GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.

Have any questions? Please email us at ecoliwiki@gmail.com

TableEdit

Jump to: navigation, search

PMID:19657028

You don't have sufficient rights on this wiki to edit tables. Perhaps you need to log in. Changes you make in the Table editor will not be saved back to the wiki

See Help for Help on this wiki. See the documentation for how to use the table editor

Citation

Yamashita, T, Liu, J, Gao, J, LeNoue, S, Wang, C, Kaminoh, J, Bowne, SJ, Sullivan, LS, Daiger, SP, Zhang, K, Fitzgerald, ME, Kefalov, VJ and Zuo, J (2009) Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa. J. Neurosci. 29:9748-60

Abstract

Retinitis pigmentosa 1 (RP1) is a common inherited retinopathy with variable onset and severity. The RP1 gene encodes a photoreceptor-specific, microtubule-associated ciliary protein containing the doublecortin (DCX) domain. Here we show that another photoreceptor-specific Rp1-like protein (Rp1L1) in mice is also localized to the axoneme of outer segments (OSs) and connecting cilia in rod photoreceptors, overlapping with Rp1. Rp1L1-/- mice display scattered OS disorganization, reduced electroretinogram amplitudes, and progressive photoreceptor degeneration, less severe and slower than in Rp1-/- mice. In single rods of Rp1L1-/-, photosensitivity is reduced, similar to that of Rp1-/-. While individual heterozygotes are normal, double heterozygotes of Rp1 and Rp1L1 exhibit abnormal OS morphology and reduced single rod photosensitivity and dark currents. The electroretinogram amplitudes of double heterozygotes are more reduced than those of individual heterozygotes combined. In support, Rp1L1 interacts with Rp1 in transfected cells and in retina pull-down experiments. Interestingly, phototransduction kinetics are normal in single rods and whole retinas of individual or double Rp1 and Rp1L1 mutant mice. Together, Rp1 and Rp1L1 play essential and synergistic roles in affecting photosensitivity and OS morphogenesis of rod photoreceptors. Our findings suggest that mutations in RP1L1 could underlie retinopathy or modify RP1 disease expression in humans.

Links

PubMed PMC2748320 Online version:10.1523/JNEUROSCI.5854-08.2009

Keywords

Animals; Axoneme/metabolism; Electroretinography; Eye Proteins/genetics; Eye Proteins/metabolism; Genotype; Kinetics; Mice; Mice, Knockout; Microtubule-Associated Proteins/genetics; Microtubule-Associated Proteins/metabolism; Photic Stimulation; RNA, Messenger/genetics; RNA, Messenger/metabolism; Retina/metabolism; Retina/physiology; Retina/ultrastructure; Retinal Rod Photoreceptor Cells/metabolism; Retinal Rod Photoreceptor Cells/physiology; Retinal Rod Photoreceptor Cells/ultrastructure; Retinitis Pigmentosa/complications; Retinitis Pigmentosa/metabolism; Rhodopsin/metabolism; Signal Transduction; Vision, Ocular/physiology

public



Cancel