Evidence map›Paper›PMID 30514708›Full record

ArticleGenetics2019

Coupling of Human Rhodopsin to a Yeast Signaling Pathway Enables Characterization of Mutations Associated with Retinal Disease.

Benjamin M Scott, Steven K Chen, Nihar Bhattacharyya, Abdiwahab Y Moalim, Sergey V Plotnikov, Elise Heon, Sergio G Peisajovich, Belinda S W Chang

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Screening of Chemical Libraries Using a Yeast Model of Retinal Disease.SLAS discovery : advancing life sciences R & D · 2019
    Article
  10. Article
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

8 authors at 2 institutions in 1 country.

Benjamin M ScottDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada.
Steven K ChenDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada.
Nihar BhattacharyyaDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada.
Abdiwahab Y MoalimDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada.
Sergey V PlotnikovDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada.
Elise HeonDepartment of Ophthalmology, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.
Sergio G PeisajovichDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada.
Belinda S W ChangDepartment of Cell and Systems Biology, University of Toronto, Ontario M5S 3G5, Canada belinda.chang@utoronto.ca.ORCID 0000-0002-6525-4429
University of Toronto · CAHospital for Sick Children · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are crucial sensors of extracellular signals in eukaryotes, with multiple GPCR mutations linked to human diseases. With the growing number of sequenced human genomes, determining the pathogenicity of a mutation is challenging, but can be aided by a direct measurement of GPCR-mediated signaling. This is particularly difficult for the visual pigment rhodopsin-a GPCR activated by light-for which hundreds of mutations have been linked to inherited degenerative retinal diseases such as retinitis pigmentosa. In this study, we successfully engineered, for the first time, activation by human rhodopsin of the yeast mating pathway, resulting in signaling via a fluorescent reporter. We combine this novel assay for rhodopsin light-dependent activation with studies of subcellular localization, and the upregulation of the unfolded protein response in response to misfolded rhodopsin protein. We use these assays to characterize a panel of rhodopsin mutations with known molecular phenotypes, finding that rhodopsin maintains a similar molecular phenotype in yeast, with some interesting differences. Furthermore, we compare our assays in yeast with clinical phenotypes from patients with novel disease-linked mutations. We demonstrate that our engineered yeast strain can be useful in rhodopsin mutant classification, and in helping to determine the molecular mechanisms underlying their pathogenicity. This approach may also be applied to better understand the clinical relevance of other human GPCR mutations, furthering the use of yeast as a tool for investigating molecular mechanisms relevant to human disease.

Indexed as

Mutation, MissenseSignal TransductionCell Line, TumorGenes, Mating Type, FungalHumansRetinitis PigmentosaRhodopsinSaccharomyces cerevisiaeRhodopsindisease modelG protein-coupled receptorretinitis pigmentosarhodopsinVisual degenerative disease

Identifiers

PMID30514708
PMCPMC6366926
OpenAlexW2902881290

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.