Hu Ke, Liu Lijing, Qian Hong, Zhou Ting, Li Yuxian, Yu Jiaxian, Tan Bifeng
Medical College, Hunan University of Medicine, Huaihua 418000, China.
Department of Cardiovascular Diseases, First Affiliated Hospital, Hunan University of Medicine, Huaihua 418000, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Dec;33(12):1610-1614.
Objective To screen the nucleus located-methyltransferase in murine macrophages (RAW246.7 cells) after peroxisome proliferator-activated receptors (PPAR) is activated by alpinetin so as to prove the epigenetic modification effect of alpinetin. Methods RAW246.7 cells were divided into control group, alpinetin group (final concentrations including 100, 200, 500, 1000 μg/mL) and 1000 μg/mL alpinetin combined with 0.1 mmol/mL GW9662 group. Firstly, bioinformatics database String was searched for the methyltransferases which might interact with PPAR. Then co-immunoprecipitation was used to screen the specific nucleus-located methyltransferase interacting with PPAR. Finally, the expressions of the related methyltransferases were validated by fluorescent quantitative PCR. Results Co-immunoprecipitation proved that EZH2, DNMT3α and TDG were the specific methyltransferases which interacted with the activated PPAR in the nucleus when induced by a certain concentration of alpinetin, which was basically consistent with the search result of the String database. No methyltransferase was found to interact with PPAR if GW9662 was added. Furthermore, only by a high concentration of alpinetin (1 000 μg/mL), could the synthesis of TDG mRNA be promoted, yet the synthesis of DNMT3α and EZH2 were not influenced. Conclusion Alpinetin, the PPAR activator, could promote the synthesis and interaction of specific methyltransferases with PPAR in the nucleus, which indicates that methylation modification on histone or cytosine may be the interpretation for the effect of gene expression regulation caused by alpinetin.
目的 筛选经山柰素激活过氧化物酶体增殖物激活受体(PPAR)后,小鼠巨噬细胞(RAW246.7细胞)中的核定位甲基转移酶,以证明山柰素的表观遗传修饰作用。方法 将RAW246.7细胞分为对照组、山柰素组(终浓度分别为100、200、500、1000μg/mL)和1000μg/mL山柰素+0.1mmol/mL GW9662组。首先,在生物信息学数据库String中搜索可能与PPAR相互作用的甲基转移酶。然后采用免疫共沉淀法筛选与PPAR相互作用的特异性核定位甲基转移酶。最后,通过荧光定量PCR验证相关甲基转移酶的表达。结果 免疫共沉淀证明,在一定浓度山柰素诱导下,EZH2、DNMT3α和TDG是与细胞核中活化的PPAR相互作用的特异性甲基转移酶,这与String数据库的搜索结果基本一致。加入GW9662后未发现有甲基转移酶与PPAR相互作用。此外,仅高浓度山柰素(1000μg/mL)可促进TDG mRNA的合成,而对DNMT3α和EZH2的合成无影响。结论 PPAR激活剂山柰素可促进细胞核中特异性甲基转移酶与PPAR的合成及相互作用,这表明组蛋白或胞嘧啶上的甲基化修饰可能是山柰素引起基因表达调控作用机制的解释。