Genome-Wide Identification and Expression Analysis of Tomato ADK Gene Family during Development and Stress

被引:13
作者
Yang, Lu [1 ]
Cao, Haohao [2 ]
Zhang, Xiaoping [1 ]
Gui, Liangxian [1 ]
Chen, Qiang [1 ]
Qian, Gui [1 ]
Xiao, Jiaxin [1 ]
Li, Zhengguo [2 ]
机构
[1] Anhui Normal Univ, Coll Life Sci, Key Lab Conservat & Utilizat Important Biol Resou, Wuhu 241000, Peoples R China
[2] Chongqing Univ, Sch Life Sci, Key Lab Plant Hormones & Dev Regulat Chongqing, Chongqing 400044, Peoples R China
关键词
genome-wide; tomato; ADK gene family; stress; ADENINE-NUCLEOTIDE RATIOS; ADENYLATE KINASE; ENERGY-CHARGE; SIGNAL-TRANSDUCTION; DROUGHT STRESS; ABSCISIC-ACID; MITOCHONDRIA; RESPONSES; PROTEIN; SALT;
D O I
10.3390/ijms22147708
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenylate kinase (ADK) is widely distributed in organisms and plays an important role in cellular energy homeostasis. In plants, ADK has important functions in plant growth and development regulation as well as in adaptation to the environment. However, little information is available about the ADK genes in tomato (Solanum lycopersicum), an important economic crop. To investigate the characteristics and functions of ADK genes in tomato, a total of 11 ADK genes were identified and named according to their chromosomal locations. The ADK family in Arabidopsis, tomato, potato, and rice was divided into six groups, and motif analysis revealed that each SlADK protein contained five to eight conserved motifs. A total of 4 to 19 exons were identified in tomato ADK gene family members, and interestingly, most members possessed 4 exons. Several stress response elements were identified in the promoter regions of SlADKs. The 11 SlADKs were randomly distributed on 9 of the 12 tomato chromosomes. Three duplication events were observed between tomato chromosomes, and a high degree of conservation of synteny was demonstrated between tomato and potato. The online TomExpress platform prediction revealed that SlADKs were expressed in various tissues and organs, basically consistent with the data obtained from real-time quantitative PCR (qPCR). The qPCR verification was also performed to determine the expression level of SlADKs and demonstrated that the genes responded to multiple abiotic stresses, such as drought, salt, and cold. Besides, the qPCR results showed that SlADK transcription was responsive to most of the applied hormone treatment. For correlation network analysis under 44 global conditions, the results showed that the number of 17, 3, 4, and 6 coexpressed genes matched with SlADK5, 8, 9, and 11, respectively. For specific gene function analysis, expression of SlADK10 was inhibited using virus-induced gene silencing (VIGS). Compared to wild-type plants, plants with silenced SlADK10 gene had poor drought resistance, indicating SlADK10 regulated drought tolerance of tomato positively. In summary, the information provided in the present study will be helpful to understand the evolutionary relationship and their roles of tomato ADK gene family in further research.
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页数:23
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