Literature DB >> 35091503

Reproducibility of the Rod Photoreceptor Response Depends Critically on the Concentration of the Phosphodiesterase Effector Enzyme.

Ala Morshedian1, Gabriela Sendek1, Sze Yin Ng1, Kimberly Boyd2, Roxana A Radu1, Mingyao Liu3, Nikolai O Artemyev2, Alapakkam P Sampath1, Gordon L Fain4,5.   

Abstract

The high sensitivity of night vision requires that rod photoreceptors reliably and reproducibly signal the absorption of single photons, a process that depends on tight regulation of intracellular cGMP concentration through the phototransduction cascade. Here in the mouse (Mus musculus), we studied a single-site D167A mutation of the gene for the α subunit of rod photoreceptor phosphodiesterase (PDEA), made with the aim of removing a noncatalytic binding site for cGMP. This mutation unexpectedly eliminated nearly all PDEA expression and reduced expression of the β subunit (PDEB) to ∼5%-10% of WT. The remaining PDE had nearly normal specific activity; degeneration was slow, with 50%-60% of rods remaining after 6 months. Responses were larger and more sensitive than normal but slower in rise and decay, probably from slower dark turnover of cGMP. Remarkably, responses became much less reproducible than WT, with response variance increasing for amplitude by over 10-fold, and for latency and time-to-peak by >100-fold. We hypothesize that the increase in variance is the result of greater variability in the dark-resting concentration of cGMP, produced by spatial and temporal nonuniformity in spontaneous PDE activity. This variability decreased as stimuli were made brighter, presumably because of greater spatial uniformity of phototransduction and the approach to saturation. We conclude that the constancy of the rod response depends critically on PDE expression to maintain adequate spontaneous PDE activity, so that the concentration of second messenger is relatively uniform throughout the outer segment.SIGNIFICANCE STATEMENT Rod photoreceptors in the vertebrate retina reliably signal the absorption of single photons of light by generating responses that are remarkably reproducible in amplitude and waveform. We show that this reproducibility depends critically on the concentration of the effector enzyme phosphodiesterase (PDE), which metabolizes the second messenger cGMP and generates rod light responses. In rods with the D167A mutation of the α subunit of PDE, only 5%-10% of PDE is expressed. Single-photon responses then become much more variable than in WT rods. We think this variability is caused by spatial and temporal inhomogeneity in the concentration of cGMP in darkness, so that photons absorbed in different parts of the cell produce responses of greatly varying amplitude and waveform.
Copyright © 2022 the authors.

Entities:  

Keywords:  GAF A domain; phosphodiesterase; rod photoreceptor; sensitivity; single-photon response; transduction

Mesh:

Substances:

Year:  2022        PMID: 35091503      PMCID: PMC8936574          DOI: 10.1523/JNEUROSCI.2119-21.2021

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.709


  40 in total

1.  Responses of retinal rods to single photons.

Authors:  D A Baylor; T D Lamb; K W Yau
Journal:  J Physiol       Date:  1979-03       Impact factor: 5.182

2.  cGMP binding sites on photoreceptor phosphodiesterase: role in feedback regulation of visual transduction.

Authors:  R H Cote; M D Bownds; V Y Arshavsky
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

3.  How rods respond to single photons: Key adaptations of a G-protein cascade that enable vision at the physical limit of perception.

Authors:  Jürgen Reingruber; David Holcman; Gordon L Fain
Journal:  Bioessays       Date:  2015-09-10       Impact factor: 4.345

4.  Onset of feedback reactions underlying vertebrate rod photoreceptor light adaptation.

Authors:  P D Calvert; T W Ho; Y M LeFebvre; V Y Arshavsky
Journal:  J Gen Physiol       Date:  1998-01       Impact factor: 4.086

5.  Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1.

Authors:  C K Chen; M E Burns; W He; T G Wensel; D A Baylor; M I Simon
Journal:  Nature       Date:  2000-02-03       Impact factor: 49.962

6.  Rhodopsin phosphorylation as a mechanism of cyclic GMP phosphodiesterase regulation by S-modulin.

Authors:  S Kawamura
Journal:  Nature       Date:  1993-04-29       Impact factor: 49.962

7.  Highly cooperative feedback control of retinal rod guanylate cyclase by calcium ions.

Authors:  K W Koch; L Stryer
Journal:  Nature       Date:  1988-07-07       Impact factor: 49.962

Review 8.  New focus on regulation of the rod photoreceptor phosphodiesterase.

Authors:  Sahil Gulati; Krzysztof Palczewski
Journal:  Curr Opin Struct Biol       Date:  2021-05-01       Impact factor: 7.786

9.  Cryo-EM structure of phosphodiesterase 6 reveals insights into the allosteric regulation of type I phosphodiesterases.

Authors:  Sahil Gulati; Krzysztof Palczewski; Andreas Engel; Henning Stahlberg; Lubomir Kovacik
Journal:  Sci Adv       Date:  2019-02-27       Impact factor: 14.136

10.  Exchange of Cone for Rod Phosphodiesterase 6 Catalytic Subunits in Rod Photoreceptors Mimics in Part Features of Light Adaptation.

Authors:  Anurima Majumder; Johan Pahlberg; Hakim Muradov; Kimberly K Boyd; Alapakkam P Sampath; Nikolai O Artemyev
Journal:  J Neurosci       Date:  2015-06-17       Impact factor: 6.167

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