Lykov Nikita, Wang Huiling, Panga Mogellah John, Du Zhanxiang, Chen Ziyi, Chen Shitian, Zhu Lin, Zhao Ye
School of Pharmaceutical Sciences, Nanjing Tech University, Nanjing 211816, China.
School of Pharmaceutical Sciences, Nanjing Tech University, Nanjing 211816, China.
Tissue Cell. 2024 Dec;91:102600. doi: 10.1016/j.tice.2024.102600. Epub 2024 Oct 29.
The Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) play complex roles in liver health, influencing processes such as fibrosis, cancer development, and regeneration. WW domain binding protein-2 (WBP2) primarily enhances the co-translational activity of YAP/TAZ, which is crucial for the progression of liver diseases. Despite existing knowledge, the specific functions of WBP2 and its interactions with YAP remain inadequately understood. This study investigates the expression levels of WBP2 in zebrafish embryos and its molecular interaction with YAP. We employed morpholino-mediated knockdown of wbp2 and yap, followed by assessments of liver histology, immunofluorescence, and co-immunoprecipitation. Subsequently, RNA sequencing analyses were conducted to elucidate the signaling pathways and mechanisms underlying the interplay between YAP and WBP2 in liver injury. Our findings highlight the significant interaction between WBP2 and YAP, emphasizing their potential as therapeutic targets for liver diseases.
Yes相关蛋白(YAP)和具有PDZ结合基序的转录共激活因子(TAZ)在肝脏健康中发挥着复杂作用,影响着纤维化、癌症发展和再生等过程。WW结构域结合蛋白2(WBP2)主要增强YAP/TAZ的共翻译活性,这对肝脏疾病的进展至关重要。尽管已有相关认识,但WBP2的具体功能及其与YAP的相互作用仍未得到充分了解。本研究调查了斑马鱼胚胎中WBP2的表达水平及其与YAP的分子相互作用。我们采用吗啉代介导的wbp2和yap敲低,随后评估肝脏组织学、免疫荧光和免疫共沉淀。随后进行RNA测序分析,以阐明YAP和WBP2在肝损伤中相互作用的信号通路和机制。我们的研究结果突出了WBP2和YAP之间的显著相互作用,强调了它们作为肝脏疾病治疗靶点的潜力。