华北农学报 ›› 2020, Vol. 35 ›› Issue (1): 8-21. doi: 10.7668/hbnxb.20190649

所属专题: 玉米 热点文章

• 作物遗传育种·种质资源·生物技术 • 上一篇    下一篇

转录组及代谢组联合解析玉米响应花粒期高温胁迫机制

李川, 乔江方, 黄璐, 张美微, 张盼盼, 牛军, 刘京宝   

  1. 河南省农业科学院 粮食作物研究所, 河南 郑州 450002
  • 收稿日期:2019-10-27 出版日期:2020-02-28
  • 通讯作者: 刘京宝(1965-),男,河南鹿邑人,研究员,硕士,主要从事玉米高产抗逆栽培研究。
  • 作者简介:李川(1985-),女,河南新乡人,助理研究员,博士,主要从事玉米栽培生理生化研究。
  • 基金资助:
    “十三五”重点研究计划课题(2017YFD0300407;2017YFD0301102;2016YFD0100103);国家自然科学基金项目(31701368)

Transcriptome and Metabolome Analysis to Reveal the Mechanisms Responding to High Temperature Stress in Anthesis Stage of Maize

LI Chuan, QIAO Jiangfang, HUANG Lu, ZHANG Meiwei, ZHANG Panpan, NIU Jun, LIU Jingbao   

  1. Cereal Crops Institute, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China
  • Received:2019-10-27 Published:2020-02-28

摘要: 为了探明我国玉米主要推广品种郑单958、先玉335花粒期高温胁迫下基因表达及代谢物差异,挖掘玉米响应高温胁迫的关键基因及代谢物,利用Illumina HiSeqTM 2500高通量测序技术分别对郑单958、先玉335高温胁迫7,14 d的穗位叶及对照叶进行高通量转录组测序,利用广泛靶向代谢组测序技术对样品进行高通量代谢物测序。转录组测序共获得214.81 Gb干净序列。郑单958高温胁迫7 d后检测到49个差异表达基因,其中24个为上调基因。继续高温胁迫14 d共检测到306个差异表达基因,其中130个为上调基因。高温胁迫7 d与高温胁迫14 d对比组中检测到1 462个差异表达基因,其中647个为上调基因。先玉335高温胁迫7 d后共检测到381个差异表达基因,164个上调基因。继续高温胁迫14 d后共检测到299个差异表达基因,226个为上调基因。高温胁迫7 d与高温胁迫14 d对比组中共检测到2 481个差异表达基因,其中1 275个上调基因。在郑单958、先玉335高温胁迫7 d后对比组中检测到6 646个差异表达基因,其中3 253个上调基因。在郑单958、先玉335高温胁迫14 d对比组中检测到5 958个差异表达基因,其中3 110个上调基因。代谢物测序共检测到654个代谢物,郑单958高温胁迫7 d后共检测出28个差异代谢物,共注释到5个代谢通路中。高温胁迫14 d后共检测出54个差异代谢物,共注释到13个代谢通路中,其中9个差异代谢物呈上调表达。先玉335高温胁迫7 d后检测出98个差异代谢物,共注释到24个代谢通路中,其中43个差异代谢物呈上调表达。先玉335高温胁迫14 d后共检测出38个差异代谢物,共注释到13个代谢通路中,其中14个上调表达。郑单958高温胁迫7 d与先玉335高温胁迫7 d对比组共检测出144个差异代谢物,共注释到36个代谢通路中,其中81个差异代谢物呈上调表达。郑单958高温胁迫14 d与先玉335高温胁迫14 d对比组共检测出158个差异代谢物,共注释到40个代谢通路中,其中81个差异代谢物呈上调表达。

关键词: 玉米, 高温胁迫, 花粒期, 高通量转录组测序, 代谢组学分析, 差异表达基因

Abstract: The aim of the study was to explore differential expression of genes and metabolites in Zhengdan 958 and Xianyu 335 exposed to high temperature for 7,14 d during grain filling stage and identify the key candidate genes,transcription factors and metabolites,so as to understand molecular mechanism of high temperature tolerance in maize. The ear-leaf samples collected before high temperature treated(CK),7 d high temperature treated,14 d from Zhengdan 958 and Xianyu 335 were used for RNA-sequencing using Illumina HiSeqTM 2500 high-throughput sequencing technology. Metabolome variations analyzed using liquid-chromatography-mass spectrometry-based metabolomics. A total of 214.81 Gb clean sequence was obtained by transcriptome sequencing. In Zhengdan 958,49 DEGs were detected after 7 days of high temperature treated,of which 24 were up-regulated genes. 306 DEGs were detected after 14 d,130 of which were up-regulated genes. 1 462 DEGs were detected from 7 d samples compared with 14 d samples,of which 647 were up-regulated genes. In Xianyu 335,381 DEGs were detected after 7 days of high temperature treated,of which 164 were up-regulated genes. 299 DEGs were detected after 14 d,226 of which were up-regulated genes. 2 481 DEGs were detected from 7 d treated samples compared with 14 d treated samples,of which 1 275 were up-regulated genes. Comparing Zhengdan 958 samples treated for 7 d with Xianyu 335 samples treated for 7 d,6 646 DEGs were detected,of which 3 253 up-regulated genes. Comparing Zhengdan 958 samples treated for 14 d with Xianyu 335 samples treated for 14 d,5 958 DEGs were detected,of which 3 110 up-regulated genes. A total of 654 metabolites were detected by metabolomics sequencing. In Zhengdan 958,28 DEMs were detected after 7 days of high temperature treated and were annotated into 5 metabolic pathways. 54 DEMs were detected after 14 days,9 of which were up-regulated,and were annotated into 13 metabolic pathways. In Xianyu 335, 98 DEMs were detected after 7 d of high temperature treated,43 of which were up-regulated and were annotated into 24 metabolic pathways. 38 DEMs were detected after 14 d,14 of which were up-regulated,and were annotated into 13 metabolic pathways. Compared Zhengdan 958 with Xianyu 335,144 DEMs were detected after 7 days,81 of which were up-regulated,and were annotated into 36 metabolic pathways.158 DEMs were detected after 14 days,81 of which were up-regulated,and were annotated into 40 metabolic pathways.

Key words: Maize, High temperature stress, Anthesis stage, Illumina RNA-sequencing, Metabolomics profiling, Differentially expressed gene(DEG)

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引用本文

李川, 乔江方, 黄璐, 张美微, 张盼盼, 牛军, 刘京宝. 转录组及代谢组联合解析玉米响应花粒期高温胁迫机制[J]. 华北农学报, 2020, 35(1): 8-21. doi: 10.7668/hbnxb.20190649.

LI Chuan, QIAO Jiangfang, HUANG Lu, ZHANG Meiwei, ZHANG Panpan, NIU Jun, LIU Jingbao. Transcriptome and Metabolome Analysis to Reveal the Mechanisms Responding to High Temperature Stress in Anthesis Stage of Maize[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2020, 35(1): 8-21. doi: 10.7668/hbnxb.20190649.

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