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SETD2介导的H3K36me3修饰对于小鼠中Col11a2和Sema3e转录以维持牙本质形成至关重要。

H3K36me3 modification by SETD2 is essential for Col11a2 and Sema3e transcription to maintain dentinogenesis in mice.

作者信息

Niu Jiaxin, Fu Jing, Feng Hao, Han Jiahao, Chen Zhi, Yang Guobin, Yuan Guohua

机构信息

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan 430079, China.

Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan 430079, China.

出版信息

Development. 2025 Jul 15;152(14). doi: 10.1242/dev.204352. Epub 2025 Jul 14.

Abstract

Dentin is a major mineralized component of teeth generated by odontoblasts. Several types of histone methylation have been reported to play important roles in odontoblast differentiation and dentinogenesis. However, the role of methylation on histone 3 at lysine 36 (H3K36) remains enigmatic. Here, we demonstrate high expression of SETD2, a methyltransferase catalyzing the trimethylation of H3K36 (H3K36me3), in the odontoblast layer. In vitro knockdown experiments and in vivo observations of two conditional knockout mouse models reveal that SETD2 is essential for odontoblast differentiation and dentinogenesis. Integrated analyses of RNA sequencing and spike-in CUT&Tag sequencing data show that SETD2 is crucial for both H3K36me3 occupancy at the loci of Col11a2 and Sema3e and their transcription. Further experiments verify that COL11A2 and SEMA3E act upstream of AKT1 signaling, promoting odontoblastic differentiation. In vitro and in vivo activation of AKT1 using SC79 (an AKT activator) partially rescues the impaired odontoblast differentiation caused by Setd2 knockdown or deficiency. Therefore, our findings indicate that H3K36me3 mediated by SETD2 is essential for dentinogenesis by regulating the expression of Col11a2 and Sema3e and AKT1 signaling.

摘要

牙本质是成牙本质细胞生成的牙齿主要矿化成分。据报道,几种组蛋白甲基化在成牙本质细胞分化和牙本质形成中发挥重要作用。然而,组蛋白H3赖氨酸36(H3K36)甲基化的作用仍不清楚。在此,我们证明了甲基转移酶SETD2(催化H3K36三甲基化(H3K36me3))在成牙本质细胞层中高表达。体外敲低实验以及对两种条件性敲除小鼠模型的体内观察表明,SETD2对成牙本质细胞分化和牙本质形成至关重要。RNA测序和掺入式CUT&Tag测序数据的综合分析表明,SETD2对于Col11a2和Sema3e基因座处的H3K36me3占据及其转录至关重要。进一步实验证实,COL11A2和SEMA3E在AKT1信号上游起作用,促进成牙本质细胞分化。使用SC79(一种AKT激活剂)在体外和体内激活AKT1可部分挽救由Setd2敲低或缺陷引起的成牙本质细胞分化受损。因此,我们的研究结果表明,SETD2介导的H3K36me3通过调节Col11a2和Sema3e的表达以及AKT1信号传导对牙本质形成至关重要。

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