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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-10650807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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