Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
University Research Facility in Chemical and Environmental Analysis, The Hong Kong Polytechnic University, Hong Kong, China.
Mol Neurobiol. 2019 Apr;56(4):2640-2652. doi: 10.1007/s12035-018-1238-y. Epub 2018 Jul 26.
Testis-specific protein, Y-encoded-like 2 (TSPYL2) is an X-linked gene in the locus for several neurodevelopmental disorders. We have previously shown that Tspyl2 knockout mice had impaired learning and sensorimotor gating, and TSPYL2 facilitates the expression of Grin2a and Grin2b through interaction with CREB-binding protein. To identify other genes regulated by TSPYL2, here, we showed that Tspyl2 knockout mice had an increased level of H3K27 trimethylation (H3K27me3) in the hippocampus, and TSPYL2 interacted with the H3K27 methyltransferase enhancer of zeste 2 (EZH2). We performed chromatin immunoprecipitation (ChIP)-sequencing in primary hippocampal neurons and divided all Refseq genes by k-mean clustering into four clusters from highest level of H3K27me3 to unmarked. We confirmed that mutant neurons had an increased level of H3K27me3 in cluster 1 genes, which consist of known EZH2 target genes important in development. We detected significantly reduced expression of genes including Gbx2 and Prss16 from cluster 1 and Acvrl1, Bdnf, Egr3, Grin2c, and Igf1 from cluster 2 in the mutant. In support of a dynamic role of EZH2 in repressing marked synaptic genes, the specific EZH2 inhibitor GSK126 significantly upregulated, while the demethylase inhibitor GSKJ4 downregulated the expression of Egr3 and Grin2c. GSK126 also upregulated the expression of Bdnf in mutant primary neurons. Finally, ChIP showed that hemagglutinin-tagged TSPYL2 co-existed with EZH2 in target promoters in neuroblastoma cells. Taken together, our data suggest that TSPYL2 is recruited to promoters of specific EZH2 target genes in neurons, and enhances their expression for proper neuronal maturation and function.
Y 编码样蛋白 2(TSPYL2)是 X 连锁基因,位于多个神经发育障碍的基因座上。我们之前已经表明,Tspyl2 敲除小鼠的学习和感觉运动门控能力受损,并且 TSPYL2 通过与 CREB 结合蛋白相互作用促进 Grin2a 和 Grin2b 的表达。为了鉴定 TSPYL2 调节的其他基因,我们在这里表明,Tspyl2 敲除小鼠的海马体中 H3K27 三甲基化(H3K27me3)水平升高,并且 TSPYL2 与 H3K27 甲基转移酶增强子结合蛋白 2(EZH2)相互作用。我们在原代海马神经元中进行了染色质免疫沉淀(ChIP)测序,并通过 k-均值聚类将所有 Refseq 基因分为四个簇,从 H3K27me3 水平最高到无标记。我们证实,突变神经元在包含重要发育基因的已知 EZH2 靶基因的簇 1 基因中 H3K27me3 水平升高。我们在突变体中检测到簇 1 中包括 Gbx2 和 Prss16 以及簇 2 中的 Acvrl1、Bdnf、Egr3、Grin2c 和 Igf1 在内的基因表达显著降低。支持 EZH2 在抑制标记突触基因中的动态作用,特异性 EZH2 抑制剂 GSK126 显著上调,而去甲基化酶抑制剂 GSKJ4 下调 Egr3 和 Grin2c 的表达。GSK126 还上调突变体原代神经元中 Bdnf 的表达。最后,ChIP 显示,神经母细胞瘤细胞中,带有血凝素标签的 TSPYL2 与 EZH2 共同存在于靶启动子上。总之,我们的数据表明,TSPYL2 被招募到神经元中特定 EZH2 靶基因的启动子上,并增强它们的表达以促进神经元成熟和功能。