The Functional Significance of Mc MafF_G_K in Molluscs: Implications for Nrf2-Mediated Oxidative Stress Response

• Published in: International journal of molecular sciences 2023-11, Vol.24 (23)
• Main Authors: Yao, Ronghui, Qiu, Longmei, Zhu, Li, Chen, Xinglu, Zhai, Jiaying, Wang, Weifeng, Qi, Pengzhi, Liao, Zhi, Buttino, Isabella, Yan, Xiaojun, Guo, Baoying
• Format: Article
• Language: English
• ISSN: 1422-0067

The nuclear factor erythroid 2-related factor 2 (Nrf2) is a pivotal regulator of antioxidant gene expression in mammals, forming heterodimer complexes with small Maf proteins through its BZip domain. However, the underlying mechanism of Nrf2 action in molluscs remains poorly understood. The thick shell mussel, , represents a model organism for the marine environment and molluscs interaction research. In this study, we used in silico cloning to obtain a small Maf homologue called from . MafF_G_K possesses a typical BZip domain, suggesting its affiliation with the traditional small Maf family and its potential involvement in the Nrf2 signaling pathway. Transcriptional analysis revealed that MafF_G_K exhibited a robust response to benzo[a]pyrene (Bap) in the digestive glands. However, this response was down-regulated upon interference with MafF_G_K-siRNA. Interestingly, the expression levels of Nrf2, NAD(P)H: quinone oxidoreductase (NQO-1), and Glutathione Peroxidase (GPx), which are key players in oxidative stress response, showed a positive correlation with MafF_G_K in digested adenocytes of . Furthermore, in vitro analysis of antioxidant capacity in digestive gland cells demonstrated that Bap exposure led to an increase in reactive oxygen species (ROS) levels, accompanied by an elevation in total antioxidant capacity (T-AOC), potentially counterbalancing the excessive ROS. Strikingly, transfection of MafF_G_K siRNA resulted in a significant rise in ROS level and a down-regulation of T-AOC level. To validate the functional relevance of MafF_G_K, a glutathione S-transferase (GST) pull-down assay confirmed its interaction with Nrf2, providing compelling evidence of their protein interaction. This study significantly contributes to our understanding of the functional role of MafF_G_K in the Nrf2 signaling pathway and sheds light on its potential as a target for further research in oxidative stress response.