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Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction
The detection of light in the vertebrate retina utilizes a duplex system of closely related rod and cone photoreceptors: cones respond extremely rapidly, and operate at ‘photopic’ levels of illumination, from moonlight upwards; rods respond much more slowly, thereby obtaining greater sensitivity, an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790638/ https://www.ncbi.nlm.nih.gov/pubmed/35412676 http://dx.doi.org/10.1113/JP282058 |
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author | Lamb, Trevor D. |
author_facet | Lamb, Trevor D. |
author_sort | Lamb, Trevor D. |
collection | PubMed |
description | The detection of light in the vertebrate retina utilizes a duplex system of closely related rod and cone photoreceptors: cones respond extremely rapidly, and operate at ‘photopic’ levels of illumination, from moonlight upwards; rods respond much more slowly, thereby obtaining greater sensitivity, and function effectively only at ‘scotopic’ levels of moonlight and lower. Rods and cones employ distinct isoforms of many of the proteins in the phototransduction cascade, and they thereby represent a unique evolutionary system, whereby the same process (the detection of light) uses a distinct set of genes in two classes of cell. The molecular mechanisms of phototransduction activation are described, and the classical quantitative predictions for the onset phase of the electrical response to light are developed. Recent work predicting the recovery phase of the rod's response to intense flashes is then presented, that provides an accurate account of the time that the response spends in saturation. Importantly, this also provides a new estimate for the rate at which a single rhodopsin activates molecules of the G‐protein, transducin, that is substantially higher than other estimates in the literature. Finally, the evolutionary origin of the phototransduction proteins in rods and cones is examined, and it is shown that most of the rod/cone differences were established at the first of the two rounds of whole‐genome duplication more than 500 million years ago. |
format | Online Article Text |
id | pubmed-9790638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97906382022-12-28 Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction Lamb, Trevor D. J Physiol Article The detection of light in the vertebrate retina utilizes a duplex system of closely related rod and cone photoreceptors: cones respond extremely rapidly, and operate at ‘photopic’ levels of illumination, from moonlight upwards; rods respond much more slowly, thereby obtaining greater sensitivity, and function effectively only at ‘scotopic’ levels of moonlight and lower. Rods and cones employ distinct isoforms of many of the proteins in the phototransduction cascade, and they thereby represent a unique evolutionary system, whereby the same process (the detection of light) uses a distinct set of genes in two classes of cell. The molecular mechanisms of phototransduction activation are described, and the classical quantitative predictions for the onset phase of the electrical response to light are developed. Recent work predicting the recovery phase of the rod's response to intense flashes is then presented, that provides an accurate account of the time that the response spends in saturation. Importantly, this also provides a new estimate for the rate at which a single rhodopsin activates molecules of the G‐protein, transducin, that is substantially higher than other estimates in the literature. Finally, the evolutionary origin of the phototransduction proteins in rods and cones is examined, and it is shown that most of the rod/cone differences were established at the first of the two rounds of whole‐genome duplication more than 500 million years ago. John Wiley and Sons Inc. 2022-04-28 2022-11-01 /pmc/articles/PMC9790638/ /pubmed/35412676 http://dx.doi.org/10.1113/JP282058 Text en © 2022 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Article Lamb, Trevor D. Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
title | Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
title_full | Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
title_fullStr | Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
title_full_unstemmed | Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
title_short | Photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
title_sort | photoreceptor physiology and evolution: cellular and molecular basis of rod and cone phototransduction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790638/ https://www.ncbi.nlm.nih.gov/pubmed/35412676 http://dx.doi.org/10.1113/JP282058 |
work_keys_str_mv | AT lambtrevord photoreceptorphysiologyandevolutioncellularandmolecularbasisofrodandconephototransduction |