Li Shuo, Luo Xiao-Mei, Peng Bo-Hui, Yang Chang-Jian, Peng Chang
Department of Pediatrics, Affiliated Hospital of Zunyi Medical College, Zunyi, Guizhou 563000, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Nov;20(11):950-954. doi: 10.7499/j.issn.1008-8830.2018.11.014.
To study the interactive regulatory effect of histone acetylation and methylation on cardiomyogenesis, and to provide a theoretical basis for the prevention and treatment of congenital heart disease.
A total of 24 Kunming mice were randomly divided into embryo day 14.5 (ED 14.5) group, embryo day 16.5 (ED 16.5) group, postnatal day 0.5 (PND 0.5) group, and postnatal day 7 (PND 7) group, with 6 mice in each group, and the heart tissue of fetal and neonatal mice was collected. Colorimetry was used to measure the activities of histone acetylases (HATs) and histone methyltransferases (HMTs) in the myocardium. Western blot was used to measure the expression of H3K9ac and H3K9me3 in the myocardium.
Colorimetry showed that the activities of HATs and HMTs were higher before birth and were lower after birth. There was a significant difference in the activity of HATs in the myocardium between the PND 0.5 and PND 7 groups and the ED 14.5 group (P<0.05), as well as between the PND 7 group and the ED 16.5 group (P<0.05). There was also a significant difference in the activity of HMTs in the myocardium between the PND 7 group and the ED 14.5 and ED 16.5 groups (P<0.05). Western blot showed higher expression of H3K9ac and H3K9me3 before birth and lower expression of H3K9ac and H3K9me3 after birth, and there were significant differences in the expression H3K9ac and H3K9me3 in the myocardium between the PND 0.5 and PND 7 groups and the ED 14.5 and ED 16.5 groups (P<0.05).
The dynamic expression of HATs, HMTs, H3K9ac, and H3K9me3 is observed during cardiomyogenesis, suggesting that histone H3K9ac acetylation and histone H3K9me3 methylation mediated by HATs and HMTs may play a role in interactive regulation during cardiomyogenesis.
研究组蛋白乙酰化和甲基化对心肌生成的交互调节作用,为先天性心脏病的防治提供理论依据。
将24只昆明小鼠随机分为胚胎第14.5天(ED 14.5)组、胚胎第16.5天(ED 16.5)组、出生后第0.5天(PND 0.5)组和出生后第7天(PND 7)组,每组6只,收集胎鼠和新生鼠的心脏组织。采用比色法检测心肌中组蛋白乙酰转移酶(HATs)和组蛋白甲基转移酶(HMTs)的活性。采用蛋白质免疫印迹法检测心肌中H3K9ac和H3K9me3的表达。
比色法显示,HATs和HMTs的活性在出生前较高,出生后较低。PND 0.5组和PND 7组与ED 14.5组心肌中HATs的活性有显著差异(P<0.05),PND 7组与ED 16.5组也有显著差异(P<0.05)。PND 7组与ED 14.5组和ED 16.5组心肌中HMTs的活性也有显著差异(P<0.05)。蛋白质免疫印迹法显示,H3K9ac和H3K9me3的表达在出生前较高,出生后较低,PND 0.5组和PND 7组与ED 14.5组和ED 16.5组心肌中H3K9ac和H3K9me3的表达有显著差异(P<0.05)。
在心肌生成过程中观察到HATs、HMTs、H3K9ac和H3K9me3的动态表达,提示由HATs和HMTs介导的组蛋白H3K9ac乙酰化和组蛋白H3K9me3甲基化可能在心肌生成的交互调节中发挥作用。