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Trends Mol Med. 2001 Sep;7(9):414-21.

Unfolding retinal dystrophies: a role for molecular chaperones?

Author information

1
Dept of Pathology, Institute of Ophthalmology, University College London, 11-43 Bath Street, London, UK EC1V 9EL.

Abstract

Inherited retinal dystrophy is a major cause of blindness worldwide. Recent molecular studies have suggested that protein folding and molecular chaperones might play a major role in the pathogenesis of these degenerations. Incorrect protein folding could be a common consequence of causative mutations in retinal degeneration disease genes, particularly mutations in the visual pigment rhodopsin. Furthermore, several retinal degeneration disease genes have recently been identified as putative facilitators of correct protein folding, molecular chaperones, on the basis of sequence homology. We also consider whether manipulation of chaperone levels or chaperone function might offer potential novel therapies for retinal degeneration.

PMID:
11530337
[Indexed for MEDLINE]

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