Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.
Epigenetics. 2011 Apr;6(4):405-9. doi: 10.4161/epi.6.4.14791. Epub 2011 Apr 1.
We have investigated promoter methylation of the Insr, Igf1 and Igf1r genes in skeletal and cardiac muscles of normal and diabetic db/db mice. No differences in Insr promoter methylation were found in the heart and skeletal muscles and no methylation was detected in the Igf1 promoter in skeletal muscle. In skeletal muscle, db/db males exhibited a 7.4-fold increase in Igf1r promoter methylation, which was accompanied by a 1.8-fold decrease in Igf1r mRNA levels, compared with controls. More than 50% of the detected methylation events were concentrated within an 18 bp sequence that includes one of the Sp1 binding sites. We conclude that the methylation level and pattern of the Igf1r promoter in skeletal muscle is related to gender and the diabetic state.
我们研究了正常和糖尿病 db/db 小鼠骨骼肌和心肌中 Insr、Igf1 和 Igf1r 基因的启动子甲基化。在心脏和骨骼肌中未发现 Insr 启动子甲基化的差异,在骨骼肌中也未检测到 Igf1 启动子的甲基化。与对照组相比,db/db 雄性小鼠的 Igf1r 启动子甲基化增加了 7.4 倍,同时 Igf1r mRNA 水平降低了 1.8 倍。超过 50%的检测到的甲基化事件集中在包含一个 Sp1 结合位点的 18 个碱基对序列内。我们得出结论,骨骼肌中 Igf1r 启动子的甲基化水平和模式与性别和糖尿病状态有关。