RNA-seq analysis of watermelon (Citrullus lanatus) to identify genes involved in fruit cracking

被引:26
作者
Jiang, Haikun [1 ,2 ]
Tian, Hongmei [2 ]
Yan, Congsheng [2 ]
Jia, Li [2 ]
Wang, Yan [2 ]
Wang, Mingxia [2 ]
Jiang, Chang Jun [1 ]
Li, Yeyun [1 ]
Jiang, Jiayue [1 ]
Fang, Ling [2 ]
Zhang, Qi'an [2 ]
机构
[1] Anhui Agr Univ, Coll Tea & Food Technol, State Key Lab Tea Plant Biol & Utilizat, Hefei 230036, Anhui, Peoples R China
[2] Anhui Acad Agr Sci, Inst Hort, Key Lab Genet Improvement & Ecophysiol Hort Crop, Hefei 230031, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Citrullus lanatus; Watermelon; RNA-sequencing; Fruit cracking; Differentially expressed genes; Expression analysis; ARABIDOPSIS;
D O I
10.1016/j.scienta.2019.01.005
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
Fruit cracking in watermelon (Citrullus lanatus) causes a great economic loss. To understand the molecular mechanisms underlying watermelon fruit cracking, the differentially expressed genes (DEGs) between resistant and susceptible-cracking watermelon were analyzed using transcriptome sequencing. We selected the parent inbred W11 (resistant-cracking) and W13 (susceptible-cracking), and Near-Isogenic Lines W96 (resistant cracking) and W85 (susceptible-cracking) as materials. Differentially expressed genes (DEGs) analysis showed that 290 DEGs had detectable in "W11" VS "W13", while 165 DEGs had detectable in "W96" VS "W85". There were 56 DEGs between the four samples. Additionally, 14 DEGs related to fruit cracking were identified from the transcriptome. Only 8 DEGs among them, were involved in 14 KEGG pathway. The expression patterns of the 14 DEGs related to fruit cracking were analyzed by qRT-PCR to explore their putative functions. This transcriptome dataset will aid in understanding and carrying out future studies on the molecular basis of fruit cracking and contribute to watermelon breeding..
引用
收藏
页码:248 / 255
页数:8
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