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Uncovering transcriptional reprogramming during callus development in soybean: insights and implications

Callus, a valuable tool in plant genetic engineering, originates from dedifferentiated cells. While transcriptional reprogramming during callus formation has been extensively studied in Arabidopsis thaliana, our knowledge of this process in other species, such as Glycine max, remains limited. To bri...

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Autores principales: Park, Joo-Seok, Choi, Yoram, Jeong, Min-Gyun, Jeong, Yeong-Il, Han, Ji-Hyun, Choi, Hong-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436568/
https://www.ncbi.nlm.nih.gov/pubmed/37600197
http://dx.doi.org/10.3389/fpls.2023.1239917
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author Park, Joo-Seok
Choi, Yoram
Jeong, Min-Gyun
Jeong, Yeong-Il
Han, Ji-Hyun
Choi, Hong-Kyu
author_facet Park, Joo-Seok
Choi, Yoram
Jeong, Min-Gyun
Jeong, Yeong-Il
Han, Ji-Hyun
Choi, Hong-Kyu
author_sort Park, Joo-Seok
collection PubMed
description Callus, a valuable tool in plant genetic engineering, originates from dedifferentiated cells. While transcriptional reprogramming during callus formation has been extensively studied in Arabidopsis thaliana, our knowledge of this process in other species, such as Glycine max, remains limited. To bridge this gap, our study focused on conducting a time-series transcriptome analysis of soybean callus cultured for various durations (0, 1, 7, 14, 28, and 42 days) on a callus induction medium following wounding with the attempt of identifying genes that play key roles during callus formation. As the result, we detected a total of 27,639 alterations in gene expression during callus formation, which could be categorized into eight distinct clusters. Gene ontology analysis revealed that genes associated with hormones, cell wall modification, and cell cycle underwent transcriptional reprogramming throughout callus formation. Furthermore, by scrutinizing the expression patterns of genes related to hormones, cell cycle, cell wall, and transcription factors, we discovered that auxin, cytokinin, and brassinosteroid signaling pathways activate genes involved in both root and shoot meristem development during callus formation. In summary, our transcriptome analysis provides significant insights into the molecular mechanisms governing callus formation in soybean. The information obtained from this study contributes to a deeper understanding of this intricate process and paves the way for further investigation in the field.
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spelling pubmed-104365682023-08-19 Uncovering transcriptional reprogramming during callus development in soybean: insights and implications Park, Joo-Seok Choi, Yoram Jeong, Min-Gyun Jeong, Yeong-Il Han, Ji-Hyun Choi, Hong-Kyu Front Plant Sci Plant Science Callus, a valuable tool in plant genetic engineering, originates from dedifferentiated cells. While transcriptional reprogramming during callus formation has been extensively studied in Arabidopsis thaliana, our knowledge of this process in other species, such as Glycine max, remains limited. To bridge this gap, our study focused on conducting a time-series transcriptome analysis of soybean callus cultured for various durations (0, 1, 7, 14, 28, and 42 days) on a callus induction medium following wounding with the attempt of identifying genes that play key roles during callus formation. As the result, we detected a total of 27,639 alterations in gene expression during callus formation, which could be categorized into eight distinct clusters. Gene ontology analysis revealed that genes associated with hormones, cell wall modification, and cell cycle underwent transcriptional reprogramming throughout callus formation. Furthermore, by scrutinizing the expression patterns of genes related to hormones, cell cycle, cell wall, and transcription factors, we discovered that auxin, cytokinin, and brassinosteroid signaling pathways activate genes involved in both root and shoot meristem development during callus formation. In summary, our transcriptome analysis provides significant insights into the molecular mechanisms governing callus formation in soybean. The information obtained from this study contributes to a deeper understanding of this intricate process and paves the way for further investigation in the field. Frontiers Media S.A. 2023-08-04 /pmc/articles/PMC10436568/ /pubmed/37600197 http://dx.doi.org/10.3389/fpls.2023.1239917 Text en Copyright © 2023 Park, Choi, Jeong, Jeong, Han and Choi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Park, Joo-Seok
Choi, Yoram
Jeong, Min-Gyun
Jeong, Yeong-Il
Han, Ji-Hyun
Choi, Hong-Kyu
Uncovering transcriptional reprogramming during callus development in soybean: insights and implications
title Uncovering transcriptional reprogramming during callus development in soybean: insights and implications
title_full Uncovering transcriptional reprogramming during callus development in soybean: insights and implications
title_fullStr Uncovering transcriptional reprogramming during callus development in soybean: insights and implications
title_full_unstemmed Uncovering transcriptional reprogramming during callus development in soybean: insights and implications
title_short Uncovering transcriptional reprogramming during callus development in soybean: insights and implications
title_sort uncovering transcriptional reprogramming during callus development in soybean: insights and implications
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436568/
https://www.ncbi.nlm.nih.gov/pubmed/37600197
http://dx.doi.org/10.3389/fpls.2023.1239917
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