The RNA m5C methylase NSUN4 protects retinal ganglion cells by regulating m5C methylation in the Hedgehog signaling pathway

Author:

Li Yahong1,Li Dian2,Geng Chao3,Wei Ruihua4,Duan Yajian1

Affiliation:

1. Shanxi Bethune Hospital

2. Washington University School of Medicine in St. Louis

3. Nankai University

4. Tianjin Medical University Eye Hospital

Abstract

Abstract

Glaucoma, one of the leading causes of blindness worldwide, is characterized by retinal ganglion cell (RGC) damage. NOP2/Sun RNA methyltransferase 4 (NSUN4), a known 5-methylcytosine (m5C) writer, is an essential dual-function mitochondrial protein that facilitates both the process of methylation and the coordination of mitoribosome assembly. However, few studies have focused on its role in RGCs. Methylated RNA immunoprecipitation sequencing (MeRIP-seq) combined with RNA sequencing (RNA-seq) was subsequently conducted to identify differences in the m5C methylome and gene expression profile in the N-methyl-d-aspartate (NMDA)-induced RGC injury model in vivo. We demonstrated that the significantly hypomethylated mRNAs were significantly enriched in the Sonic Hedgehog (SHH) signaling pathway in the NMDA group and that the mRNA expression of the m5C writer Nsun4 was downregulated. Subsequently, we examined the role of NSUN4 in R28 cells in response to glutamate stimulation. m5C dot blot and MeRIP (real-time fluorescence quantitative PCR) qPCR were employed to screen and validate the molecular mechanism of NSUN4 in glutamate-induced R28 cells through m5C regulation. Functionally, NSUN4 suppressed Ca2+ overload, mitochondrial dysfunction, and apoptosis of R28 cells in vitro. Mechanistically, NSUN4 increased the global mRNA m5C methylation level of Shh, GLI Family Zinc Finger Protein 1 (Gli1) and Gli2. Our study revealed that NSUN4 can alleviate the death of RGCs, which is associated with increased expression of Shh, Gli1 and Gli2 in the SHH signaling pathway in a m5C-dependent manner in R28 cells. Our findings provide new insights into potential biomarkers of retinal excitotoxity.

Publisher

Springer Science and Business Media LLC

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3