文章摘要
Comparative Transcriptome Analysis of DcCIPK24 Transgenic Arabidopsis Under Salt Stress
  
DOI:10.16768/j.issn.1004-874X.2023.10.009
Author NameAffiliation
ZHANG Tingting1, TAN Yongqiang1, LIU Ying1, YUAN Gaigai1, RUI Rongtao1, ZHOU Yang2, LING Dong1 1. 襄阳市农业科学院湖北 襄阳 4410572. 海南大学热带农林学院(农业农村学院、乡村振兴学院)/海南省热带园艺作物品质调控重点实验室海南 海口 570228 
Hits: 617
Download times: 668
Abstract:
      【Objective】This study aimed to explore the downstream response genes of Dendrobium catenatum Lindl. DcCIPK24, and provided guidance for studying the molecular regulatory pathway of DcCIPK24 to improve salt tolerance. 【Method】The DcCIPK24 transgenic Arabidopsis thaliana and wild type plants under 200 mmol/L NaCl treatment and normal conditions were used for RNA-seq on the illumina NovaSeq 6000 sequencing platform. The enrichment pathway of differentially expressed genes (DEGs) was analyzed, and their expression patterns were verified by quantitative real-time PCR. 【Result】A total of 96 DEGs were identified from transgenic A. thaliana and wild type plants under salt stress. GO annotation analysis showed that 96 DEGs were mainly enriched in molecular function pathways. KEGG enrichment analysis found that DEGs enriched in amino sugar and nucleotide sugar metabolism, plant MAPK signaling pathway and glycerolipid metabolism. The DEGs including four upregulated genes (AtGPAT5, AtSIRK, AtMEE25, and AtUGE5) and four downregulated genes (AtAMT1-2, AtATTI3, AtCYP71A25, and AtLHCB4.3) were selected for qRT-PCR validation. The results showed that the trends of 8 DEGs’ expression were basically consistent with the RNA-seq data. 【Conclusion】DcCIPK24 responded to salt tolerance mainly through amino sugar and nucleotide sugar metabolism, plant MAPK signaling pathway, and glycerolipid metabolism.
View Full Text   View/Add Comment  Download reader