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Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars

Comparative transcriptomics can be used to translate an understanding of gene regulatory networks from model systems to less studied species. Here, we use RNA-Seq to determine and compare gene expression dynamics through the floral transition in the model species Arabidopsis thaliana and the closely...

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Autores principales: Calderwood, Alexander, Hepworth, Jo, Woodhouse, Shannon, Bilham, Lorelei, Jones, D. Marc, Tudor, Eleri, Ali, Mubarak, Dean, Caroline, Wells, Rachel, Irwin, Judith A., Morris, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095958/
https://www.ncbi.nlm.nih.gov/pubmed/37077206
http://dx.doi.org/10.1017/qpb.2021.6
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author Calderwood, Alexander
Hepworth, Jo
Woodhouse, Shannon
Bilham, Lorelei
Jones, D. Marc
Tudor, Eleri
Ali, Mubarak
Dean, Caroline
Wells, Rachel
Irwin, Judith A.
Morris, Richard J.
author_facet Calderwood, Alexander
Hepworth, Jo
Woodhouse, Shannon
Bilham, Lorelei
Jones, D. Marc
Tudor, Eleri
Ali, Mubarak
Dean, Caroline
Wells, Rachel
Irwin, Judith A.
Morris, Richard J.
author_sort Calderwood, Alexander
collection PubMed
description Comparative transcriptomics can be used to translate an understanding of gene regulatory networks from model systems to less studied species. Here, we use RNA-Seq to determine and compare gene expression dynamics through the floral transition in the model species Arabidopsis thaliana and the closely related crop Brassica rapa. We find that different curve registration functions are required for different genes, indicating that there is no single common ‘developmental time’ between Arabidopsis and B. rapa. A detailed comparison between Arabidopsis and B. rapa and between two B. rapa accessions reveals different modes of regulation of the key floral integrator SOC1, and that the floral transition in the B. rapa accessions is triggered by different pathways. Our study adds to the mechanistic understanding of the regulatory network of flowering time in rapid cycling B. rapa and highlights the importance of registration methods for the comparison of developmental gene expression data.
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spelling pubmed-100959582023-04-18 Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars Calderwood, Alexander Hepworth, Jo Woodhouse, Shannon Bilham, Lorelei Jones, D. Marc Tudor, Eleri Ali, Mubarak Dean, Caroline Wells, Rachel Irwin, Judith A. Morris, Richard J. Quant Plant Biol Original Research Article Comparative transcriptomics can be used to translate an understanding of gene regulatory networks from model systems to less studied species. Here, we use RNA-Seq to determine and compare gene expression dynamics through the floral transition in the model species Arabidopsis thaliana and the closely related crop Brassica rapa. We find that different curve registration functions are required for different genes, indicating that there is no single common ‘developmental time’ between Arabidopsis and B. rapa. A detailed comparison between Arabidopsis and B. rapa and between two B. rapa accessions reveals different modes of regulation of the key floral integrator SOC1, and that the floral transition in the B. rapa accessions is triggered by different pathways. Our study adds to the mechanistic understanding of the regulatory network of flowering time in rapid cycling B. rapa and highlights the importance of registration methods for the comparison of developmental gene expression data. Cambridge University Press 2021-04-26 /pmc/articles/PMC10095958/ /pubmed/37077206 http://dx.doi.org/10.1017/qpb.2021.6 Text en © The Author(s), 2021. Published by Cambridge University Press in association with The John Innes Centre 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Calderwood, Alexander
Hepworth, Jo
Woodhouse, Shannon
Bilham, Lorelei
Jones, D. Marc
Tudor, Eleri
Ali, Mubarak
Dean, Caroline
Wells, Rachel
Irwin, Judith A.
Morris, Richard J.
Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars
title Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars
title_full Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars
title_fullStr Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars
title_full_unstemmed Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars
title_short Comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between Arabidopsis and Brassica rapa cultivars
title_sort comparative transcriptomics reveals desynchronisation of gene expression during the floral transition between arabidopsis and brassica rapa cultivars
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095958/
https://www.ncbi.nlm.nih.gov/pubmed/37077206
http://dx.doi.org/10.1017/qpb.2021.6
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