Cargando…

Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores

Stress-induced microspore embryogenesis is a widely employed method to achieve homozygosity in plant breeding programs. However, the molecular mechanisms that govern gametophyte de- and redifferentiation are understood poorly. In this study, RNA-Seq was used to evaluate global changes across the mic...

Descripción completa

Detalles Bibliográficos
Autores principales: Hale, Brett, Phipps, Callie, Rao, Naina, Wijeratne, Asela, Phillips, Gregory C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695151/
https://www.ncbi.nlm.nih.gov/pubmed/33171842
http://dx.doi.org/10.3390/plants9111510
_version_ 1783615124345454592
author Hale, Brett
Phipps, Callie
Rao, Naina
Wijeratne, Asela
Phillips, Gregory C.
author_facet Hale, Brett
Phipps, Callie
Rao, Naina
Wijeratne, Asela
Phillips, Gregory C.
author_sort Hale, Brett
collection PubMed
description Stress-induced microspore embryogenesis is a widely employed method to achieve homozygosity in plant breeding programs. However, the molecular mechanisms that govern gametophyte de- and redifferentiation are understood poorly. In this study, RNA-Seq was used to evaluate global changes across the microspore transcriptome of soybean (Glycine max [L.] Merrill) as a consequence of pretreatment low-temperature stress. Expression analysis revealed more than 20,000 differentially expressed genes between treated and control microspore populations. Functional enrichment illustrated that many of these genes (e.g., those encoding heat shock proteins and cytochrome P450s) were upregulated to maintain cellular homeostasis through the mitigation of oxidative damage. Moreover, transcripts corresponding to saccharide metabolism, vacuolar transport, and other pollen-related developmental processes were drastically downregulated among treated microspores. Temperature stress also triggered cell wall modification and cell proliferation—characteristics that implied putative commitment to an embryonic pathway. These findings collectively demonstrate that pretreatment cold stress induces soybean microspore reprogramming through suppression of the gametophytic program while concomitantly driving sporophytic development.
format Online
Article
Text
id pubmed-7695151
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-76951512020-11-28 Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores Hale, Brett Phipps, Callie Rao, Naina Wijeratne, Asela Phillips, Gregory C. Plants (Basel) Article Stress-induced microspore embryogenesis is a widely employed method to achieve homozygosity in plant breeding programs. However, the molecular mechanisms that govern gametophyte de- and redifferentiation are understood poorly. In this study, RNA-Seq was used to evaluate global changes across the microspore transcriptome of soybean (Glycine max [L.] Merrill) as a consequence of pretreatment low-temperature stress. Expression analysis revealed more than 20,000 differentially expressed genes between treated and control microspore populations. Functional enrichment illustrated that many of these genes (e.g., those encoding heat shock proteins and cytochrome P450s) were upregulated to maintain cellular homeostasis through the mitigation of oxidative damage. Moreover, transcripts corresponding to saccharide metabolism, vacuolar transport, and other pollen-related developmental processes were drastically downregulated among treated microspores. Temperature stress also triggered cell wall modification and cell proliferation—characteristics that implied putative commitment to an embryonic pathway. These findings collectively demonstrate that pretreatment cold stress induces soybean microspore reprogramming through suppression of the gametophytic program while concomitantly driving sporophytic development. MDPI 2020-11-07 /pmc/articles/PMC7695151/ /pubmed/33171842 http://dx.doi.org/10.3390/plants9111510 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hale, Brett
Phipps, Callie
Rao, Naina
Wijeratne, Asela
Phillips, Gregory C.
Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores
title Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores
title_full Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores
title_fullStr Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores
title_full_unstemmed Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores
title_short Differential Expression Profiling Reveals Stress-Induced Cell Fate Divergence in Soybean Microspores
title_sort differential expression profiling reveals stress-induced cell fate divergence in soybean microspores
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695151/
https://www.ncbi.nlm.nih.gov/pubmed/33171842
http://dx.doi.org/10.3390/plants9111510
work_keys_str_mv AT halebrett differentialexpressionprofilingrevealsstressinducedcellfatedivergenceinsoybeanmicrospores
AT phippscallie differentialexpressionprofilingrevealsstressinducedcellfatedivergenceinsoybeanmicrospores
AT raonaina differentialexpressionprofilingrevealsstressinducedcellfatedivergenceinsoybeanmicrospores
AT wijeratneasela differentialexpressionprofilingrevealsstressinducedcellfatedivergenceinsoybeanmicrospores
AT phillipsgregoryc differentialexpressionprofilingrevealsstressinducedcellfatedivergenceinsoybeanmicrospores