Cargando…

Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato

To identify cytoplasmic male sterility (CMS)-associated genes in tomato, we determined the genome sequences of mitochondria and chloroplasts in three CMS tomato lines derived from independent asymmetric cell fusions, their nuclear and cytoplasmic donors, and male fertile weedy cultivated tomato and...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuwabara, Kosuke, Harada, Issei, Matsuzawa, Yuma, Ariizumi, Tohru, Shirasawa, Kenta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632925/
https://www.ncbi.nlm.nih.gov/pubmed/34848681
http://dx.doi.org/10.1038/s41438-021-00676-y
_version_ 1784607846657163264
author Kuwabara, Kosuke
Harada, Issei
Matsuzawa, Yuma
Ariizumi, Tohru
Shirasawa, Kenta
author_facet Kuwabara, Kosuke
Harada, Issei
Matsuzawa, Yuma
Ariizumi, Tohru
Shirasawa, Kenta
author_sort Kuwabara, Kosuke
collection PubMed
description To identify cytoplasmic male sterility (CMS)-associated genes in tomato, we determined the genome sequences of mitochondria and chloroplasts in three CMS tomato lines derived from independent asymmetric cell fusions, their nuclear and cytoplasmic donors, and male fertile weedy cultivated tomato and wild relatives. The structures of the CMS mitochondrial genomes were highly divergent from those of the nuclear and cytoplasmic donors, and genes of the donors were mixed up in these genomes. On the other hand, the structures of CMS chloroplast genomes were moderately conserved across the donors, but CMS chloroplast genes were unexpectedly likely derived from the nuclear donors. Comparative analysis of the structures and contents of organelle genes and transcriptome analysis identified three genes that were uniquely present in the CMS lines, but not in the donor or fertile lines. RNA-sequencing analysis indicated that these three genes transcriptionally expressed in anther, and identified different RNA editing levels in one gene, orf265, that was partially similar to ATP synthase subunit 8, between fertile and sterile lines. The orf265 was a highly potential candidate for CMS-associated gene. This study suggests that organelle reorganization mechanisms after cell fusion events differ between mitochondria and chloroplasts, and provides insight into the development of new F1 hybrid breeding programs employing the CMS system in tomato.
format Online
Article
Text
id pubmed-8632925
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-86329252021-12-01 Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato Kuwabara, Kosuke Harada, Issei Matsuzawa, Yuma Ariizumi, Tohru Shirasawa, Kenta Hortic Res Article To identify cytoplasmic male sterility (CMS)-associated genes in tomato, we determined the genome sequences of mitochondria and chloroplasts in three CMS tomato lines derived from independent asymmetric cell fusions, their nuclear and cytoplasmic donors, and male fertile weedy cultivated tomato and wild relatives. The structures of the CMS mitochondrial genomes were highly divergent from those of the nuclear and cytoplasmic donors, and genes of the donors were mixed up in these genomes. On the other hand, the structures of CMS chloroplast genomes were moderately conserved across the donors, but CMS chloroplast genes were unexpectedly likely derived from the nuclear donors. Comparative analysis of the structures and contents of organelle genes and transcriptome analysis identified three genes that were uniquely present in the CMS lines, but not in the donor or fertile lines. RNA-sequencing analysis indicated that these three genes transcriptionally expressed in anther, and identified different RNA editing levels in one gene, orf265, that was partially similar to ATP synthase subunit 8, between fertile and sterile lines. The orf265 was a highly potential candidate for CMS-associated gene. This study suggests that organelle reorganization mechanisms after cell fusion events differ between mitochondria and chloroplasts, and provides insight into the development of new F1 hybrid breeding programs employing the CMS system in tomato. Nature Publishing Group UK 2021-12-01 /pmc/articles/PMC8632925/ /pubmed/34848681 http://dx.doi.org/10.1038/s41438-021-00676-y Text en © The Author(s) 2021 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
Kuwabara, Kosuke
Harada, Issei
Matsuzawa, Yuma
Ariizumi, Tohru
Shirasawa, Kenta
Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
title Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
title_full Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
title_fullStr Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
title_full_unstemmed Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
title_short Organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
title_sort organelle genome assembly uncovers the dynamic genome reorganization and cytoplasmic male sterility associated genes in tomato
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632925/
https://www.ncbi.nlm.nih.gov/pubmed/34848681
http://dx.doi.org/10.1038/s41438-021-00676-y
work_keys_str_mv AT kuwabarakosuke organellegenomeassemblyuncoversthedynamicgenomereorganizationandcytoplasmicmalesterilityassociatedgenesintomato
AT haradaissei organellegenomeassemblyuncoversthedynamicgenomereorganizationandcytoplasmicmalesterilityassociatedgenesintomato
AT matsuzawayuma organellegenomeassemblyuncoversthedynamicgenomereorganizationandcytoplasmicmalesterilityassociatedgenesintomato
AT ariizumitohru organellegenomeassemblyuncoversthedynamicgenomereorganizationandcytoplasmicmalesterilityassociatedgenesintomato
AT shirasawakenta organellegenomeassemblyuncoversthedynamicgenomereorganizationandcytoplasmicmalesterilityassociatedgenesintomato