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Uncoupling of photoreceptor peripherin/rds fusogenic activity from biosynthesis, subunit assembly, and targeting: a potential mechanism for pathogenic effects.
Ritter LM, Boesze-Battaglia K, Tam BM, Moritz OL, Khattree N, Chen SC, Goldberg AF.
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Inherited defects in the RDS gene cause a multiplicity of progressive retinal diseases in humans. The gene product, peripherin/rds (P/rds), is a member of the tetraspanin protein family required for normal vertebrate photoreceptor outer segment (OS) architecture. Although its molecular function remains uncertain, P/rds has been suggested to catalyze membrane fusion events required for the OS renewal process. This study investigates the importance of two charged residues within a predicted C-terminal helical region for protein biosynthesis, localization, and interaction with model membranes. Targeted mutagenesis was utilized to neutralize charges at Glu(321) and Lys(324) individually and in combination to generate three mutant variants. Studies were conducted on variants expressed as 1) full-length P/rds in COS-1 cells, 2) glutathione S-transferase fusion proteins in Escherichia coli, and 3) membrane-associated green fluorescent protein fusion proteins in transgenic Xenopus laevis. None of the mutations affected biosynthesis of full-length P/rds in COS-1 cells as assessed by Western blotting, sedimentation velocity, and immunofluorescence microscopy. Although all mutations reside within a recently identified localization signal, none altered the ability of this region to direct OS targeting in transgenic X. laevis retinas. In contrast, individual or simultaneous neutralization of the charged amino acids Glu(321) and Lys(324) abolished the ability of the C-terminal domain to promote model membrane fusion as assayed by lipid mixing. These results demonstrate that, although overlapping, C-terminal determinants responsible for OS targeting and fusogenicity are separable and that fusogenic activity has been uncoupled from other protein properties. The observation that subunit assembly and OS targeting can both proceed normally in the absence of fusogenic activity suggests that properly assembled and targeted yet functionally altered proteins could potentially generate pathogenic effects within the vertebrate photoreceptor.
Arikawa,
Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration.
1992, Pubmed
Arikawa,
Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration.
1992,
Pubmed Boesze-Battaglia,
A soluble peripherin/Rds C-terminal polypeptide promotes membrane fusion and changes conformation upon membrane association.
2003,
Pubmed Boesze-Battaglia,
A peptide analogue to a fusion domain within photoreceptor peripherin/rds promotes membrane adhesion and depolarization.
2000,
Pubmed Boesze-Battaglia,
Photoreceptor renewal: a role for peripherin/rds.
2002,
Pubmed Boesze-Battaglia,
Fusion between retinal rod outer segment membranes and model membranes: a role for photoreceptor peripherin/rds.
1998,
Pubmed Boesze-Battaglia,
Fusion between retinal rod outer segment membranes and model membranes: functional assays and role for peripherin/rds.
2000,
Pubmed Boesze-Battaglia,
Purification and light-dependent phosphorylation of a candidate fusion protein, the photoreceptor cell peripherin/rds.
1997,
Pubmed Boesze-Battagliaa,
Peripherin/rds fusogenic function correlates with subunit assembly.
2002,
Pubmed Chang,
Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice.
1993,
Pubmed Clarke,
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.
2000,
Pubmed Connell,
Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane.
1990,
Pubmed Démant,
The map position of the rds gene on the 17th chromosome of the mouse.
1979,
Pubmed Dryja,
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa.
1997,
Pubmed Epand,
Fusion peptides and the mechanism of viral fusion.
2003,
Pubmed Farrar,
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa.
1991,
Pubmed Felbor,
Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS gene.
1997,
Pubmed Gething,
Studies on the mechanism of membrane fusion: site-specific mutagenesis of the hemagglutinin of influenza virus.
1986,
Pubmed Goldberg,
Cysteine residues of photoreceptor peripherin/rds: role in subunit assembly and autosomal dominant retinitis pigmentosa.
1998,
Pubmed Goldberg,
Folding and subunit assembly of photoreceptor peripherin/rds is mediated by determinants within the extracellular/intradiskal EC2 domain: implications for heterogeneous molecular pathologies.
2001,
Pubmed Goldberg,
Heterologous expression of photoreceptor peripherin/rds and Rom-1 in COS-1 cells: assembly, interactions, and localization of multisubunit complexes.
1995,
Pubmed Goldberg,
Subunit composition of the peripherin/rds-rom-1 disk rim complex from rod photoreceptors: hydrodynamic evidence for a tetrameric quaternary structure.
1996,
Pubmed Goldberg,
Expression and characterization of peripherin/rds-rom-1 complexes and mutants implicated in retinal degenerative diseases.
2000,
Pubmed Goldberg,
Defective subunit assembly underlies a digenic form of retinitis pigmentosa linked to mutations in peripherin/rds and rom-1.
1996,
Pubmed Grover,
Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations.
2002,
Pubmed Grüning,
Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa.
1994,
Pubmed Han,
Membrane structure and fusion-triggering conformational change of the fusion domain from influenza hemagglutinin.
2001,
Pubmed Hawkins,
Development and degeneration of retina in rds mutant mice: photoreceptor abnormalities in the heterozygotes.
1985,
Pubmed Kajiwara,
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.
1991,
Pubmed Kedzierski,
Analysis of the rds/peripherin.rom1 complex in transgenic photoreceptors that express a chimeric protein.
1999,
Pubmed Kedzierski,
Three homologs of rds/peripherin in Xenopus laevis photoreceptors that exhibit covalent and non-covalent interactions.
1996,
Pubmed
,
Xenbase Kedzierski,
Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors.
1997,
Pubmed Kedzierski,
Transgenic analysis of rds/peripherin N-glycosylation: effect on dimerization, interaction with rom1, and rescue of the rds null phenotype.
1999,
Pubmed Kedzierski,
Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa.
2001,
Pubmed Kneller,
Improvements in protein secondary structure prediction by an enhanced neural network.
1990,
Pubmed Kohl,
RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.
1997,
Pubmed Kohl,
The role of the peripherin/RDS gene in retinal dystrophies.
1998,
Pubmed Korte,
Role of the Glu residues of the influenza hemagglutinin fusion peptide in the pH dependence of fusion activity.
2001,
Pubmed Kroll,
Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation.
1996,
Pubmed
,
Xenbase Lau,
Oligomerization of fusogenic peptides promotes membrane fusion by enhancing membrane destabilization.
2004,
Pubmed Loewen,
Molecular characterization of peripherin-2 and rom-1 mutants responsible for digenic retinitis pigmentosa.
2001,
Pubmed Loewen,
The role of subunit assembly in peripherin-2 targeting to rod photoreceptor disk membranes and retinitis pigmentosa.
2003,
Pubmed
,
Xenbase Loewen,
Disulfide-mediated oligomerization of Peripherin/Rds and Rom-1 in photoreceptor disk membranes. Implications for photoreceptor outer segment morphogenesis and degeneration.
2000,
Pubmed Mayer,
Vesicles of variable sizes produced by a rapid extrusion procedure.
1986,
Pubmed McNally,
Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds-peripherin gene.
2002,
Pubmed Molday,
Peripherin. A rim-specific membrane protein of rod outer segment discs.
1987,
Pubmed Moritz,
Fluorescent photoreceptors of transgenic Xenopus laevis imaged in vivo by two microscopy techniques.
1999,
Pubmed
,
Xenbase Moritz,
Xenopus laevis red cone opsin and Prph2 promoters allow transgene expression in amphibian cones, or both rods and cones.
2002,
Pubmed
,
Xenbase Nguyen-Legros,
Renewal of photoreceptor outer segments and their phagocytosis by the retinal pigment epithelium.
2000,
Pubmed Poetsch,
The cGMP-gated channel and related glutamic acid-rich proteins interact with peripherin-2 at the rim region of rod photoreceptor disc membranes.
2001,
Pubmed Qiao,
A specific point mutant at position 1 of the influenza hemagglutinin fusion peptide displays a hemifusion phenotype.
1999,
Pubmed Saga,
A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa.
1993,
Pubmed Sanyal,
Absence of receptor outer segments in the retina of rds mutant mice.
1981,
Pubmed Sanyal,
Development and degeneration of retina in rds mutant mice: light microscopy.
1980,
Pubmed Skehel,
Coiled coils in both intracellular vesicle and viral membrane fusion.
1998,
Pubmed Souied,
Two novel missense mutations in the peripherin/RDS gene in two unrelated French patients with autosomal dominant retinitis pigmentosa.
1998,
Pubmed Steinhauer,
Studies of the membrane fusion activities of fusion peptide mutants of influenza virus hemagglutinin.
1995,
Pubmed Struck,
Use of resonance energy transfer to monitor membrane fusion.
1981,
Pubmed Tam,
The C terminus of peripherin/rds participates in rod outer segment targeting and alignment of disk incisures.
2004,
Pubmed
,
Xenbase Tam,
Identification of an outer segment targeting signal in the COOH terminus of rhodopsin using transgenic Xenopus laevis.
2000,
Pubmed
,
Xenbase Tamm,
Membrane fusion: a structural perspective on the interplay of lipids and proteins.
2003,
Pubmed Travis,
The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.
1991,
Pubmed Travis,
Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds).
1989,
Pubmed Trujillo,
Two novel mutations (Y141H; C214Y) and previously published mutation (R142W) in the RDS-peripherin gene in autosomal dominant macular dystrophies in Spanish families.
2001,
Pubmed van Nie,
A new H-2-linked mutation, rds, causing retinal degeneration in the mouse.
1978,
Pubmed White,
Membrane fusion.
1992,
Pubmed Wrigley,
Peripherin/rds influences membrane vesicle morphology. Implications for retinopathies.
2000,
Pubmed Wu,
Raising Xenopus in the laboratory.
1991,
Pubmed
,
Xenbase Young,
Visual cells and the concept of renewal.
1976,
Pubmed Zhang,
Butterfly-shaped pattern dystrophy: a genetic, clinical, and histopathological report.
2002,
Pubmed