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Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization
The recent whole-genome duplication (WGD) in goldfish (Carassius auratus) approximately 14 million years ago makes it a valuable model for studying gene evolution during the early stages after WGD. We analyzed the transcriptome of the goldfish retina at the level of single-cell (scRNA-seq) and open...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792465/ https://www.ncbi.nlm.nih.gov/pubmed/36572749 http://dx.doi.org/10.1038/s42003-022-04351-3 |
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author | Kon, Tetsuo Fukuta, Kentaro Chen, Zelin Kon-Nanjo, Koto Suzuki, Kota Ishikawa, Masakazu Tanaka, Hikari Burgess, Shawn M. Noguchi, Hideki Toyoda, Atsushi Omori, Yoshihiro |
author_facet | Kon, Tetsuo Fukuta, Kentaro Chen, Zelin Kon-Nanjo, Koto Suzuki, Kota Ishikawa, Masakazu Tanaka, Hikari Burgess, Shawn M. Noguchi, Hideki Toyoda, Atsushi Omori, Yoshihiro |
author_sort | Kon, Tetsuo |
collection | PubMed |
description | The recent whole-genome duplication (WGD) in goldfish (Carassius auratus) approximately 14 million years ago makes it a valuable model for studying gene evolution during the early stages after WGD. We analyzed the transcriptome of the goldfish retina at the level of single-cell (scRNA-seq) and open chromatin regions (scATAC-seq). We identified a group of genes that have undergone dosage selection, accounting for 5% of the total 11,444 ohnolog pairs. We also identified 306 putative sub/neo-functionalized ohnolog pairs that are likely to be under cell-type-specific genetic variation at single-cell resolution. Diversification in the expression patterns of several ohnolog pairs was observed in the retinal cell subpopulations. The single-cell level transcriptome analysis in this study uncovered the early stages of evolution in retinal cell of goldfish after WGD. Our results provide clues for understanding the relationship between the early stages of gene evolution after WGD and the evolution of diverse vertebrate retinal functions. |
format | Online Article Text |
id | pubmed-9792465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97924652022-12-28 Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization Kon, Tetsuo Fukuta, Kentaro Chen, Zelin Kon-Nanjo, Koto Suzuki, Kota Ishikawa, Masakazu Tanaka, Hikari Burgess, Shawn M. Noguchi, Hideki Toyoda, Atsushi Omori, Yoshihiro Commun Biol Article The recent whole-genome duplication (WGD) in goldfish (Carassius auratus) approximately 14 million years ago makes it a valuable model for studying gene evolution during the early stages after WGD. We analyzed the transcriptome of the goldfish retina at the level of single-cell (scRNA-seq) and open chromatin regions (scATAC-seq). We identified a group of genes that have undergone dosage selection, accounting for 5% of the total 11,444 ohnolog pairs. We also identified 306 putative sub/neo-functionalized ohnolog pairs that are likely to be under cell-type-specific genetic variation at single-cell resolution. Diversification in the expression patterns of several ohnolog pairs was observed in the retinal cell subpopulations. The single-cell level transcriptome analysis in this study uncovered the early stages of evolution in retinal cell of goldfish after WGD. Our results provide clues for understanding the relationship between the early stages of gene evolution after WGD and the evolution of diverse vertebrate retinal functions. Nature Publishing Group UK 2022-12-26 /pmc/articles/PMC9792465/ /pubmed/36572749 http://dx.doi.org/10.1038/s42003-022-04351-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kon, Tetsuo Fukuta, Kentaro Chen, Zelin Kon-Nanjo, Koto Suzuki, Kota Ishikawa, Masakazu Tanaka, Hikari Burgess, Shawn M. Noguchi, Hideki Toyoda, Atsushi Omori, Yoshihiro Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
title | Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
title_full | Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
title_fullStr | Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
title_full_unstemmed | Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
title_short | Single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
title_sort | single-cell transcriptomics of the goldfish retina reveals genetic divergence in the asymmetrically evolved subgenomes after allotetraploidization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792465/ https://www.ncbi.nlm.nih.gov/pubmed/36572749 http://dx.doi.org/10.1038/s42003-022-04351-3 |
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