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首页> 外文期刊>Tropical plant biology >RNA-Seq De Novo Assembly of Red Pitaya (Hylocereus polyrhizus) Roots and Differential Transcriptome Analysis in Response to Salt Stress
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RNA-Seq De Novo Assembly of Red Pitaya (Hylocereus polyrhizus) Roots and Differential Transcriptome Analysis in Response to Salt Stress

机译:RNA-SEQ de Novo组装红斗牛(Hylocereus polyrhizus)根系和差异转录组分析响应盐胁迫

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摘要

Pitaya (Hylocereus polyrhizus) is a highly valued functional food that is widely planted in Southeast Asia. However, with increased soil salinization in cultivation areas, a better understanding of the molecular mechanisms associated with salt stress responses in red pitaya is necessary. Herein, RNA-Seq was used to de novo assemble and characterize the transcriptomic profiles of red pitaya roots in response to salt stress. A total of 73,589 transcripts were obtained and the average sequence length was 1308bp. From these transcripts, 26,878 unique transcripts were successfully matched to 13,519 Swiss-prot proteins. Gene ontology (GO) annotations showed that within the categories of molecular function, biological function, and cell component, catalytic activity (GO:0003824), metabolic process (GO:0008152), and cell part (GO:0044464) were the most enriched, respectively. 2624 transcripts were significantly differentially expressed among three time points (3h, 7h, and 30h) following exposure to 450mM NaCl. Furthermore, 261 genes were up-regulated and 61 down-regulated in all three of the time points. Glycolysis/gluconeogenesis was one of the most significantly modulated pathways. The findings presented herein provide further insight into salt stress responses in pitaya and will provide a valuable resource for future functional studies examining salt adaptations.
机译:Pitaya(Hylocereus polyrhizus)是一种高度重视的功能性食品,广泛种植在东南亚。然而,随着培养区域的土壤盐渍化增加,需要更好地了解与盐胁迫反应在红色筏中的分子机制是必要的。这里,RNA-SEQ用于De Novo组装并表征响应于盐胁迫的红色斗叶根的转录组谱。获得了总共73,589种转录物,平均序列长度为1308bp。从这些转录物中,26,878个独特的转录物成功匹配至13,519瑞士蛋白质。基因本体(GO)注释显示,在分子功能,生物学功能和细胞成分的类别内,催化活性(GO:0003824),代谢过程(GO:0008152)和细胞部分(GO:0044464)是最丰富的, 分别。在暴露于450mm NaCl后,在350mm的三个时间点(3h,7h和30h)中,2624转录物显着表达。此外,261个基因上调,并且在所有三个时间点中下调61个。糖酵解/葡糖生成是最显着的调制途径之一。本文所提出的发现进一步了解脱皮中的盐应激反应,并将为未来的功能研究提供有价值的资源,用于检查盐适应。

著录项

  • 来源
    《Tropical plant biology》 |2019年第2期|共12页
  • 作者单位

    Chinese Acad Sci South China Bot Garden Key Lab South China Agr Plant Mol Anal &

    Genet Im 723 Xingkelu Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Key Lab South China Agr Plant Mol Anal &

    Genet Im 723 Xingkelu Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Key Lab South China Agr Plant Mol Anal &

    Genet Im 723 Xingkelu Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Key Lab South China Agr Plant Mol Anal &

    Genet Im 723 Xingkelu Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Key Lab South China Agr Plant Mol Anal &

    Genet Im 723 Xingkelu Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Guangdong Prov Key Lab Appl Bot Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Guangdong Prov Key Lab Appl Bot Guangzhou 510650 Guangdong Peoples R China;

    Chinese Acad Sci South China Bot Garden Key Lab South China Agr Plant Mol Anal &

    Genet Im 723 Xingkelu Guangzhou 510650 Guangdong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物学;
  • 关键词

    Pitaya; Salt stress; RNA-Seq; De novo; Transcriptome;

    机译:pitaya;盐胁迫;RNA-SEQ;再次;转录组;

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