Xiongze Dai

Xiongze Dai


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2020 in Food Chemistry
Verified
Journal Article
Closed access
YLYuhua Liu
Yuhua Liu
JLJunheng Lv
Junheng Lv
ZLZhoubin Liu
Zhoubin Liu
JWJing Wang
Jing Wang
BYBozhi Yang
Bozhi Yang
ZXZou Xuexiao
Zou Xuexiao

21 August 2018 in New Phytologist
Verified
Journal Article
Open access
PDF file
LOLijun Ou
Lijun Ou
DLDong Li
Dong Li
JLJunheng Lv
Junheng Lv
WCWenchao Chen
Wenchao Chen
ZZZhuqing Zhang
Zhuqing Zhang
ZXZou Xuexiao
Zou Xuexiao

1 April 2019 in Ecotoxicology and Environmental Safety
Verified
Journal Article
Closed access
BMBaobin Mi
Baobin Mi
FLFeng Liu
Feng Liu
LXLingling Xie
Lingling Xie
HZHuoqiang Zhou
Huoqiang Zhou
FWfangfang wu
fangfang wu
XDXiongze Dai
Xiongze Dai


20 October 2010 in JOURNAL OF HUNAN AGRICULTURAL UNIVERSITY
Verified
Journal Article
Closed access
XZXi-Lu Zhang
Xi-Lu Zhang
FLFeng Liu
Feng Liu
XDXiongze Dai
Xiongze Dai
YMYanqing Ma
Yanqing Ma
ZYZu-Hua Yuan
Zu-Hua Yuan
HCHui-Ming Chen
Hui-Ming Chen
Based on the sequences of CsACS1G,CsACS1 and BCAT,the specific PCR primers were designed to identify CsACS1G gene using DNA markers in Cucumber (Cucumis sativus L.),and genome DNA was rapidly extracted from cucumber WI1983G,95,98-17,S2-98 and offspring 95×WI1983G with the method of NaOH.Field surveys were conducted in the flowering period so as to confirm stability of the primers.The results showed that DNA molecular marker can amplify a specific fragment of CsACS1G gene when the resultant DNA was used as PCR template.So,identification of CsACS1G gene DNA molecular markers and the method of DNA rapid extraction in cucumber would provide the conditions to accelerating breeding of gynoecium's cucumber.

4 May 2022 in Frontiers in Plant Science
Verified
Journal Article
Open access
BTBingqian Tang
Bingqian Tang
LXLingling Xie
Lingling Xie
HYHuiping Yang
Huiping Yang
XLXiumin Li
Xiumin Li
YCYing Chen
Ying Chen
XDXiongze Dai
Xiongze Dai
The mechanism of resistance of plants to cold temperatures is very complicated, and the molecular mechanism and related gene network in pepper are largely unknown. Here, during cold treatment, we used cluster analysis (k-means) to classify all expressed genes into 15 clusters, 3,680 and 2,405 differentially expressed genes (DEGs) were observed in the leaf and root, respectively. The DEGs associated with certain important basic metabolic processes, oxidoreductase activity, and overall membrane compositions were most significantly enriched. In addition, based on the homologous sequence alignment of Arabidopsis genes, we identified 14 positive and negative regulators of the ICE-CBF-COR module in pepper, including CBF and ICE, and compared their levels in different data sets. The correlation matrix constructed based on the expression patterns of whole pepper genes in leaves and roots after exposure to cold stress showed the correlation between 14 ICE-CBF-COR signaling module genes, and provided insight into the relationship between these genes in pepper. These findings not only provide valuable resources for research on cold tolerance, but also lay the foundation for the genetic modification of cold stress regulators, which would help us achieve improved crop tolerance. To our knowledge, this is the first study to demonstrate the relationship between positive and negative regulators related to the ICE-CBF-COR module, which is of great significance to the study of low-temperature adaptive mechanisms in plants.