Evidence map›Paper›PMID 15252042›Full record

ArticleThe Journal of biological chemistry2004

Uncoupling of photoreceptor peripherin/rds fusogenic activity from biosynthesis, subunit assembly, and targeting: a potential mechanism for pathogenic effects.

Linda M Ritter, Kathleen Boesze-Battaglia, Beatrice M Tam, Orson L Moritz, Nidhi Khattree, Shu-Chu Chen, Andrew F X Goldberg

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Molecular basis for photoreceptor outer segment architecture.Progress in retinal and eye research · 2016
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Linda M RitterEye Research Institute, Oakland University, Rochester, Michigan 48309, USA.
Kathleen Boesze-Battaglia
Beatrice M Tam
Orson L Moritz
Nidhi Khattree
Shu-Chu Chen
Andrew F X Goldberg
Smith-Kettlewell Eye Research Institute · USUniversity of British Columbia · CAOakland University · USUniversity of Pennsylvania · US

Funding

MEMBRANE FUSION IN RETINAL ROD OUTER SEGMENTSR01EY010420 · NEI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI BOESZE-BATTAGLIA, KATHLEEN · 1999 to 2016
$4.7M
PERIPHERIN/RDS IN PHOTORECEPTOR RENEWAL AND DISEASER01EY013246 · NEI · OAKLAND UNIVERSITY · PI GOLDBERG, ANDREW FX · 2001 to 2014
$3.5M
Vision Research Infrastructure Development Grant (R24)R24EY014803 · NEI · OAKLAND UNIVERSITY · PI GIBLIN, FRANK JOSEPH · 2003 to 2007
$1.1M
Nikon A1R confocal laser microscope system for live cell imagingS10RR026365 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI BOESZE-BATTAGLIA, KATHLEEN · 2010 to 2010
$500k
A Role for Melanoregulin in RPE-mediated PhagocytosisR21EY018705 · NEI · UNIVERSITY OF PENNSYLVANIA · PI BOESZE-BATTAGLIA, KATHLEEN · 2009 to 2010
$437k
MEMBRANE FUSION IN RETINAL ROD OUTER SEGMENTSR29EY010420 · NEI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI BOESZE-BATTAGLIA, KATHLEEN B · 1994 to 1998
–
NCRR NIH HHS S10 RR026365NEI NIH HHS EY014803NEI NIH HHS EY10420NEI NIH HHS EY13246NEI NIH HHS R01 EY010420NEI NIH HHS R01 EY013246NEI NIH HHS R21 EY018705NEI NIH HHS R24 EY014803NEI NIH HHS R29 EY010420
6 · The paper itself

Abstract

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.

Indexed as

Amino Acid SequenceAnimalsAnimals, Genetically ModifiedCell MembraneCOS CellsDisulfidesEscherichia coliFluorescent Antibody TechniqueGlutathione TransferaseIntermediate Filament ProteinsMembrane GlycoproteinsMolecular Sequence DataMutagenesisNerve Tissue ProteinsPeripherinsRecombinant Fusion ProteinsDisulfidesGlutathione TransferaseIntermediate Filament ProteinsMembrane GlycoproteinsNerve Tissue ProteinsPeripherinsPRPH2 protein, humanPRPH protein, humanPRPH protein, XenopusRecombinant Fusion ProteinsXenopus Proteins

Identifiers

PMID15252042
PMCPMC1360210
OpenAlexW2058917275

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.