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Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression

Melon exhibits substantial natural variation especially in fruit ripening physiology, including both climacteric (ethylene-producing) and non-climacteric types. However, genomic mechanisms underlying such variation are not yet fully understood. Here, we report an Oxford Nanopore-based high-grade gen...

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Autores principales: Yano, Ryoichi, Ariizumi, Tohru, Nonaka, Satoko, Kawazu, Yoichi, Zhong, Silin, Mueller, Lukas, Giovannoni, James J., Rose, Jocelyn K. C., Ezura, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426833/
https://www.ncbi.nlm.nih.gov/pubmed/32792560
http://dx.doi.org/10.1038/s42003-020-01172-0
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author Yano, Ryoichi
Ariizumi, Tohru
Nonaka, Satoko
Kawazu, Yoichi
Zhong, Silin
Mueller, Lukas
Giovannoni, James J.
Rose, Jocelyn K. C.
Ezura, Hiroshi
author_facet Yano, Ryoichi
Ariizumi, Tohru
Nonaka, Satoko
Kawazu, Yoichi
Zhong, Silin
Mueller, Lukas
Giovannoni, James J.
Rose, Jocelyn K. C.
Ezura, Hiroshi
author_sort Yano, Ryoichi
collection PubMed
description Melon exhibits substantial natural variation especially in fruit ripening physiology, including both climacteric (ethylene-producing) and non-climacteric types. However, genomic mechanisms underlying such variation are not yet fully understood. Here, we report an Oxford Nanopore-based high-grade genome reference in the semi-climacteric cultivar Harukei-3 (378 Mb + 33,829 protein-coding genes), with an update of tissue-wide RNA-seq atlas in the Melonet-DB database. Comparison between Harukei-3 and DHL92, the first published melon genome, enabled identification of 24,758 one-to-one orthologue gene pairs, whereas others were candidates of copy number variation or presence/absence polymorphisms (PAPs). Further comparison based on 10 melon genome assemblies identified genome-wide PAPs of 415 retrotransposon Gag-like sequences. Of these, 160 showed fruit ripening-inducible expression, with 59.4% of the neighboring genes showing similar expression patterns (r > 0.8). Our results suggest that retrotransposons contributed to the modification of gene expression during diversification of melon genomes, and may affect fruit ripening-inducible gene expression.
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spelling pubmed-74268332020-08-18 Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression Yano, Ryoichi Ariizumi, Tohru Nonaka, Satoko Kawazu, Yoichi Zhong, Silin Mueller, Lukas Giovannoni, James J. Rose, Jocelyn K. C. Ezura, Hiroshi Commun Biol Article Melon exhibits substantial natural variation especially in fruit ripening physiology, including both climacteric (ethylene-producing) and non-climacteric types. However, genomic mechanisms underlying such variation are not yet fully understood. Here, we report an Oxford Nanopore-based high-grade genome reference in the semi-climacteric cultivar Harukei-3 (378 Mb + 33,829 protein-coding genes), with an update of tissue-wide RNA-seq atlas in the Melonet-DB database. Comparison between Harukei-3 and DHL92, the first published melon genome, enabled identification of 24,758 one-to-one orthologue gene pairs, whereas others were candidates of copy number variation or presence/absence polymorphisms (PAPs). Further comparison based on 10 melon genome assemblies identified genome-wide PAPs of 415 retrotransposon Gag-like sequences. Of these, 160 showed fruit ripening-inducible expression, with 59.4% of the neighboring genes showing similar expression patterns (r > 0.8). Our results suggest that retrotransposons contributed to the modification of gene expression during diversification of melon genomes, and may affect fruit ripening-inducible gene expression. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426833/ /pubmed/32792560 http://dx.doi.org/10.1038/s42003-020-01172-0 Text en © The Author(s) 2020 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/.
spellingShingle Article
Yano, Ryoichi
Ariizumi, Tohru
Nonaka, Satoko
Kawazu, Yoichi
Zhong, Silin
Mueller, Lukas
Giovannoni, James J.
Rose, Jocelyn K. C.
Ezura, Hiroshi
Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
title Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
title_full Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
title_fullStr Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
title_full_unstemmed Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
title_short Comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
title_sort comparative genomics of muskmelon reveals a potential role for retrotransposons in the modification of gene expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426833/
https://www.ncbi.nlm.nih.gov/pubmed/32792560
http://dx.doi.org/10.1038/s42003-020-01172-0
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