Cargando…
Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress
Calcium (Ca(2+)) is one of the essential mineral nutrients for plant growth and development. However, the effects of long-term Ca(2+) deficiency in orphan crops such as Tef [(Eragrostis tef) (Zucc.) Trotter], which accumulate high levels of Ca in the grains, remained unknown. Tef is a staple crop fo...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666473/ https://www.ncbi.nlm.nih.gov/pubmed/36380130 http://dx.doi.org/10.1038/s41598-022-23844-z |
_version_ | 1784831510923182080 |
---|---|
author | Ligaba-Osena, Ayalew Salehin, Mohammad Numan, Muhammad Wang, Xuegeng Choi, Sang-Chul Jima, Dereje Bobay, Louis-Marie Guo, Wanli |
author_facet | Ligaba-Osena, Ayalew Salehin, Mohammad Numan, Muhammad Wang, Xuegeng Choi, Sang-Chul Jima, Dereje Bobay, Louis-Marie Guo, Wanli |
author_sort | Ligaba-Osena, Ayalew |
collection | PubMed |
description | Calcium (Ca(2+)) is one of the essential mineral nutrients for plant growth and development. However, the effects of long-term Ca(2+) deficiency in orphan crops such as Tef [(Eragrostis tef) (Zucc.) Trotter], which accumulate high levels of Ca in the grains, remained unknown. Tef is a staple crop for nearly 70 million people in East Africa, particularly in Ethiopia and Eritrea. It is one of the most nutrient-dense grains, and is also more resistant to marginal soils and climatic conditions than main cereals like corn, wheat, and rice. In this study, tef plants were grown in a hydroponic solution containing optimum (1 mM) or low (0.01 mM) Ca(2+), and plant growth parameters and whole-genome transcriptome were analyzed. Ca(+2)-deficient plants exhibited leaf necrosis, leaf curling, and growth stunting symptoms. Ca(2+) deficiency significantly decreased root and shoot Ca, potassium (K), and copper content in both root and shoots. At the same time, it greatly increased root iron (Fe) content, suggesting the role of Ca(2+) in the uptake and/or translocation of these minerals. Transcriptomic analysis using RNA-seq revealed that members of Ca(2+) channels, including the cyclic nucleotide-gated channels and glutamate receptor-like channels, Ca(2+)-transporters, Ca(2+)-binding proteins and Ca(2+)-dependent protein kinases were differentially regulated by Ca(+2) treatment. Moreover, several Fe/metal transporters, including members of vacuolar Fe transporters, yellow stripe-like, natural resistance-associated macrophage protein, and oligo-peptide transporters, were differentially regulated between shoot and root in response to Ca(2+) treatment. Taken together, our findings suggest that Ca(2+) deficiency affects plant growth and mineral accumulation by regulating the transcriptomes of several transporters and signaling genes. |
format | Online Article Text |
id | pubmed-9666473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96664732022-11-17 Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress Ligaba-Osena, Ayalew Salehin, Mohammad Numan, Muhammad Wang, Xuegeng Choi, Sang-Chul Jima, Dereje Bobay, Louis-Marie Guo, Wanli Sci Rep Article Calcium (Ca(2+)) is one of the essential mineral nutrients for plant growth and development. However, the effects of long-term Ca(2+) deficiency in orphan crops such as Tef [(Eragrostis tef) (Zucc.) Trotter], which accumulate high levels of Ca in the grains, remained unknown. Tef is a staple crop for nearly 70 million people in East Africa, particularly in Ethiopia and Eritrea. It is one of the most nutrient-dense grains, and is also more resistant to marginal soils and climatic conditions than main cereals like corn, wheat, and rice. In this study, tef plants were grown in a hydroponic solution containing optimum (1 mM) or low (0.01 mM) Ca(2+), and plant growth parameters and whole-genome transcriptome were analyzed. Ca(+2)-deficient plants exhibited leaf necrosis, leaf curling, and growth stunting symptoms. Ca(2+) deficiency significantly decreased root and shoot Ca, potassium (K), and copper content in both root and shoots. At the same time, it greatly increased root iron (Fe) content, suggesting the role of Ca(2+) in the uptake and/or translocation of these minerals. Transcriptomic analysis using RNA-seq revealed that members of Ca(2+) channels, including the cyclic nucleotide-gated channels and glutamate receptor-like channels, Ca(2+)-transporters, Ca(2+)-binding proteins and Ca(2+)-dependent protein kinases were differentially regulated by Ca(+2) treatment. Moreover, several Fe/metal transporters, including members of vacuolar Fe transporters, yellow stripe-like, natural resistance-associated macrophage protein, and oligo-peptide transporters, were differentially regulated between shoot and root in response to Ca(2+) treatment. Taken together, our findings suggest that Ca(2+) deficiency affects plant growth and mineral accumulation by regulating the transcriptomes of several transporters and signaling genes. Nature Publishing Group UK 2022-11-15 /pmc/articles/PMC9666473/ /pubmed/36380130 http://dx.doi.org/10.1038/s41598-022-23844-z Text en © The Author(s) 2022 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 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/) . |
spellingShingle | Article Ligaba-Osena, Ayalew Salehin, Mohammad Numan, Muhammad Wang, Xuegeng Choi, Sang-Chul Jima, Dereje Bobay, Louis-Marie Guo, Wanli Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress |
title | Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress |
title_full | Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress |
title_fullStr | Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress |
title_full_unstemmed | Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress |
title_short | Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress |
title_sort | genome-wide transcriptome analysis of the orphan crop tef (eragrostis tef (zucc.) trotter) under long-term low calcium stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666473/ https://www.ncbi.nlm.nih.gov/pubmed/36380130 http://dx.doi.org/10.1038/s41598-022-23844-z |
work_keys_str_mv | AT ligabaosenaayalew genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT salehinmohammad genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT numanmuhammad genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT wangxuegeng genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT choisangchul genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT jimadereje genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT bobaylouismarie genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress AT guowanli genomewidetranscriptomeanalysisoftheorphancropteferagrostistefzucctrotterunderlongtermlowcalciumstress |