N6-methyladenosine modification of PLOD2 causes spermatocyte damage in rats with varicocele

作者：Huan Li, Jun Zhao, Hao Deng, Yucheng Zhong, Mian Chen, LinSheng Chi, Guoqun Luo, Cong Cao, Cong Yu, Honghai Liu, Xinzong Zhang · 发表于：Cellular & Molecular Biology Letters · 年份：2023 · DOI：10.1186/s11658-023-00475-4 · 被引用次数：15 · 研究领域：RNA modifications and cancer、Cancer-related molecular mechanisms research、Cancer-related gene regulation

Abstract Background In recent years, N6-methyladenosine (m 6 A) methylation modification of mRNA has been studied extensively. It has been reported that m 6 A determines mRNA fate and participates in many cellular functions and reactions, including oxidative stress. The PLOD2 gene encodes a protein that plays a key role in tissue remodeling and fibrotic processes. Methods The m 6 A methylation and expression levels of PLOD2 were determined by m 6 A methylated RNA immunoprecipitation sequencing (MeRIP-seq) and MeRIP-quantitative polymerase chain reaction (qPCR) in the testes of varicocele rats compared with control. To determine whether IGF2BP2 had a targeted effect on the PLOD2 mRNA, RNA immunoprecipitation-qPCR (RIP-qPCR) and luciferase assays were performed. CRISPR/dCas13b-ALKBH5 could downregulate m 6 A methylation level of PLOD2 , which plays an important role in PLOD2 -mediated cell proliferation and apoptosis in GC-2 cells. Results PLOD2 was frequently exhibited with high m 6 A methylation and expression level in the testes of varicocele rats compared with control. In addition, we found that IGF2BP2 binds to the m 6 A-modified 3′ untranslated region (3′-UTR) of PLOD2 mRNA, thereby positively regulating its mRNA stability. Targeted specific demethylation of PLOD2 m 6 A by CRISPR/dCas13b-ALKBH5 system can significantly decrease the m 6 A and expression level of PLOD2 . Furthermore, demethylation of PLOD2 mRNA dramatically promote GC-2 cell proliferation and inhibit cell a...