGFP with or without the r-rds cassette were electroporated in vitro into retinal explants from 1-day-old pups. The retinae were dissociated at day 14, and transduced cells were FACS-sorted using the coexpressed EGFP marker and analyzed by RT-PCR. si/shRNAs decreased rds mRNA and protein expression by up to 82%, while r-rds was protected from suppression in COS-7 cells. Similarly, efficient RNAi-mediated suppression of endogenous rds was detected in retinal explants, while concomitant rescue of r-rds was also achieved. These data validate the concept of RNAi-based suppression coupled with replacement technology for the development of therapies targeting RDS-linked autosomal-dominant RP, and suggest that such approaches could potentially be used for other autosomal-dominant diseases with similarly extensive intragenic heterogeneity.
Details
Originalsprache | Englisch |
---|---|
Seiten (von - bis) | 260-8 |
Seitenumfang | 9 |
Fachzeitschrift | Human mutation |
Jahrgang | 27 |
Ausgabenummer | 3 |
Publikationsstatus | Veröffentlicht - März 2006 |
Peer-Review-Status | Ja |
Extern publiziert | Ja |
Externe IDs
Scopus | 33645224383 |
---|---|
ORCID | /0000-0001-9467-7677/work/161888214 |
Schlagworte
Schlagwörter
- Animals, COS Cells, Cell Separation, Chlorocebus aethiops, DNA Mutational Analysis/methods, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, Gene Silencing, Intermediate Filament Proteins/genetics, Membrane Glycoproteins/genetics, Mice, Mutation, Nerve Tissue Proteins/genetics, Peripherins, RNA Interference, RNA, Small Interfering/metabolism, Retina/metabolism, Retinitis Pigmentosa/genetics, Reverse Transcriptase Polymerase Chain Reaction