In vitro Analysis of Ribozyme-mediated Knockdown of an ADRP Associated Rhodopsin Mutation

  • Dibyendu Chakraborty
  • Patrick Whalen
  • Alfred S. Lewin
  • Muna I. Naash
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 613)

Retinitis Pigmentosa (RP) is a group of retinal degenerative diseases that are characterized mainly by the loss of rod photoreceptor cells. RP can be sub divided into 3 classes, autosomal dominant, autosomal recessive, and X- linked RP, where the mutant gene exists on the sex chromosome (X) (Hartong et al., 2006; Wang et al., 2005). Mutations in rhodopsin are the most common cause of the autosomaldominant form of RP (ADRP). More than 100 mutations in rhodopsin account for approximately 30 of ADRP cases with varying severity of visual impairment (Dryja et al., 1991). Based on in vitro studies (Sung et al., 1993; Sung et al., 1991), rhodopsin mutations that are similar to wild-type in terms of expression levels, folding and formation of functional photopigment are considered Class 1 mutations.


Retinitis Pigmentosa Retinal Degeneration Opsin Gene Hammerhead Ribozyme Photoreceptor Degeneration 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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Copyright information

© Springer Science+Business Media, LLC 2008

Authors and Affiliations

  • Dibyendu Chakraborty
    • Patrick Whalen
      • 2
    • Alfred S. Lewin
      • 3
    • Muna I. Naash
      • 1
    1. 1.Department of Cell BiologyUniversity of Oklahoma Health Sciences CenterOklahoma City
    2. 2.Departments of Molecular Genetics and the Center for Vision ScienceUniversity of FloridaGainesvilleUSA
    3. 3.Departments of Molecular Genetics and the Center for Vision Science, Department of Molecular Genetics and MicrobiologyUniversity of Florida, University of Florida College of MedicineGainesvilleUSA

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