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Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus

Citrus nucellar poly-embryony (NPE) is a mode of sporophytic apomixis that asexual embryos formed in the seed through adventitious embryogenesis from the somatic nucellar cells. NPE allows clonal propagation of rootstocks, but it impedes citrus cross breeding. To understand the cellular processes in...

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Autores principales: Jia, Hui-Hui, Xu, Yuan-Tao, Yin, Zhao-Ping, Wu, Xiao-Meng, Qing, Mei, Fan, Yan-Jie, Song, Xin, Xie, Kai-Dong, Xie, Zong-Zhou, Xu, Qiang, Deng, Xiu-Xin, Guo, Wen-Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476932/
https://www.ncbi.nlm.nih.gov/pubmed/34424285
http://dx.doi.org/10.1093/dnares/dsab014
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author Jia, Hui-Hui
Xu, Yuan-Tao
Yin, Zhao-Ping
Wu, Xiao-Meng
Qing, Mei
Fan, Yan-Jie
Song, Xin
Xie, Kai-Dong
Xie, Zong-Zhou
Xu, Qiang
Deng, Xiu-Xin
Guo, Wen-Wu
author_facet Jia, Hui-Hui
Xu, Yuan-Tao
Yin, Zhao-Ping
Wu, Xiao-Meng
Qing, Mei
Fan, Yan-Jie
Song, Xin
Xie, Kai-Dong
Xie, Zong-Zhou
Xu, Qiang
Deng, Xiu-Xin
Guo, Wen-Wu
author_sort Jia, Hui-Hui
collection PubMed
description Citrus nucellar poly-embryony (NPE) is a mode of sporophytic apomixis that asexual embryos formed in the seed through adventitious embryogenesis from the somatic nucellar cells. NPE allows clonal propagation of rootstocks, but it impedes citrus cross breeding. To understand the cellular processes involved in NPE initiation, we profiled the transcriptomes and DNA methylomes in laser microdissection captured citrus apomictic cells. In apomictic cells, ribosome biogenesis and protein degradation were activated, whereas auxin polar transport was repressed. Reactive oxygen species (ROS) accumulated in the poly-embryonic ovules, and response to oxidative stress was provoked. The global DNA methylation level, especially that of CHH context, was decreased, whereas the methylation level of the NPE-controlling key gene CitRWP was increased. A C2H2 domain-containing transcription factor gene and CitRWP co-expressed specifically in apomictic cells may coordinate to initiate NPE. The activated embryogenic development and callose deposition processes indicated embryogenic fate of nucellar embryo initial (NEI) cells. In our working model for citrus NPE initiation, DNA hyper-methylation may activate transcription of CitRWP, which increases C2H2 expression and ROS accumulation, triggers epigenetic regulation and regulates cell fate transition and NEI cell identity in the apomictic cells.
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spelling pubmed-84769322021-09-29 Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus Jia, Hui-Hui Xu, Yuan-Tao Yin, Zhao-Ping Wu, Xiao-Meng Qing, Mei Fan, Yan-Jie Song, Xin Xie, Kai-Dong Xie, Zong-Zhou Xu, Qiang Deng, Xiu-Xin Guo, Wen-Wu DNA Res Research Article Citrus nucellar poly-embryony (NPE) is a mode of sporophytic apomixis that asexual embryos formed in the seed through adventitious embryogenesis from the somatic nucellar cells. NPE allows clonal propagation of rootstocks, but it impedes citrus cross breeding. To understand the cellular processes involved in NPE initiation, we profiled the transcriptomes and DNA methylomes in laser microdissection captured citrus apomictic cells. In apomictic cells, ribosome biogenesis and protein degradation were activated, whereas auxin polar transport was repressed. Reactive oxygen species (ROS) accumulated in the poly-embryonic ovules, and response to oxidative stress was provoked. The global DNA methylation level, especially that of CHH context, was decreased, whereas the methylation level of the NPE-controlling key gene CitRWP was increased. A C2H2 domain-containing transcription factor gene and CitRWP co-expressed specifically in apomictic cells may coordinate to initiate NPE. The activated embryogenic development and callose deposition processes indicated embryogenic fate of nucellar embryo initial (NEI) cells. In our working model for citrus NPE initiation, DNA hyper-methylation may activate transcription of CitRWP, which increases C2H2 expression and ROS accumulation, triggers epigenetic regulation and regulates cell fate transition and NEI cell identity in the apomictic cells. Oxford University Press 2021-08-23 /pmc/articles/PMC8476932/ /pubmed/34424285 http://dx.doi.org/10.1093/dnares/dsab014 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Jia, Hui-Hui
Xu, Yuan-Tao
Yin, Zhao-Ping
Wu, Xiao-Meng
Qing, Mei
Fan, Yan-Jie
Song, Xin
Xie, Kai-Dong
Xie, Zong-Zhou
Xu, Qiang
Deng, Xiu-Xin
Guo, Wen-Wu
Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
title Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
title_full Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
title_fullStr Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
title_full_unstemmed Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
title_short Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
title_sort transcriptomes and dna methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476932/
https://www.ncbi.nlm.nih.gov/pubmed/34424285
http://dx.doi.org/10.1093/dnares/dsab014
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