RNA-seq analysis and transcriptome assembly of Salicornia neei reveals a powerful system for ammonium detoxification

IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Electronic Journal of Biotechnology Pub Date : 2022-07-01 DOI:10.1016/j.ejbt.2022.05.003
Mónica Díaz-Silva , Jonathan Maldonado , Pamela Veloso , Nicol Delgado , Herman Silva , José A. Gallardo
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Abstract

Background

Salicornia neei is a halophyte plant that has been proposed for use in the phytoremediation of the saline wastewater generated by land-based aquaculture. To identify the molecular mechanisms related to ammonium response, we analyzed the transcriptome of S. neei in response to growth in saline water containing 3 mM ammonium.

Results

The RNA sequencing generated a total of 14,680,108 paired-end reads from the control and stressed conditions. De novo assembly using the CLC Genomic Workbench produced 86,020 transcripts and a reference transcriptome with an N50 of 683 base pair.

A total of 45,327 genes were annotated, representing 51.2% of the contig predicted from de novo assembly. As regards differentially expressed genes, a total of 9,140 genes were differentially expressed in response to ammonium in saline water; of these, 7,396 could be annotated against functional databases. The upregulated genes were mainly involved in cell wall biosynthesis, transmembrane transport and antiporter activities, including biological Kyoto Encyclopedia of Genes and Genomes, pathways linked to the biosynthesis of secondary metabolites, plant hormone signal transduction, autophagy, and nitrogen metabolism. In addition, a set of 72 genes was directly involved in ammonium metabolism, including glutamine synthetase 1, glutamate synthase 1, and ferredoxin-dependent glutamate synthase chloroplastic.

Conclusions

Our results support the hypothesis that an ammonium detoxification system mediated by glutamine and glutamate synthase was activated in S. neei when exposed to ammonium and saline water. The present transcriptome profiling method could be useful when investigating the response of halophyte plants to saline wastewater from land-based aquaculture.

This manuscript includes an interactive 360 degree video, supplementary to the materials and methods section. To view the video correctly, it is necessary to scroll through the screen to navigate across the laboratory where you will find 6 interactive points. For an immersive experience a head-mounted display can be used. Please, visit this URL: http://ejbiotechnology.info/public/360view/2022/VTPGALLARDO_1v3/index.htm.

How to cite: Díaz-Silva M, Maldonado J, Veloso P, et al. RNA-seq analysis and transcriptome assembly of Salicornia neei reveals a powerful system for ammonium detoxification. Electron J Biotechnol 2022;58. https://doi.org/10.1016/j.ejbt.2022.05.003

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盐角草的RNA-seq分析和转录组组装揭示了一个强大的氨解毒系统
盐角草(salicornia nei)是一种盐生植物,已被提议用于陆地水产养殖产生的含盐废水的植物修复。为了确定与铵响应相关的分子机制,我们分析了麻豆在含3 mM铵的盐水中生长的转录组。结果在对照和应激条件下,RNA测序共产生14,680,108对末端reads。使用CLC基因组工作台重新组装产生86,020个转录本和一个N50为683碱基对的参考转录组。共有45327个基因被注释,占从头组装预测的基因组的51.2%。在差异表达基因方面,盐水铵处理下共有9140个差异表达基因;其中,7396个可以针对功能数据库进行注释。上调的基因主要参与细胞壁生物合成、跨膜转运和反转运活性,包括生物京都基因和基因组百科全书、次生代谢物生物合成相关途径、植物激素信号转导、自噬和氮代谢。此外,有72个基因直接参与氨代谢,包括谷氨酰胺合成酶1、谷氨酸合成酶1和铁氧化还蛋白依赖的谷氨酸合成酶叶绿体。结论研究结果支持了谷氨酰胺和谷氨酸合成酶介导的谷氨酸脱毒系统在铵盐和盐水环境下被激活的假说。该转录组分析方法可用于研究盐生植物对陆源水产养殖含盐废水的反应。这份手稿包括一个交互式360度视频,补充材料和方法部分。为了正确地观看视频,有必要滚动屏幕以在实验室中导航,在那里你会发现6个互动点。为了获得身临其境的体验,可以使用头戴式显示器。请访问这个网址:http://ejbiotechnology.info/public/360view/2022/VTPGALLARDO_1v3/index.htm.How引用:Díaz-Silva M, Maldonado J, Veloso P,等人。盐角草的RNA-seq分析和转录组组装揭示了一个强大的氨解毒系统。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2022.05.003
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Electronic Journal of Biotechnology
Electronic Journal of Biotechnology 工程技术-生物工程与应用微生物
CiteScore
5.60
自引率
0.00%
发文量
50
审稿时长
2 months
期刊介绍: Electronic Journal of Biotechnology is an international scientific electronic journal, which publishes papers from all areas related to Biotechnology. It covers from molecular biology and the chemistry of biological processes to aquatic and earth environmental aspects, computational applications, policy and ethical issues directly related to Biotechnology. The journal provides an effective way to publish research and review articles and short communications, video material, animation sequences and 3D are also accepted to support and enhance articles. The articles will be examined by a scientific committee and anonymous evaluators and published every two months in HTML and PDF formats (January 15th , March 15th, May 15th, July 15th, September 15th, November 15th). The following areas are covered in the Journal: • Animal Biotechnology • Biofilms • Bioinformatics • Biomedicine • Biopolicies of International Cooperation • Biosafety • Biotechnology Industry • Biotechnology of Human Disorders • Chemical Engineering • Environmental Biotechnology • Food Biotechnology • Marine Biotechnology • Microbial Biotechnology • Molecular Biology and Genetics •Nanobiotechnology • Omics • Plant Biotechnology • Process Biotechnology • Process Chemistry and Technology • Tissue Engineering
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