Author:
Xiao Zhijing,Lu Yanke,Zou Yi,Zhang Chi,Ding Li,Luo Kai,Tang Qiaoyu,Zhou Yifeng
Abstract
Abstract
Background
ATP sulfurylase (ATPS) is a crucial enzyme for the selenate assimilation pathway in plants.
Results
In this study, genome-wide and comparative analyses of ATPS in Cardamine hupingshanensis, including sequence and structural analyses, were performed. The expression of ChATPS gene family members in C. hupingshanensis under selenium (Se) stress was also investigated, and our results suggest that ChATPS1-2 play key roles in the response to Se stress. Nine ATPS genes were found from C. hupingshanensis, which share highly conserved sequences with ATPS from Arabidopsis thaliana. In addition, we performed molecular docking of ATP sulfurylase in complex with compounds ATP, selenate, selenite, sulfate, and sulfite. ChAPS3-1 was found to have stronger binding energies with all compounds tested. Among these complexes, amino acid residues Arg, Gly, Ser, Glu, and Asn were commonly present.
Conclusion
Our study reveals the molecular mechanism of C. hupingshanensis ATP sulfurylase interacting with selenate, which is essential for understanding selenium assimilation. This information will guide further studies on the function of the ChATPS gene family in the selenium stress response and lay the foundation for the selenium metabolic pathway in higher plants.
Funder
the National Natural Science Foundation of China
the Enshi Autonomous Prefecture Science and Technology Program
the Excellent Young and Middle-aged Scientific and Technological Innovation Team Projects of Colleges and Universities in Hubei Province
the Open Foundation of Hubei Key Laboratory of Biological Resources Protection and Utilization
Publisher
Springer Science and Business Media LLC