Looking into Eyes: Rhodopsin Pathologies in Drosophila

  • Ana Griciuc
  • Liviu AronEmail author
  • Marius UeffingEmail author
Conference paper
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 723)


The detailed examination of eye structure and function in numerous Drosophila mutants has provided unprecedented insights into retinal physiology and pathology. Many Drosophila mutants that undergo retinal degeneration (RD) exhibit structural and/or dynamic alterations of the photon receptor rhodopsin, and similar defects cause retinitis pigmentosa (RP) in humans. Here, we consider how the use of Drosophila has advanced our understanding of RP and highlight new mechanisms underlying rhodopsin-mediated pathologies in the retina.


Retinitis pigmentosa Retinal degeneration Rhodopsin Drosophila Photoreceptor Retina Phototransduction Autophagy ER stress 



Work in the Ueffing laboratory is supported by the EU Grant NEUROTRAIN (MEST-CT-2005-020235), RETNET (MRTN-CT-2003-504003) and EVI-GENORET (LSHG-CT-2005-512036 to MU).


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Copyright information

© Springer Science+Business Media, LLC 2012

Authors and Affiliations

  1. 1.Department of Protein ScienceHelmholtz Zentrum Muenchen-German Research Center for Environmental HealthNeuherbergGermany
  2. 2.Institute for Ophthalmic Research, Center for OphtalmologyUniversity of TuebingenTuebingenGermany
  3. 3.Department of PathologyHarvard Medical SchoolBostonUSA

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