Your browser doesn't support javascript.
loading
Identification and expression profile analysis of the SnRK2 gene family in cucumber.
Wan, Zilong; Luo, Shilei; Zhang, Zeyu; Liu, Zeci; Qiao, Yali; Gao, Xueqin; Yu, Jihua; Zhang, Guobin.
Affiliation
  • Wan Z; Gansu Agricultural University, State Key Laboratory of Arid Land Crop Science, Lanzhou, China.
  • Luo S; College of Horticulture, Gansu Agricultural University, Lanzhou, China.
  • Zhang Z; Gansu Agricultural University, State Key Laboratory of Arid Land Crop Science, Lanzhou, China.
  • Liu Z; College of Horticulture, Gansu Agricultural University, Lanzhou, China.
  • Qiao Y; Gansu Agricultural University, State Key Laboratory of Arid Land Crop Science, Lanzhou, China.
  • Gao X; College of Horticulture, Gansu Agricultural University, Lanzhou, China.
  • Yu J; Gansu Agricultural University, State Key Laboratory of Arid Land Crop Science, Lanzhou, China.
  • Zhang G; College of Horticulture, Gansu Agricultural University, Lanzhou, China.
PeerJ ; 10: e13994, 2022.
Article in En | MEDLINE | ID: mdl-36164601
The sucrose non-fermenting-1-related protein kinase 2 (SnRK2) is a plant-specific type of serine/threonine protein kinase that plays an important role in the physiological regulation of stress. The objective of this study was to identify and analyze the members of the SnRK2 gene family in cucumber and lay a foundation for further exploration of the mechanism of CsSnRK2 resistance to stress. Here, 12 SnRK2 genes were isolated from cucumber and distributed on five chromosomes, phylogenetic clustering divided these into three well-supported clades. In addition, collinearity analysis showed that the CsSnRK2 gene family underwent purifying selection pressure during evolution. CsSnRK2 genes of the same group have similar exons and conserved motifs, and intron length may be a specific imprint for the evolutionary amplification of the CsSnRK2 gene family. By predicting cis elements in the promoter, we found that the promoter region of CsSnRK2 gene members had various cis-regulatory elements in response to hormones and stress. Relative expression analysis showed that CsSnRK2.11 (group II) and CsSnRK2.12 (group III) were strongly induced by ABA, NaCl and PEG stress; whereas CsSnRK2.2 (group III) was not activated by any treatment. The response of group I CsSnRK2 to ABA, NaCl and PEG was weak. Furthermore, protein interaction prediction showed that multiple CsSnRK2 proteins interacted with four proteins including protein phosphatase 2C (PP2C), and it is speculated that the CsSnRK2 genes may also an independent role as a third messenger in the ABA signaling pathway. This study provides a reference for analyzing the potential function of CsSnRK2 genes in the future research.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cucumis sativus Type of study: Diagnostic_studies Language: En Journal: PeerJ Year: 2022 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cucumis sativus Type of study: Diagnostic_studies Language: En Journal: PeerJ Year: 2022 Type: Article Affiliation country: China