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Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa

BACKGROUND: Night-break (NB) has been proven to repress flowering of short-day plants (SDPs). Long-noncoding RNAs (lncRNAs) play key roles in plant flowering. However, investigation of the relationship between lncRNAs and NB responses is still limited, especially in Chenopodium quinoa, an important...

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Autores principales: Wu, Qi, Luo, Yiming, Wu, Xiaoyong, Bai, Xue, Ye, Xueling, Liu, Changying, Wan, Yan, Xiang, Dabing, Li, Qiang, Zou, Liang, Zhao, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056640/
https://www.ncbi.nlm.nih.gov/pubmed/33874907
http://dx.doi.org/10.1186/s12864-021-07605-2
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author Wu, Qi
Luo, Yiming
Wu, Xiaoyong
Bai, Xue
Ye, Xueling
Liu, Changying
Wan, Yan
Xiang, Dabing
Li, Qiang
Zou, Liang
Zhao, Gang
author_facet Wu, Qi
Luo, Yiming
Wu, Xiaoyong
Bai, Xue
Ye, Xueling
Liu, Changying
Wan, Yan
Xiang, Dabing
Li, Qiang
Zou, Liang
Zhao, Gang
author_sort Wu, Qi
collection PubMed
description BACKGROUND: Night-break (NB) has been proven to repress flowering of short-day plants (SDPs). Long-noncoding RNAs (lncRNAs) play key roles in plant flowering. However, investigation of the relationship between lncRNAs and NB responses is still limited, especially in Chenopodium quinoa, an important short-day coarse cereal. RESULTS: In this study, we performed strand-specific RNA-seq of leaf samples collected from quinoa seedlings treated by SD and NB. A total of 4914 high-confidence lncRNAs were identified, out of which 91 lncRNAs showed specific responses to SD and NB. Based on the expression profiles, we identified 17 positive- and 7 negative-flowering lncRNAs. Co-expression network analysis indicated that 1653 mRNAs were the common targets of both types of flowering lncRNAs. By mapping these targets to the known flowering pathways in model plants, we found some pivotal flowering homologs, including 2 florigen encoding genes (FT (FLOWERING LOCUS T) and TSF (TWIN SISTER of FT) homologs), 3 circadian clock related genes (EARLY FLOWERING 3 (ELF3), LATE ELONGATED HYPOCOTYL (LHY) and ELONGATED HYPOCOTYL 5 (HY5) homologs), 2 photoreceptor genes (PHYTOCHROME A (PHYA) and CRYPTOCHROME1 (CRY1) homologs), 1 B-BOX type CONSTANS (CO) homolog and 1 RELATED TO ABI3/VP1 (RAV1) homolog, were specifically affected by NB and competed by the positive and negative-flowering lncRNAs. We speculated that these potential flowering lncRNAs may mediate quinoa NB responses by modifying the expression of the floral homologous genes. CONCLUSIONS: Together, the findings in this study will deepen our understanding of the roles of lncRNAs in NB responses, and provide valuable information for functional characterization in future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07605-2.
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spelling pubmed-80566402021-04-20 Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa Wu, Qi Luo, Yiming Wu, Xiaoyong Bai, Xue Ye, Xueling Liu, Changying Wan, Yan Xiang, Dabing Li, Qiang Zou, Liang Zhao, Gang BMC Genomics Research BACKGROUND: Night-break (NB) has been proven to repress flowering of short-day plants (SDPs). Long-noncoding RNAs (lncRNAs) play key roles in plant flowering. However, investigation of the relationship between lncRNAs and NB responses is still limited, especially in Chenopodium quinoa, an important short-day coarse cereal. RESULTS: In this study, we performed strand-specific RNA-seq of leaf samples collected from quinoa seedlings treated by SD and NB. A total of 4914 high-confidence lncRNAs were identified, out of which 91 lncRNAs showed specific responses to SD and NB. Based on the expression profiles, we identified 17 positive- and 7 negative-flowering lncRNAs. Co-expression network analysis indicated that 1653 mRNAs were the common targets of both types of flowering lncRNAs. By mapping these targets to the known flowering pathways in model plants, we found some pivotal flowering homologs, including 2 florigen encoding genes (FT (FLOWERING LOCUS T) and TSF (TWIN SISTER of FT) homologs), 3 circadian clock related genes (EARLY FLOWERING 3 (ELF3), LATE ELONGATED HYPOCOTYL (LHY) and ELONGATED HYPOCOTYL 5 (HY5) homologs), 2 photoreceptor genes (PHYTOCHROME A (PHYA) and CRYPTOCHROME1 (CRY1) homologs), 1 B-BOX type CONSTANS (CO) homolog and 1 RELATED TO ABI3/VP1 (RAV1) homolog, were specifically affected by NB and competed by the positive and negative-flowering lncRNAs. We speculated that these potential flowering lncRNAs may mediate quinoa NB responses by modifying the expression of the floral homologous genes. CONCLUSIONS: Together, the findings in this study will deepen our understanding of the roles of lncRNAs in NB responses, and provide valuable information for functional characterization in future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07605-2. BioMed Central 2021-04-19 /pmc/articles/PMC8056640/ /pubmed/33874907 http://dx.doi.org/10.1186/s12864-021-07605-2 Text en © The Author(s) 2021 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
Wu, Qi
Luo, Yiming
Wu, Xiaoyong
Bai, Xue
Ye, Xueling
Liu, Changying
Wan, Yan
Xiang, Dabing
Li, Qiang
Zou, Liang
Zhao, Gang
Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa
title Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa
title_full Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa
title_fullStr Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa
title_full_unstemmed Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa
title_short Identification of the specific long-noncoding RNAs involved in night-break mediated flowering retardation in Chenopodium quinoa
title_sort identification of the specific long-noncoding rnas involved in night-break mediated flowering retardation in chenopodium quinoa
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056640/
https://www.ncbi.nlm.nih.gov/pubmed/33874907
http://dx.doi.org/10.1186/s12864-021-07605-2
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