Evidence map›Paper›PMID 27353443›Full record

ArticleThe Journal of general physiology2016

Rhodopsin kinase and arrestin binding control the decay of photoactivated rhodopsin and dark adaptation of mouse rods.

Rikard Frederiksen, Soile Nymark, Alexander V Kolesnikov, Justin D Berry, Leopold Adler, Yiannis Koutalos, Vladimir J Kefalov, M Carter Cornwall

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. E122Q rhodopsin: pigment microspectrophotometry, photoreceptor light responses, and bleaching adaptation.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2026
    Article
  2. Article
  3. The physiology of dark adaptation: Progress and future directions.Progress in retinal and eye research · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Rod Photoreceptors Avoid Saturation in Bright Light by the Movement of the G Protein Transducin.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  14. Article
  15. Article
  16. Shedding new light on the generation of the visual chromophore.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Review
  17. Phosphorylation at Serine 21 in G protein-coupled receptor kinase 1 (GRK1) is required for normal kinetics of dark adaption in rod but not cone photoreceptors.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  18. Photic generation of 11-The Journal of biological chemistry · 2019
    Article
  19. Article
  20. Elementary response triggered by transducin in retinal rods.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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 3 institutions in 2 countries.

Rikard FrederiksenDepartment of Physiology and Biophysics, Boston University School of Medicine, Boston, MA 02118 rikardf@bu.edu.
Soile NymarkDepartment of Electronics and Communications Engineering, BioMediTech, Tampere University of Technology, 33720 Tampere, Finland.
Alexander V KolesnikovDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110.
Justin D BerryDepartment of Physiology and Biophysics, Boston University School of Medicine, Boston, MA 02118.
Leopold AdlerDepartment of Ophthalmology, Medical University of South Carolina, Charleston, SC 29425.
Yiannis KoutalosDepartment of Ophthalmology, Medical University of South Carolina, Charleston, SC 29425.
Vladimir J KefalovDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110.
M Carter CornwallDepartment of Physiology and Biophysics, Boston University School of Medicine, Boston, MA 02118.
Boston University · USMedical University of South Carolina · USTampere University · FI

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Philip Andrew Ruzycki · 1985 to 2026
$18.4M
Pharmacological Treatment of Retinal DiseasesR24EY021126 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI PALCZEWSKI, KRZYSZTOF · 2010 to 2014
$12.8M
Spectral & Metabolic Basis of Visual ResponsesR01EY001157 · NEI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CORNWALL, M CARTER · 1985 to 2020
$8.3M
Transport Processes in PhotoreceptorsR01EY014850 · NEI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KOUTALOS, YIANNIS · 2004 to 2022
$5.3M
MECHANISMS OF ADAPTATION IN MAMMALIAN CONESR01EY019312 · NEI · WASHINGTON UNIVERSITY · PI KEFALOV, VLADIMIR JIVKOV · 2009 to 2017
$3.3M
PIGMENT DEPHOSPHORYLATION IN MAMMALIAN ROD AND CONE PHOTORECEPTORSR01EY025696 · NEI · WASHINGTON UNIVERSITY · PI KEFALOV, VLADIMIR JIVKOV · 2016 to 2019
$1.5M
NEI NIH HHS P30 EY002687NEI NIH HHS R01 EY001157NEI NIH HHS R01 EY014850NEI NIH HHS R01 EY019312NEI NIH HHS R01 EY025696NEI NIH HHS R24 EY021126
6 · The paper itself

Abstract

Photoactivation of vertebrate rhodopsin converts it to the physiologically active Meta II (R*) state, which triggers the rod light response. Meta II is rapidly inactivated by the phosphorylation of C-terminal serine and threonine residues by G-protein receptor kinase (Grk1) and subsequent binding of arrestin 1 (Arr1). Meta II exists in equilibrium with the more stable inactive form of rhodopsin, Meta III. Dark adaptation of rods requires the complete thermal decay of Meta II/Meta III into opsin and all-trans retinal and the subsequent regeneration of rhodopsin with 11-cis retinal chromophore. In this study, we examine the regulation of Meta III decay by Grk1 and Arr1 in intact mouse rods and their effect on rod dark adaptation. We measure the rates of Meta III decay in isolated retinas of wild-type (WT), Grk1-deficient (Grk1(-/-)), Arr1-deficient (Arr1(-/-)), and Arr1-overexpressing (Arr1(ox)) mice. We find that in WT mouse rods, Meta III peaks ∼6 min after rhodopsin activation and decays with a time constant (τ) of 17 min. Meta III decay slows in Arr1(-/-) rods (τ of ∼27 min), whereas it accelerates in Arr1(ox) rods (τ of ∼8 min) and Grk1(-/-) rods (τ of ∼13 min). In all cases, regeneration of rhodopsin with exogenous 11-cis retinal is rate limited by the decay of Meta III. Notably, the kinetics of rod dark adaptation in vivo is also modulated by the levels of Arr1 and Grk1. We conclude that, in addition to their well-established roles in Meta II inactivation, Grk1 and Arr1 can modulate the kinetics of Meta III decay and rod dark adaptation in vivo.

Indexed as

AnimalsArrestinsDark AdaptationG-Protein-Coupled Receptor Kinase 1MiceMice, KnockoutPhosphorylationPhotic StimulationProtein BindingRetinal Rod Photoreceptor CellsRhodopsinarrestin 1 protein, mouseArrestinsG-Protein-Coupled Receptor Kinase 1Grk1 protein, mouseRhodopsin

Identifiers

PMID27353443
PMCPMC4924931
OpenAlexW2468509568

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.