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黄花羽扇豆花朵、花柄和豆荚的转录组分析揭示了器官脱落过程中的复杂表达变化。

Transcriptome Profiling of Flowers, Flower Pedicels and Pods of (Yellow Lupine) Reveals Complex Expression Changes during Organ Abscission.

作者信息

Glazinska Paulina, Wojciechowski Waldemar, Kulasek Milena, Glinkowski Wojciech, Marciniak Katarzyna, Klajn Natalia, Kesy Jacek, Kopcewicz Jan

机构信息

Department of Biology and Environmental Science, Nicolaus Copernicus UniversityTorun, Poland.

Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus UniversityTorun, Poland.

出版信息

Front Plant Sci. 2017 May 2;8:641. doi: 10.3389/fpls.2017.00641. eCollection 2017.

DOI:10.3389/fpls.2017.00641
PMID:28512462
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5412092/
Abstract

Yellow lupine ( L., Taper c.), a member of the legume family ( L.), has an enormous practical importance. Its excessive flower and pod abscission represents an economic drawback, as proper flower and seed formation and development is crucial for the plant's productivity. Generative organ detachment takes place at the basis of the pedicels, within a specialized group of cells collectively known as the abscission zone (AZ). During plant growth these cells become competent to respond to specific signals that trigger separation and lead to the abolition of cell wall adhesion. Little is known about the molecular network controlling the yellow lupine organ abscission. The aim of our study was to establish the divergences and similarities in transcriptional networks in the pods, flowers and flower pedicels abscised or maintained on the plant, and to identify genes playing key roles in generative organ abscission in yellow lupine. Based on transcriptome assembly, we identified 166,473 unigenes representing 219,514 assembled unique transcripts from flowers, flower pedicels and pods undergoing abscission and from control organs. Comparison of the cDNA libraries from dropped and control organs helped in identifying 1,343, 2,933 and 1,491 differentially expressed genes (DEGs) in the flowers, flower pedicels and pods, respectively. In DEG analyses, we focused on genes involved in phytohormonal regulation, cell wall functioning and metabolic pathways. Our results indicate that auxin, ethylene and gibberellins are some of the main factors engaged in generative organ abscission. Identified 28 DEGs common for all library comparisons are involved in cell wall functioning, protein metabolism, water homeostasis and stress response. Interestingly, among the common DEGs we also found an miR169 precursor, which is the first evidence of micro RNA engaged in abscission. A KEGG pathway enrichment analysis revealed that the identified DEGs were predominantly involved in carbohydrate and amino acid metabolism, but some other pathways were also targeted. This study represents the first comprehensive transcriptome-based characterization of organ abscission in and provides a valuable data source not only for understanding the abscission signaling pathway in yellow lupine, but also for further research aimed at improving crop yields.

摘要

黄花羽扇豆(L., Taper c.)是豆科(L.)的一员,具有巨大的实际重要性。其过多的花和荚脱落是一个经济缺陷,因为适当的花和种子形成与发育对植物的生产力至关重要。生殖器官的脱落发生在花梗基部,在一组统称为脱落区(AZ)的特化细胞内。在植物生长过程中,这些细胞能够响应特定信号,触发分离并导致细胞壁粘附的消除。关于控制黄花羽扇豆器官脱落的分子网络知之甚少。我们研究的目的是确定在植物上脱落或保留的豆荚、花和花梗转录网络中的差异和相似性,并鉴定在黄花羽扇豆生殖器官脱落中起关键作用的基因。基于转录组组装,我们从正在脱落的花、花梗和豆荚以及对照器官中鉴定出166,473个单基因,代表219,514个组装的独特转录本。比较脱落器官和对照器官的cDNA文库有助于分别鉴定花、花梗和豆荚中1,343、2,933和1,491个差异表达基因(DEG)。在DEG分析中,我们关注参与植物激素调节、细胞壁功能和代谢途径的基因。我们的结果表明,生长素、乙烯和赤霉素是参与生殖器官脱落的一些主要因素。在所有文库比较中鉴定出的28个共同DEG参与细胞壁功能、蛋白质代谢、水平衡和应激反应。有趣的是,在共同的DEG中我们还发现了一个miR169前体,这是参与脱落的 microRNA 的首个证据。KEGG 通路富集分析表明,鉴定出的DEG主要参与碳水化合物和氨基酸代谢,但也针对其他一些通路。这项研究代表了对黄花羽扇豆器官脱落的首次基于转录组的全面表征,不仅为理解黄花羽扇豆的脱落信号通路提供了有价值的数据源,也为旨在提高作物产量的进一步研究提供了有价值的数据来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/efd433e8f4e6/fpls-08-00641-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/7cb27d48dfef/fpls-08-00641-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/efd433e8f4e6/fpls-08-00641-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/7cb27d48dfef/fpls-08-00641-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/d85c8edccbe2/fpls-08-00641-g0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/34bf470dbda6/fpls-08-00641-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/322cb17f1b5f/fpls-08-00641-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/d53f79ed66ed/fpls-08-00641-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/957992c6f92e/fpls-08-00641-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/c5d0f471ff6e/fpls-08-00641-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3599/5412092/efd433e8f4e6/fpls-08-00641-g0009.jpg

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