Methyltransferase 1-mediated tRNA N7-methylguanosine modification regulates dentin formation during tooth root development via p53 signaling

下调和上调 细胞生物学 生物 牙本质 牙髓(牙) 信号转导 分子生物学 基因 生物化学 牙科 医学
作者
Xinyan Gan,Kun He,Qiuchan Xiong,Rui Sheng,Kexin Lei,Shuang Jiang,Xiaoyu Yang,Yimeng Cai,Denghao Huang,Yu Shi,Ling Ye,Quan Yuan,Qiwen Li
出处
期刊:Journal of Bone and Mineral Research [Oxford University Press]
卷期号:40 (6): 813-823
标识
DOI:10.1093/jbmr/zjaf056
摘要

Abstract tRNA N7-methylguanosine (m7G) is one of the most abundant epigenetic modifications in mammals, which is catalyzed by the methyltransferase 1-WD repeat-containing protein 4 (METTL1-WDR4) complex. Missense mutations in WDR4 have been linked to primordial dwarfism, which shows severe craniofacial developmental deformities including small teeth, but the underlying molecular mechanisms remain elusive. In this study, we explore the effect of m7G modification on dentin formation during tooth root development. METTL1 was actively expressed in mice developing tooth roots, and its expression became undetectable after tooth root formation. Next, we generated Prrx1-Cre driven Mettl1 (Prrx1Cre;Mettl1fl/fl) conditional KO mice to delete Mettl1 in dental mesenchyme and explored its regulation during tooth development. Micro-computed tomography revealed that the roots of the mandibular first molar in Prrx1Cre;Mettl1fl/fl mice were shorter and smaller compared to littermate control, with a reduction in the width of dentin and pre-dentin in both the root area and the crown area. Wdr4R215L/R215L mice also exhibited tooth root shortening and dentin thinning, phenocopying the Prrx1Cre;Mettl1fl/fl mice. Moreover, METTL1-depleted human dental pulp cells (hDPCs) showed decreased ability of proliferation, migration, and odontogenic differentiation. RNA-seq revealed upregulation of the p53 signaling pathway and cell cycle arrest after deletion of Mettl1. The proliferation and odontogenic differentiation of METTL1-depleted hDPCs is partially rescued with pifithrin-α (PFT-α), a p53 signaling inhibitor. Taken together, our results demonstrate that loss of METTL1-mediated tRNA m7G modification impairs the proliferation and odontogenic differentiation of hDPCs via the p53 signaling pathway and affects the dentin formation during tooth root development, providing a novel epigenetic mechanism underlying small teeth.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
薛建伟完成签到,获得积分10
刚刚
Hello应助予秋采纳,获得10
1秒前
1秒前
Yang完成签到 ,获得积分10
1秒前
chnningji发布了新的文献求助10
2秒前
3秒前
4秒前
李明星完成签到,获得积分10
4秒前
5秒前
小满完成签到,获得积分10
5秒前
科研通AI6.4应助raze采纳,获得10
6秒前
背后夜柳应助南楼小阁主采纳,获得30
7秒前
大模型应助PhDL1采纳,获得10
7秒前
7秒前
李爱国应助Han采纳,获得10
7秒前
7秒前
俊逸千山完成签到,获得积分20
8秒前
8秒前
淡然的新晴应助s子采纳,获得20
8秒前
冷艳紫南完成签到,获得积分10
9秒前
沙雕荷包蛋完成签到,获得积分10
9秒前
korosi完成签到,获得积分10
9秒前
爱吃西瓜的海獭完成签到,获得积分10
9秒前
9秒前
重要元容完成签到,获得积分20
10秒前
和谐亦瑶完成签到,获得积分10
10秒前
李明星发布了新的文献求助10
11秒前
Owen应助钟沐晨采纳,获得10
11秒前
俊逸千山发布了新的文献求助10
11秒前
123完成签到,获得积分20
11秒前
wanci应助ALAI采纳,获得10
12秒前
lzy发布了新的文献求助10
12秒前
大个应助theinu采纳,获得10
12秒前
13秒前
13秒前
13秒前
重要元容发布了新的文献求助10
13秒前
14秒前
机场内的就是你完成签到,获得积分20
14秒前
干净的琦应助可可采纳,获得30
14秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Emmy Noether's Wonderful Theorem 1200
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
基于非线性光纤环形镜的全保偏锁模激光器研究-上海科技大学 800
Signals, Systems, and Signal Processing 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6412196
求助须知:如何正确求助?哪些是违规求助? 8231302
关于积分的说明 17469873
捐赠科研通 5465024
什么是DOI,文献DOI怎么找? 2887514
邀请新用户注册赠送积分活动 1864253
关于科研通互助平台的介绍 1702915