Transcriptomic analysis reveals insights into the response to Hop stunt viroid (HSVd) in sweet cherry (Prunus avium L.) fruits

被引:8
作者
Xu, Li [1 ]
Zong, Xiaojuan [1 ]
Wang, Jiawei [1 ]
Wei, Hairong [1 ]
Chen, Xin [1 ]
Liu, Qingzhong [1 ]
机构
[1] Shandong Inst Pomol, Key Lab Fruit Biotechnol Breeding Shandong Prov, Tai An, Shandong, Peoples R China
关键词
Sweet cherry; Hop stunt viroid; Transcriptome; RT-qPCR; SPINDLE TUBER VIRUS; GENE-EXPRESSION; PLANT-VIRUS; ARABIDOPSIS; DISEASE; FAMILY; BIOSYNTHESIS; RESISTANCE; DEFENSE; CITRUS;
D O I
10.7717/peerj.10005
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hop stunt viroid (HSVd) is a member of the genus Hostuviroid of the family Pospiviroidae and has been found in a wide range of herbaceous and woody hosts. It causes serious dapple fruit symptoms on infected sweet cherry, notably inducing cherry tree decay. In order to better understand the molecular mechanisms of HSVd infection in sweet cherry fruit, transcriptome analysis of HSVd-infected and healthy sweet cherry fruits was carried out. A total of 1,572 differentially expressed genes (DEGs) were identified, involving 961 upregulated DEGs and 611 downregulated DEGs. Functional analysis indicated that the DEGs were mainly involved in plant hormone signal transduction, plant-pathogen interactions, secondary metabolism, and the MAPK signaling pathway. In addition, C2H2 zinc finger, MYB, bHLH, AP2/ERF, C2C2-dof, NAC and WRKY transcription factors can respond to HSVd infection. In order to confirm the high-throughput sequencing results, 16 DEGs were verified by RT-qPCR analysis. The results provided insight into the pathways and genes of sweet cherry fruit in response to HSVd infection.
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页数:22
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