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Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation

BACKGROUND: Maize is one of the primary crops of genetic manipulation, which provides an excellent means of promoting stress resistance and increasing yield. However, the differences in induction and regeneration capacity of embryonic callus (EC) among various genotypes result in genotypic dependenc...

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Autores principales: Zhang, Xiaoling, Wang, Yanli, Yan, Yuanyuan, Peng, Hua, Long, Yun, Zhang, Yinchao, Jiang, Zhou, Liu, Peng, Zou, Chaoying, Peng, Huanwei, Pan, Guangtang, Shen, Yaou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391841/
https://www.ncbi.nlm.nih.gov/pubmed/30813896
http://dx.doi.org/10.1186/s12864-019-5506-7
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author Zhang, Xiaoling
Wang, Yanli
Yan, Yuanyuan
Peng, Hua
Long, Yun
Zhang, Yinchao
Jiang, Zhou
Liu, Peng
Zou, Chaoying
Peng, Huanwei
Pan, Guangtang
Shen, Yaou
author_facet Zhang, Xiaoling
Wang, Yanli
Yan, Yuanyuan
Peng, Hua
Long, Yun
Zhang, Yinchao
Jiang, Zhou
Liu, Peng
Zou, Chaoying
Peng, Huanwei
Pan, Guangtang
Shen, Yaou
author_sort Zhang, Xiaoling
collection PubMed
description BACKGROUND: Maize is one of the primary crops of genetic manipulation, which provides an excellent means of promoting stress resistance and increasing yield. However, the differences in induction and regeneration capacity of embryonic callus (EC) among various genotypes result in genotypic dependence in genetic transformation. RESULTS: In this study, embryonic calli of two maize inbred lines with strong redifferentiation capacity and two lines with weak redifferentiation capability were separately subjected to transcriptome sequencing analysis during the early redifferentiation stages (stage I, 1–3 d; stage II, 4–6 d; stage III, 7–9 d) along with their corresponding controls. A total of ~ 654.72 million cDNA clean reads were yielded, and 62.64%~ 69.21% clean reads were mapped to the reference genome for each library. In comparison with the control, the numbers of differentially expressed genes (DEGs) for the four inbred lines identified in the three stages ranged from 1694 to 7193. By analyzing the common and specific DEGs of the four materials, we found that there were 321 upregulated genes and 386 downregulated genes identified in the high-regeneration lines (141 and DH40), whereas 611 upregulated genes and 500 downregulated genes were specifically expressed in the low-regeneration lines (ZYDH381–1 and DH3732). Analysis of the DEG expression patterns indicated a sharp change at stage I in both the high- and low-regeneration lines, which suggested that stage I constitutes a crucial period for EC regeneration. Notably, the specific common DEGs of 141 and DH40 were mainly associated with photosynthesis, porphyrin and chlorophyll metabolism, ribosomes, and plant hormone signal transduction. In contrast, the DEGs in ZYDH381–1 and DH3732 were mainly related to taurine and hypotaurine metabolism, nitrogen metabolism, fatty acid elongation, starch and sucrose metabolism, phenylpropanoid biosynthesis, and plant circadian rhythm. More importantly, WOX genes, which have an ancestral role in embryo development in seed plants and promote the regeneration of transformed calli, were specifically upregulated in the two high-regeneration lines. CONCLUSIONS: Our research contributes to the elucidation of molecular regulation during early redifferentiation in the maize embryonic callus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5506-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63918412019-03-11 Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation Zhang, Xiaoling Wang, Yanli Yan, Yuanyuan Peng, Hua Long, Yun Zhang, Yinchao Jiang, Zhou Liu, Peng Zou, Chaoying Peng, Huanwei Pan, Guangtang Shen, Yaou BMC Genomics Research Article BACKGROUND: Maize is one of the primary crops of genetic manipulation, which provides an excellent means of promoting stress resistance and increasing yield. However, the differences in induction and regeneration capacity of embryonic callus (EC) among various genotypes result in genotypic dependence in genetic transformation. RESULTS: In this study, embryonic calli of two maize inbred lines with strong redifferentiation capacity and two lines with weak redifferentiation capability were separately subjected to transcriptome sequencing analysis during the early redifferentiation stages (stage I, 1–3 d; stage II, 4–6 d; stage III, 7–9 d) along with their corresponding controls. A total of ~ 654.72 million cDNA clean reads were yielded, and 62.64%~ 69.21% clean reads were mapped to the reference genome for each library. In comparison with the control, the numbers of differentially expressed genes (DEGs) for the four inbred lines identified in the three stages ranged from 1694 to 7193. By analyzing the common and specific DEGs of the four materials, we found that there were 321 upregulated genes and 386 downregulated genes identified in the high-regeneration lines (141 and DH40), whereas 611 upregulated genes and 500 downregulated genes were specifically expressed in the low-regeneration lines (ZYDH381–1 and DH3732). Analysis of the DEG expression patterns indicated a sharp change at stage I in both the high- and low-regeneration lines, which suggested that stage I constitutes a crucial period for EC regeneration. Notably, the specific common DEGs of 141 and DH40 were mainly associated with photosynthesis, porphyrin and chlorophyll metabolism, ribosomes, and plant hormone signal transduction. In contrast, the DEGs in ZYDH381–1 and DH3732 were mainly related to taurine and hypotaurine metabolism, nitrogen metabolism, fatty acid elongation, starch and sucrose metabolism, phenylpropanoid biosynthesis, and plant circadian rhythm. More importantly, WOX genes, which have an ancestral role in embryo development in seed plants and promote the regeneration of transformed calli, were specifically upregulated in the two high-regeneration lines. CONCLUSIONS: Our research contributes to the elucidation of molecular regulation during early redifferentiation in the maize embryonic callus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5506-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-27 /pmc/articles/PMC6391841/ /pubmed/30813896 http://dx.doi.org/10.1186/s12864-019-5506-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Xiaoling
Wang, Yanli
Yan, Yuanyuan
Peng, Hua
Long, Yun
Zhang, Yinchao
Jiang, Zhou
Liu, Peng
Zou, Chaoying
Peng, Huanwei
Pan, Guangtang
Shen, Yaou
Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
title Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
title_full Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
title_fullStr Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
title_full_unstemmed Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
title_short Transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
title_sort transcriptome sequencing analysis of maize embryonic callus during early redifferentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391841/
https://www.ncbi.nlm.nih.gov/pubmed/30813896
http://dx.doi.org/10.1186/s12864-019-5506-7
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