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Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes

Stem internodes of bioenergy sorghum inbred R.07020 are longer at high plant density (shade) than at low plant density (control). Initially, the youngest newly‐formed subapical stem internodes of shade‐treated and control plants are comparable in length. However, full‐length internodes of shade‐trea...

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Autores principales: Kebrom, Tesfamichael H., McKinley, Brian A., Mullet, John E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315773/
https://www.ncbi.nlm.nih.gov/pubmed/32607464
http://dx.doi.org/10.1002/pld3.235
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author Kebrom, Tesfamichael H.
McKinley, Brian A.
Mullet, John E.
author_facet Kebrom, Tesfamichael H.
McKinley, Brian A.
Mullet, John E.
author_sort Kebrom, Tesfamichael H.
collection PubMed
description Stem internodes of bioenergy sorghum inbred R.07020 are longer at high plant density (shade) than at low plant density (control). Initially, the youngest newly‐formed subapical stem internodes of shade‐treated and control plants are comparable in length. However, full‐length internodes of shade‐treated plants are three times longer than the internodes of the control plants. To identify the early molecular events associated with internode elongation in response to shade, we analyzed the transcriptome of the newly‐formed internodes of shade‐treated and control plants sampled between 4 and 6 hr after the start of the light period (14 hr light/10 hr dark). Sorghum genes homologous to the Arabidopsis shade marker genes ATHB2 and PIL1 were not differentially expressed. The results indicate that shade signals promote internode elongation indirectly because sorghum internodes are not illuminated and grow while enclosed with leaf sheaths. Sorghum genes homologous to the Arabidopsis morning‐phased circadian clock genes LHY, RVE, and LNK were downregulated and evening‐phased genes such as TOC1, PRR5, and GI were upregulated in young internodes in response to shade. We hypothesize that a change in the function or patterns of expression of the circadian clock genes is the earliest molecular event associated with internode elongation in response to shade in bioenergy sorghum. Increased expression of CycD1, which promotes cell division, and decreased expression of cell wall‐loosening and MBF1‐like genes, which promote cell expansion, suggest that shade signals promote internode elongation in bioenergy sorghum in part through increasing cell number by delaying transition from cell division to cell expansion.
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spelling pubmed-73157732020-06-29 Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes Kebrom, Tesfamichael H. McKinley, Brian A. Mullet, John E. Plant Direct Original Research Stem internodes of bioenergy sorghum inbred R.07020 are longer at high plant density (shade) than at low plant density (control). Initially, the youngest newly‐formed subapical stem internodes of shade‐treated and control plants are comparable in length. However, full‐length internodes of shade‐treated plants are three times longer than the internodes of the control plants. To identify the early molecular events associated with internode elongation in response to shade, we analyzed the transcriptome of the newly‐formed internodes of shade‐treated and control plants sampled between 4 and 6 hr after the start of the light period (14 hr light/10 hr dark). Sorghum genes homologous to the Arabidopsis shade marker genes ATHB2 and PIL1 were not differentially expressed. The results indicate that shade signals promote internode elongation indirectly because sorghum internodes are not illuminated and grow while enclosed with leaf sheaths. Sorghum genes homologous to the Arabidopsis morning‐phased circadian clock genes LHY, RVE, and LNK were downregulated and evening‐phased genes such as TOC1, PRR5, and GI were upregulated in young internodes in response to shade. We hypothesize that a change in the function or patterns of expression of the circadian clock genes is the earliest molecular event associated with internode elongation in response to shade in bioenergy sorghum. Increased expression of CycD1, which promotes cell division, and decreased expression of cell wall‐loosening and MBF1‐like genes, which promote cell expansion, suggest that shade signals promote internode elongation in bioenergy sorghum in part through increasing cell number by delaying transition from cell division to cell expansion. John Wiley and Sons Inc. 2020-06-25 /pmc/articles/PMC7315773/ /pubmed/32607464 http://dx.doi.org/10.1002/pld3.235 Text en © 2020 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Kebrom, Tesfamichael H.
McKinley, Brian A.
Mullet, John E.
Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
title Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
title_full Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
title_fullStr Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
title_full_unstemmed Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
title_short Shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
title_sort shade signals alter the expression of circadian clock genes in newly‐formed bioenergy sorghum internodes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315773/
https://www.ncbi.nlm.nih.gov/pubmed/32607464
http://dx.doi.org/10.1002/pld3.235
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