Cargando…
Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives
BACKGROUND: Tripsacum dactyloides (2n = 4x = 72) and Zea perennis (2n = 4x = 40) are tertiary gene pools of Zea mays L. and exhibit many abiotic adaptations absent in modern maize, especially salt tolerance. A previously reported allopolyploid (hereafter referred to as MTP, 2n = 74) synthesized usin...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887930/ https://www.ncbi.nlm.nih.gov/pubmed/36717785 http://dx.doi.org/10.1186/s12864-023-09148-0 |
_version_ | 1784880439541891072 |
---|---|
author | Li, Xiaofeng Wang, Xingyu Ma, Qiangqiang Zhong, Yunfeng Zhang, Yibo Zhang, Ping Li, Yingzheng He, Ruyu Zhou, Yang Li, Yang Cheng, Mingjun Yan, Xu Li, Yan He, Jianmei Iqbal, Muhammad Zafar Rong, Tingzhao Tang, Qilin |
author_facet | Li, Xiaofeng Wang, Xingyu Ma, Qiangqiang Zhong, Yunfeng Zhang, Yibo Zhang, Ping Li, Yingzheng He, Ruyu Zhou, Yang Li, Yang Cheng, Mingjun Yan, Xu Li, Yan He, Jianmei Iqbal, Muhammad Zafar Rong, Tingzhao Tang, Qilin |
author_sort | Li, Xiaofeng |
collection | PubMed |
description | BACKGROUND: Tripsacum dactyloides (2n = 4x = 72) and Zea perennis (2n = 4x = 40) are tertiary gene pools of Zea mays L. and exhibit many abiotic adaptations absent in modern maize, especially salt tolerance. A previously reported allopolyploid (hereafter referred to as MTP, 2n = 74) synthesized using Zea mays, Tripsacum dactyloides, and Zea perennis has even stronger salt tolerance than Z. perennis and T. dactyloides. This allopolyploid will be a powerful genetic bridge for the genetic improvement of maize. However, the molecular mechanisms underlying its salt tolerance, as well as the key genes involved in regulating its salt tolerance, remain unclear. RESULTS: Single-molecule real-time sequencing and RNA sequencing were used to identify the genes involved in salt tolerance and reveal the underlying molecular mechanisms. Based on the SMRT-seq results, we obtained 227,375 reference unigenes with an average length of 2300 bp; most of the unigenes were annotated to Z. mays sequences (76.5%) in the NR database. Moreover, a total of 484 and 1053 differentially expressed genes (DEGs) were identified in the leaves and roots, respectively. Functional enrichment analysis of DEGs revealed that multiple pathways responded to salt stress, including “Flavonoid biosynthesis,” “Oxidoreductase activity,” and “Plant hormone signal transduction” in the leaves and roots, and “Iron ion binding,” “Acetyl-CoA carboxylase activity,” and “Serine-type carboxypeptidase activity” in the roots. Transcription factors, such as those in the WRKY, B3-ARF, and bHLH families, and cytokinin negatively regulators negatively regulated the salt stress response. According to the results of the short time series-expression miner analysis, proteins involved in “Spliceosome” and “MAPK signal pathway” dynamically responded to salt stress as salinity changed. Protein–protein interaction analysis revealed that heat shock proteins play a role in the large interaction network regulating salt tolerance. CONCLUSIONS: Our results reveal the molecular mechanism underlying the regulation of MTP in the response to salt stress and abundant salt-tolerance-related unigenes. These findings will aid the retrieval of lost alleles in modern maize and provide a new approach for using T. dactyloides and Z. perennis to improve maize. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09148-0. |
format | Online Article Text |
id | pubmed-9887930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98879302023-02-01 Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives Li, Xiaofeng Wang, Xingyu Ma, Qiangqiang Zhong, Yunfeng Zhang, Yibo Zhang, Ping Li, Yingzheng He, Ruyu Zhou, Yang Li, Yang Cheng, Mingjun Yan, Xu Li, Yan He, Jianmei Iqbal, Muhammad Zafar Rong, Tingzhao Tang, Qilin BMC Genomics Research BACKGROUND: Tripsacum dactyloides (2n = 4x = 72) and Zea perennis (2n = 4x = 40) are tertiary gene pools of Zea mays L. and exhibit many abiotic adaptations absent in modern maize, especially salt tolerance. A previously reported allopolyploid (hereafter referred to as MTP, 2n = 74) synthesized using Zea mays, Tripsacum dactyloides, and Zea perennis has even stronger salt tolerance than Z. perennis and T. dactyloides. This allopolyploid will be a powerful genetic bridge for the genetic improvement of maize. However, the molecular mechanisms underlying its salt tolerance, as well as the key genes involved in regulating its salt tolerance, remain unclear. RESULTS: Single-molecule real-time sequencing and RNA sequencing were used to identify the genes involved in salt tolerance and reveal the underlying molecular mechanisms. Based on the SMRT-seq results, we obtained 227,375 reference unigenes with an average length of 2300 bp; most of the unigenes were annotated to Z. mays sequences (76.5%) in the NR database. Moreover, a total of 484 and 1053 differentially expressed genes (DEGs) were identified in the leaves and roots, respectively. Functional enrichment analysis of DEGs revealed that multiple pathways responded to salt stress, including “Flavonoid biosynthesis,” “Oxidoreductase activity,” and “Plant hormone signal transduction” in the leaves and roots, and “Iron ion binding,” “Acetyl-CoA carboxylase activity,” and “Serine-type carboxypeptidase activity” in the roots. Transcription factors, such as those in the WRKY, B3-ARF, and bHLH families, and cytokinin negatively regulators negatively regulated the salt stress response. According to the results of the short time series-expression miner analysis, proteins involved in “Spliceosome” and “MAPK signal pathway” dynamically responded to salt stress as salinity changed. Protein–protein interaction analysis revealed that heat shock proteins play a role in the large interaction network regulating salt tolerance. CONCLUSIONS: Our results reveal the molecular mechanism underlying the regulation of MTP in the response to salt stress and abundant salt-tolerance-related unigenes. These findings will aid the retrieval of lost alleles in modern maize and provide a new approach for using T. dactyloides and Z. perennis to improve maize. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09148-0. BioMed Central 2023-01-31 /pmc/articles/PMC9887930/ /pubmed/36717785 http://dx.doi.org/10.1186/s12864-023-09148-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Li, Xiaofeng Wang, Xingyu Ma, Qiangqiang Zhong, Yunfeng Zhang, Yibo Zhang, Ping Li, Yingzheng He, Ruyu Zhou, Yang Li, Yang Cheng, Mingjun Yan, Xu Li, Yan He, Jianmei Iqbal, Muhammad Zafar Rong, Tingzhao Tang, Qilin Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
title | Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
title_full | Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
title_fullStr | Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
title_full_unstemmed | Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
title_short | Integrated single-molecule real-time sequencing and RNA sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
title_sort | integrated single-molecule real-time sequencing and rna sequencing reveal the molecular mechanisms of salt tolerance in a novel synthesized polyploid genetic bridge between maize and its wild relatives |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887930/ https://www.ncbi.nlm.nih.gov/pubmed/36717785 http://dx.doi.org/10.1186/s12864-023-09148-0 |
work_keys_str_mv | AT lixiaofeng integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT wangxingyu integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT maqiangqiang integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT zhongyunfeng integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT zhangyibo integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT zhangping integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT liyingzheng integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT heruyu integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT zhouyang integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT liyang integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT chengmingjun integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT yanxu integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT liyan integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT hejianmei integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT iqbalmuhammadzafar integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT rongtingzhao integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives AT tangqilin integratedsinglemoleculerealtimesequencingandrnasequencingrevealthemolecularmechanismsofsalttoleranceinanovelsynthesizedpolyploidgeneticbridgebetweenmaizeanditswildrelatives |