已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

ALKBH5 Regulates Osteogenic Differentiation via the lncRNA/mRNA Complex

细胞生物学 信使核糖核酸 生物 化学 遗传学 基因
作者
Yan Song,Hu Gao,Yuxia Pan,Yuxi Gu,Wei Sun,Yajun Wang,Jun Liu
出处
期刊:Journal of Dental Research [SAGE Publishing]
卷期号:103 (11): 1119-1129 被引量:4
标识
DOI:10.1177/00220345241266775
摘要

Human adipose-derived stem cells (hASCs) are commonly used in bone tissue regeneration. The N6-methyladenosine (m 6 A) modification has emerged as a novel regulatory mechanism for gene expression, playing a critical role in osteogenic differentiation of stem cells. However, the precise role and mechanism of alkylation repair homolog 5 (ALKBH5) in hASC osteogenesis remain incompletely elucidated and warrant further investigation. Herein, we employed methylated RNA immunoprecipitation sequencing, RNA sequencing, and weighted gene coexpression network analysis to identify a key long noncoding RNA (lncRNA) in hASCs: lncRNA AK311120. Functional experiments demonstrated that lnc-AK311120 promoted the osteogenic differentiation of hASCs, while a mutation at the m 6 A central site A of lnc-AK311120 was found to decrease the level of m 6 A modification. The osteogenic effect of ALKBH5 was confirmed both in vitro and in vivo using a mandibular defect model in nude mice. Subsequent investigations revealed that knockdown of ALKBH5 resulted in a significant increase in the m 6 A modification level of lnc-AK311120, accompanied by a downregulation in the expression level of lnc-AK311120. Additional rescue experiments demonstrated that overexpression of lnc-AK311120 could restore the phenotype after ALKBH5 knockdown. We observed that AK311120 interacted with the RNA-binding proteins DExH-Box helicase 9 (DHX9) and YTH domain containing 2 (YTHDC2) to form a ternary complex, while mitogen-activated protein kinase kinase 7 (MAP2K7) served as the shared downstream target gene of DHX9 and YTHDC2. Knockdown of AK311120 led to a reduction in the binding affinity between DHX9/YTHDC2 and the target gene MAP2K7. Furthermore, ALKBH5 facilitated the translation of MAP2K7 and activated the downstream JNK signaling pathway through the AK311120–DHX9–YTHDC2 complex, without affecting its messenger RNA level. Collectively, we have investigated the regulatory effect and mechanism of ALKBH5-mediated demethylation of lncRNA in hASC osteogenesis for the first time, offering a promising approach for bone tissue engineering.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
ooooozhubi完成签到 ,获得积分10
1秒前
Symphony0完成签到 ,获得积分10
2秒前
不配.应助11125abe采纳,获得20
5秒前
于清绝完成签到 ,获得积分10
10秒前
NOTHING完成签到 ,获得积分10
11秒前
林狗完成签到 ,获得积分10
14秒前
阳光的凌雪完成签到 ,获得积分10
22秒前
流星完成签到,获得积分10
25秒前
完美梨愁完成签到 ,获得积分10
25秒前
洁净的诗珊完成签到 ,获得积分10
27秒前
bless完成签到 ,获得积分10
31秒前
Bin_Liu发布了新的文献求助10
34秒前
38秒前
量子星尘发布了新的文献求助10
41秒前
41秒前
CodeCraft应助香蕉秋柳采纳,获得10
42秒前
Splaink完成签到 ,获得积分10
44秒前
47秒前
jasmine完成签到,获得积分10
47秒前
ING完成签到,获得积分10
48秒前
Iris完成签到 ,获得积分10
49秒前
炙热初柔发布了新的文献求助10
50秒前
科研通AI6应助怡然尔白采纳,获得10
50秒前
传奇3应助。。。采纳,获得10
51秒前
迅速的幻雪完成签到 ,获得积分10
55秒前
56秒前
1分钟前
小炮仗完成签到 ,获得积分10
1分钟前
2877321934发布了新的文献求助10
1分钟前
orrrr发布了新的文献求助10
1分钟前
shuhaha完成签到,获得积分10
1分钟前
1分钟前
GT完成签到,获得积分10
1分钟前
1分钟前
开心蛋挞完成签到 ,获得积分10
1分钟前
qjw发布了新的文献求助10
1分钟前
超帅妙竹完成签到,获得积分20
1分钟前
不安愚志完成签到 ,获得积分10
1分钟前
阿龙啊完成签到 ,获得积分10
1分钟前
超帅妙竹发布了新的文献求助10
1分钟前
高分求助中
(禁止应助)【重要!!请各位详细阅读】【科研通的精品贴汇总】 10000
Organic Chemistry 1500
The Netter Collection of Medical Illustrations: Digestive System, Volume 9, Part III - Liver, Biliary Tract, and Pancreas (3rd Edition) 600
Introducing Sociology Using the Stuff of Everyday Life 400
Conjugated Polymers: Synthesis & Design 400
Picture Books with Same-sex Parented Families: Unintentional Censorship 380
Metals, Minerals, and Society 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4260974
求助须知:如何正确求助?哪些是违规求助? 3794031
关于积分的说明 11898626
捐赠科研通 3441361
什么是DOI,文献DOI怎么找? 1888651
邀请新用户注册赠送积分活动 939376
科研通“疑难数据库(出版商)”最低求助积分说明 844460