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Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology
BACKGROUND: Tillering is a complicated process in plant and is a significant trait that affects biomass and seed yield of bunch grass Psathyrostachys juncea, a typical perennial forage species. To clarify the regulatory mechanisms of tillering in P. juncea and to explore related candidate genes coul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502641/ https://www.ncbi.nlm.nih.gov/pubmed/36151542 http://dx.doi.org/10.1186/s12870-022-03837-w |
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author | Li, Zhen Yun, Lan Ren, Xiaomin Shi, Fengling Mi, Fugui |
author_facet | Li, Zhen Yun, Lan Ren, Xiaomin Shi, Fengling Mi, Fugui |
author_sort | Li, Zhen |
collection | PubMed |
description | BACKGROUND: Tillering is a complicated process in plant and is a significant trait that affects biomass and seed yield of bunch grass Psathyrostachys juncea, a typical perennial forage species. To clarify the regulatory mechanisms of tillering in P. juncea and to explore related candidate genes could be helpful to improve the seed and forage yield of perennial gramineous forages. We selected the tiller node tissues of P. juncea for transcriptome sequencing to determine the differentially expressed genes (DEG) between dense and sparse tillering genotypes. The metabolic pathway was studied, candidate genes were screened, and reference genes stability were evaluated. RESULTS: The results showed that approximately 5466 DEGs were identified between the two genotypes with dense and sparse tillers of P. juncea, which significantly differed in tiller number. Tillering regulation pathways analysis suggested that DEGs closely related to the biosynthesis of three plant hormones, namely auxin (IAA), cytokinin (CTK), and strigolactones (SLs), while “biosynthesis of lignin” and “nitrogen metabolism” have remarkable differences between the dense and sparse tillering genotypes. Meanwhile, the reference gene Actin1, having the best stability, was screened from twelve genes with highest expression level and was used in verification of ten tillering related candidate genes. CONCLUSIONS: The tillering mechanism of perennial grass P. juncea was expounded by transcriptome analysis of tiller node tissues. We demonstrated that dense-tillering genotypes may be distinguished by their low expression patterns of genes involved in SL, IAA, and high expression patterns of genes involved in CTK biosynthesis at the tillering stage, and nitrogen metabolism and lignin biosynthesis can also affect the number of tillers. Furthermore, the expression level of ten tillering related candidate genes were verified using Actin1 as reference gene. These candidate genes provide valuable breeding resources for marker assisted selection and yield traits improvement of P. juncea. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03837-w. |
format | Online Article Text |
id | pubmed-9502641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95026412022-09-24 Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology Li, Zhen Yun, Lan Ren, Xiaomin Shi, Fengling Mi, Fugui BMC Plant Biol Research BACKGROUND: Tillering is a complicated process in plant and is a significant trait that affects biomass and seed yield of bunch grass Psathyrostachys juncea, a typical perennial forage species. To clarify the regulatory mechanisms of tillering in P. juncea and to explore related candidate genes could be helpful to improve the seed and forage yield of perennial gramineous forages. We selected the tiller node tissues of P. juncea for transcriptome sequencing to determine the differentially expressed genes (DEG) between dense and sparse tillering genotypes. The metabolic pathway was studied, candidate genes were screened, and reference genes stability were evaluated. RESULTS: The results showed that approximately 5466 DEGs were identified between the two genotypes with dense and sparse tillers of P. juncea, which significantly differed in tiller number. Tillering regulation pathways analysis suggested that DEGs closely related to the biosynthesis of three plant hormones, namely auxin (IAA), cytokinin (CTK), and strigolactones (SLs), while “biosynthesis of lignin” and “nitrogen metabolism” have remarkable differences between the dense and sparse tillering genotypes. Meanwhile, the reference gene Actin1, having the best stability, was screened from twelve genes with highest expression level and was used in verification of ten tillering related candidate genes. CONCLUSIONS: The tillering mechanism of perennial grass P. juncea was expounded by transcriptome analysis of tiller node tissues. We demonstrated that dense-tillering genotypes may be distinguished by their low expression patterns of genes involved in SL, IAA, and high expression patterns of genes involved in CTK biosynthesis at the tillering stage, and nitrogen metabolism and lignin biosynthesis can also affect the number of tillers. Furthermore, the expression level of ten tillering related candidate genes were verified using Actin1 as reference gene. These candidate genes provide valuable breeding resources for marker assisted selection and yield traits improvement of P. juncea. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03837-w. BioMed Central 2022-09-23 /pmc/articles/PMC9502641/ /pubmed/36151542 http://dx.doi.org/10.1186/s12870-022-03837-w Text en © The Author(s) 2022 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, Zhen Yun, Lan Ren, Xiaomin Shi, Fengling Mi, Fugui Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology |
title | Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology |
title_full | Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology |
title_fullStr | Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology |
title_full_unstemmed | Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology |
title_short | Analysis of controlling genes for tiller growth of Psathyrostachys juncea based on transcriptome sequencing technology |
title_sort | analysis of controlling genes for tiller growth of psathyrostachys juncea based on transcriptome sequencing technology |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502641/ https://www.ncbi.nlm.nih.gov/pubmed/36151542 http://dx.doi.org/10.1186/s12870-022-03837-w |
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