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A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes

PURPOSE: To present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene sequences for variations in the long wavelength-sensitive (OPN1LW), medium wavelength-sensitive (OPN1MW), short wavelength-sensitive (OPN1SW), and rhodopsin (RHO) genes. METHODS...

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Autores principales: Atilano, Shari R., Kenney, M. Cristina, Briscoe, Adriana D., Jameson, Kimberly A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058431/
https://www.ncbi.nlm.nih.gov/pubmed/32180681
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author Atilano, Shari R.
Kenney, M. Cristina
Briscoe, Adriana D.
Jameson, Kimberly A.
author_facet Atilano, Shari R.
Kenney, M. Cristina
Briscoe, Adriana D.
Jameson, Kimberly A.
author_sort Atilano, Shari R.
collection PubMed
description PURPOSE: To present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene sequences for variations in the long wavelength-sensitive (OPN1LW), medium wavelength-sensitive (OPN1MW), short wavelength-sensitive (OPN1SW), and rhodopsin (RHO) genes. METHODS: Color vision was assessed for nine subjects using the Farnsworth-Munsell 100 hue test, Ishihara pseudoisochromatic plates, and the Rabin cone-contrast threshold procedure (ColorDX, Konan Medical). The color vision phenotypes were normal trichromacy (n = 3), potential tetrachromacy (n = 3), dichromacy (n = 2), and unexplained low color vision (n = 1). DNA was isolated from blood or saliva and LR-PCR amplified into individual products: OPN1LW (4,045 bp), OPN1MW (4,045 bp), OPN1SW (3,326 bp), and RHO (6,715 bp). Each product was sequenced using specific internal primer sets. Analysis was performed with Mutation Surveyor software. RESULTS: The LR-PCR-Seq technique identified known single nucleotide polymorphisms (SNPs) in OPN1LW and OPN1MW gene codons (180, 230, 233, 277, and 285), as well as those for lesser studied codons (174, 178, 236, 274, 279, 298 and 309) in the OPN1LW and OPN1MW genes. Additionally, six SNP variants in the OPN1MW and OPN1LW genes not previously reported in the NCBI dbSNP database were identified. An unreported poly-T region within intron 5(c.36+126) of the rhodopsin gene was also found, and analysis showed it to be highly conserved in mammalian species. CONCLUSIONS: This LR-PCR-Seq procedure (single PCR reaction per gene followed by sequencing) can identify exonic and intronic SNP variants in OPN1LW, OPN1MW, OPN1SW, and rhodopsin genes. There is no need for restriction enzyme digestion or multiple PCR steps that can introduce errors. Future studies will combine the LR-PCR-Seq with perceptual behavior measures, allowing for accurate correlations between opsin genotypes, retinal photopigment phenotypes, and color perception behaviors.
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spelling pubmed-70584312020-03-16 A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes Atilano, Shari R. Kenney, M. Cristina Briscoe, Adriana D. Jameson, Kimberly A. Mol Vis Research Article PURPOSE: To present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene sequences for variations in the long wavelength-sensitive (OPN1LW), medium wavelength-sensitive (OPN1MW), short wavelength-sensitive (OPN1SW), and rhodopsin (RHO) genes. METHODS: Color vision was assessed for nine subjects using the Farnsworth-Munsell 100 hue test, Ishihara pseudoisochromatic plates, and the Rabin cone-contrast threshold procedure (ColorDX, Konan Medical). The color vision phenotypes were normal trichromacy (n = 3), potential tetrachromacy (n = 3), dichromacy (n = 2), and unexplained low color vision (n = 1). DNA was isolated from blood or saliva and LR-PCR amplified into individual products: OPN1LW (4,045 bp), OPN1MW (4,045 bp), OPN1SW (3,326 bp), and RHO (6,715 bp). Each product was sequenced using specific internal primer sets. Analysis was performed with Mutation Surveyor software. RESULTS: The LR-PCR-Seq technique identified known single nucleotide polymorphisms (SNPs) in OPN1LW and OPN1MW gene codons (180, 230, 233, 277, and 285), as well as those for lesser studied codons (174, 178, 236, 274, 279, 298 and 309) in the OPN1LW and OPN1MW genes. Additionally, six SNP variants in the OPN1MW and OPN1LW genes not previously reported in the NCBI dbSNP database were identified. An unreported poly-T region within intron 5(c.36+126) of the rhodopsin gene was also found, and analysis showed it to be highly conserved in mammalian species. CONCLUSIONS: This LR-PCR-Seq procedure (single PCR reaction per gene followed by sequencing) can identify exonic and intronic SNP variants in OPN1LW, OPN1MW, OPN1SW, and rhodopsin genes. There is no need for restriction enzyme digestion or multiple PCR steps that can introduce errors. Future studies will combine the LR-PCR-Seq with perceptual behavior measures, allowing for accurate correlations between opsin genotypes, retinal photopigment phenotypes, and color perception behaviors. Molecular Vision 2020-03-05 /pmc/articles/PMC7058431/ /pubmed/32180681 Text en Copyright © 2020 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed.
spellingShingle Research Article
Atilano, Shari R.
Kenney, M. Cristina
Briscoe, Adriana D.
Jameson, Kimberly A.
A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
title A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
title_full A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
title_fullStr A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
title_full_unstemmed A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
title_short A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
title_sort two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058431/
https://www.ncbi.nlm.nih.gov/pubmed/32180681
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