数字农科院2.0

Alteration of gene expression profile in the roots of wild diploid Arachis duranensis inoculated with Ralstonia solanacearum

文献类型: 外文期刊

作者: Chen, Y. N.;Ren, X. P.;Zhou, X. J.;Huang, L.;Huang, J. Q.;Yan, L. Y.;Lei, Y.;Wei, W. H.;Jiang, H. F.;Qi, Y.

作者机构:

关键词: Arachis duranensis;DEGs;Ralstonia solanacearum;real-time PCR;SSH

期刊名称: PLANT PATHOLOGY

ISSN:

年卷期:

页码:

收录情况: SCI

摘要: Bacterial wilt caused by Ralstonia solanacearum is a serious disease of peanut (Arachis hypogaea) in China. However, the molecular basis of peanut resistance to R. solanacearum is poorly understood. Arachis duranensis, a wild diploid species of the genus Arachis, has been proven to be resistant to bacterial wilt, and thus holds valuable potential for understanding the mechanism of resistance to bacterial wilt and genetic improvement of peanut disease resistance. Here, suppression subtractive hybridization (SSH) and macroarray hybridization were employed to detect differentially expressed genes (DEGs) in the roots of A. duranensis after R. solanacearum inoculation. A total of 317 unique genes were obtained, 265 of which had homologues and functional annotations. KEGG analysis revealed that a large proportion of these unigenes are mainly involved in the biosynthesis of phytoalexins, particularly in the biosynthetic pathways of terpenoids and flavonoids. Subsequent real-time polymerase chain reaction (PCR) analysis showed that the terpenoid and flavonoid synthesis-related genes showed higher expression levels in a resistant genotype of A. duranensis than in a susceptible genotype, indicating that the terpenoids and flavonoids probably played a fundamental role in the resistance of A. duranensis to R. solanacearum. This study provides an overview of the gene expression profile in the roots of wild Arachis species in response to R. solanacearum infection. Moreover, the related candidate genes are also valuable for the further study of the molecular mechanisms of resistance to R. solanacearum.

分类号: S432.1

  • 相关文献

[1]Dynamics in the resistant and susceptible peanut (Arachis hypogaea L.) root transcriptome on infection with the Ralstonia solanacearum. Chen, Yuning,Ren, Xiaoping,Zhou, Xiaojing,Huang, Li,Yan, Liying,Lei, Yong,Liao, Boshou,Huang, Shunmou,Wei, Wenhui,Jiang, Huifang,Huang, Jinyong. 2014

[2]The regulation of BbLaeA on the production of beauvericin and bassiatin in Beauveria bassiana. Yin M., Xiao D., Wang C., Zhang L., Dun B., Yue Q.. 2022

[3]利用RNAi研究棉花SSH文库上调表达EST的功能. 尹国,路正营,李世云,韩永亮,张朝军,李付广. 2018

[4]植物差异表达基因克隆技术及研究进展. 谢伟伟,王凭青,杨青川,刘博,李志中. 2005

[5]黄萎病菌诱导下的陆地棉高抗黄萎病品种SSH文库的初步构建. 王升正,齐放军,简桂良. 2009

[6]干旱胁迫下棉花SSH文库构建及其抗旱相关基因分析. 王德龙,叶武威,王俊娟,宋丽艳,樊伟丽,崔宇鹏. 2010

[7]短枝型苹果SSH文库构建及相关基因表达分析. 宋杨,吴树敬,张艳敏,陈学森. 2013

[8]抑制差减杂交(SSH)技术及其在植物基因分离上的应用. 李广存,金黎平,谢开云,屈冬玉. 2004

[9]激活蛋白处理水稻引发基因差异表达的研究. 杨勇,谢馥交,刘峥,邱德文,杨秀芬. 2006

[10]几种基因差异表达筛选技术在动物发育与繁殖中的最新进展. 肖朝庭,储明星,傅衍. 2006

[11]Comparative transcript profiling of gene expression of fresh and frozen-thawed bull sperm. Chen, Xiaoli,Zhu, Huabin,Hao, Haisheng,Zhao, Xueming,Qin, Tong,Wang, Dong,Wang, Yonggui.

[12]Construction and application of EST library from Setaria italica in response to dehydration stress. Zhang, Jinpeng,Liu, Tingsong,Fu, Junjie,Zhu, Yun,Jia, Jinping,Zheng, Jun,Zhao, Yinhe,Zhang, Ying,Wang, Guoying.

[13]Identification of the genes and pathways associated with pigment gland morphogenesis in cotton by transcriptome profiling of near-isogenic lines. Quan Sun,Shengwei Li,Min Chen,Yingfan Cai,Jianchuan Mo,Xiaohong He,Huaizhong Jiang,JinggaoLiu,Kairong Lei.

[14]Latest Advances in Watermelon Genomics. Guo, Shaogui,Xu, Yong,Zhang, Haiying,Gong, Guoyi,Guo, Shaogui,Zheng, Yi,Fei, Zhangjun,Huang, Sanwen,Yi, Hongping,Wu, Mingzhu,Fei, Zhangjun,Zheng, Yi. 2010

[15]铜胁迫对农田土壤酶活性、细菌和古菌数量的影响. 王斐,黄益宗,王小玲,高柱,余发新,徐峰,保琼莉,胡莹,乔敏. 2014

[16]水稻根系不同强度干旱胁迫下5个基因表达分析. 马廷臣,陈荣军,余蓉蓉,曾汉来,张端品. 2010

[17]非洲猪瘟病毒常规PCR及Real-time PCR检测方法的建立. 张泉,朱鸿飞,孙怀昌. 2007

[18]不同剂量胰岛素、胰高血糖素和甲状腺素处理对奶牛乳腺上皮细胞FcRn mRNA表达的影响. 胡小丽,张春林,王加启,赵圣国,章玉涛,卜登攀,周凌云. 2011

[19]大豆C3HC4型RING锌指蛋白基因GmRZFP1克隆与表达分析. 吴学闯,曹新有,陈明,张晓科,刘阳娜,徐兆师,李连城,马有志. 2010

[20]陆地棉质体转录活性因子基因GhPTAC的克隆及其耐盐性分析. 叶武威,王俊娟,王德龙,樊保香,王帅. 2011

作者其他论文 更多>>