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Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development

Understanding the molecular mechanisms underlying early seed development is important in improving the grain yield and quality of crop plants. We performed a comparative label-free quantitative proteomic analysis of developing rice seeds for the WT and osctps1-2 mutant, encoding a cytidine triphosph...

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Autores principales: Yoon, Jinmi, Min, Cheol Woo, Kim, Jiyoung, Baek, Gibeom, Kim, Dohyeon, Jang, Jeong Woo, Gupta, Ravi, Kim, Sun Tae, Cho, Lae-Hyeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650807/
https://www.ncbi.nlm.nih.gov/pubmed/37960070
http://dx.doi.org/10.3390/plants12213715
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author Yoon, Jinmi
Min, Cheol Woo
Kim, Jiyoung
Baek, Gibeom
Kim, Dohyeon
Jang, Jeong Woo
Gupta, Ravi
Kim, Sun Tae
Cho, Lae-Hyeon
author_facet Yoon, Jinmi
Min, Cheol Woo
Kim, Jiyoung
Baek, Gibeom
Kim, Dohyeon
Jang, Jeong Woo
Gupta, Ravi
Kim, Sun Tae
Cho, Lae-Hyeon
author_sort Yoon, Jinmi
collection PubMed
description Understanding the molecular mechanisms underlying early seed development is important in improving the grain yield and quality of crop plants. We performed a comparative label-free quantitative proteomic analysis of developing rice seeds for the WT and osctps1-2 mutant, encoding a cytidine triphosphate synthase previously reported as the endospermless 2 (enl2) mutant in rice, harvested at 0 and 1 d after pollination (DAP) to understand the molecular mechanism of early seed development. In total, 5231 proteins were identified, of which 902 changed in abundance between 0 and 1 DAP seeds. Proteins that preferentially accumulated at 1 DAP were involved in DNA replication and pyrimidine biosynthetic pathways. Notably, an increased abundance of OsCTPS1 was observed at 1 DAP; however, no such changes were observed at the transcriptional level. We further observed that the inhibition of phosphorylation increased the stability of this protein. Furthermore, in osctps1-2, minichromosome maintenance (MCM) proteins were significantly reduced compared with those in the WT at 1 DAP, and mutations in OsMCM5 caused defects in seed development. These results highlight the molecular mechanisms underlying early seed development in rice at the post-transcriptional level.
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spelling pubmed-106508072023-10-29 Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development Yoon, Jinmi Min, Cheol Woo Kim, Jiyoung Baek, Gibeom Kim, Dohyeon Jang, Jeong Woo Gupta, Ravi Kim, Sun Tae Cho, Lae-Hyeon Plants (Basel) Article Understanding the molecular mechanisms underlying early seed development is important in improving the grain yield and quality of crop plants. We performed a comparative label-free quantitative proteomic analysis of developing rice seeds for the WT and osctps1-2 mutant, encoding a cytidine triphosphate synthase previously reported as the endospermless 2 (enl2) mutant in rice, harvested at 0 and 1 d after pollination (DAP) to understand the molecular mechanism of early seed development. In total, 5231 proteins were identified, of which 902 changed in abundance between 0 and 1 DAP seeds. Proteins that preferentially accumulated at 1 DAP were involved in DNA replication and pyrimidine biosynthetic pathways. Notably, an increased abundance of OsCTPS1 was observed at 1 DAP; however, no such changes were observed at the transcriptional level. We further observed that the inhibition of phosphorylation increased the stability of this protein. Furthermore, in osctps1-2, minichromosome maintenance (MCM) proteins were significantly reduced compared with those in the WT at 1 DAP, and mutations in OsMCM5 caused defects in seed development. These results highlight the molecular mechanisms underlying early seed development in rice at the post-transcriptional level. MDPI 2023-10-29 /pmc/articles/PMC10650807/ /pubmed/37960070 http://dx.doi.org/10.3390/plants12213715 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yoon, Jinmi
Min, Cheol Woo
Kim, Jiyoung
Baek, Gibeom
Kim, Dohyeon
Jang, Jeong Woo
Gupta, Ravi
Kim, Sun Tae
Cho, Lae-Hyeon
Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development
title Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development
title_full Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development
title_fullStr Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development
title_full_unstemmed Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development
title_short Quantitative Proteomic Analysis Deciphers the Molecular Mechanism for Endosperm Nuclear Division in Early Rice Seed Development
title_sort quantitative proteomic analysis deciphers the molecular mechanism for endosperm nuclear division in early rice seed development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650807/
https://www.ncbi.nlm.nih.gov/pubmed/37960070
http://dx.doi.org/10.3390/plants12213715
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