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Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening

Heat Stress Factor A9 (A9), a seed-specific transcription factor contributing to seed longevity, also enhances phytochrome-dependent seedling greening. The RNA-seq analyses of imbibed-seed transcripts here reported indicated potential additional effects of A9 on cryptochrome-mediated blue-light resp...

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Autores principales: Almoguera, Concepción, Prieto-Dapena, Pilar, Carranco, Raúl, Ruiz, José Luis, Jordano, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154816/
https://www.ncbi.nlm.nih.gov/pubmed/32155706
http://dx.doi.org/10.3390/plants9030335
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author Almoguera, Concepción
Prieto-Dapena, Pilar
Carranco, Raúl
Ruiz, José Luis
Jordano, Juan
author_facet Almoguera, Concepción
Prieto-Dapena, Pilar
Carranco, Raúl
Ruiz, José Luis
Jordano, Juan
author_sort Almoguera, Concepción
collection PubMed
description Heat Stress Factor A9 (A9), a seed-specific transcription factor contributing to seed longevity, also enhances phytochrome-dependent seedling greening. The RNA-seq analyses of imbibed-seed transcripts here reported indicated potential additional effects of A9 on cryptochrome-mediated blue-light responses. These analyses also suggested that in contrast to the A9 effects on longevity, which require coactivation by additional factors as A4a, A9 alone might suffice for the enhancement of photomorphogenesis at the seedling stage. We found that upon its seed-specific overexpression, A9 indeed enhanced the expected blue-light responses. Comparative loss-of-function analyses of longevity and greening, performed by similar expression of dominant-negative and inactive forms of A9, not only confirmed the additional greening effects of A9, but also were consistent with A9 not requiring A4a (or additional factors) for the greening effects. Our results strongly indicate that A9 would differentially regulate seed longevity and photomorphogenesis at the seedling stage, A9 alone sufficing for both the phytochrome- and cryptochrome-dependent greening enhancement effects.
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spelling pubmed-71548162020-04-21 Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening Almoguera, Concepción Prieto-Dapena, Pilar Carranco, Raúl Ruiz, José Luis Jordano, Juan Plants (Basel) Article Heat Stress Factor A9 (A9), a seed-specific transcription factor contributing to seed longevity, also enhances phytochrome-dependent seedling greening. The RNA-seq analyses of imbibed-seed transcripts here reported indicated potential additional effects of A9 on cryptochrome-mediated blue-light responses. These analyses also suggested that in contrast to the A9 effects on longevity, which require coactivation by additional factors as A4a, A9 alone might suffice for the enhancement of photomorphogenesis at the seedling stage. We found that upon its seed-specific overexpression, A9 indeed enhanced the expected blue-light responses. Comparative loss-of-function analyses of longevity and greening, performed by similar expression of dominant-negative and inactive forms of A9, not only confirmed the additional greening effects of A9, but also were consistent with A9 not requiring A4a (or additional factors) for the greening effects. Our results strongly indicate that A9 would differentially regulate seed longevity and photomorphogenesis at the seedling stage, A9 alone sufficing for both the phytochrome- and cryptochrome-dependent greening enhancement effects. MDPI 2020-03-06 /pmc/articles/PMC7154816/ /pubmed/32155706 http://dx.doi.org/10.3390/plants9030335 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
Almoguera, Concepción
Prieto-Dapena, Pilar
Carranco, Raúl
Ruiz, José Luis
Jordano, Juan
Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening
title Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening
title_full Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening
title_fullStr Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening
title_full_unstemmed Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening
title_short Heat Stress Factors Expressed during Seed Maturation Differentially Regulate Seed Longevity and Seedling Greening
title_sort heat stress factors expressed during seed maturation differentially regulate seed longevity and seedling greening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154816/
https://www.ncbi.nlm.nih.gov/pubmed/32155706
http://dx.doi.org/10.3390/plants9030335
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