Chen Guozhen, Zhu Jing, Lv Tiewei, Wu Gang, Sun Huichao, Huang Xupei, Tian Jie
Department of Cardiology, The Children's Hospital of Chongqing Medical University, Chongqing, PR China.
J Biomed Sci. 2009 Feb 23;16(1):24. doi: 10.1186/1423-0127-16-24.
Histone acetyltransferases (HATs), p300 and cAMP response element binding protein (CREB)-binding protein (CBP) are two structurally related transcriptional co-activators that activate expression of many eukaryotic genes involved in cellular growth and signaling, muscle differentiation and embryogenesis. However, whether these proteins play important and different roles in mouse cardiogenesis is not clear. Here, we investigate the protein distributions and mRNA expression of the two HATs in embryonic and adult mouse heart during normal heart development by using immunohistochemical and RT-PCR techniques. The data from immunohistochemical experiments revealed that p300 was extensively present in nearly every region of the hearts from embryonic stages to the adulthood. However, no CBP expression was detected in embryonic hearts at day E7.5. CBP expression appeared at the later stages, and the distribution of CBP was less than that of p300. In the developmental hearts after E10.5, both for p300 and CBP, the mRNA expression levels reached a peak on day E10.5, and then were gradually decreased afterwards. These results reveal that both p300 and CBP are related to embryonic heart development. The dynamic expression patterns of these two enzymes during mouse heart development indicate that they may play an important role on heart development. However, there is a difference in spatiotemporal expression patterns between these two enzymes during heart development. The expression of p300 is earlier and more predominate, suggesting that p300 may play a more important role in embryonic heart development especially during cardiac precursor cell induction and interventricular septum formation.
组蛋白乙酰转移酶(HATs)、p300和环磷酸腺苷反应元件结合蛋白(CREB)结合蛋白(CBP)是两种结构相关的转录共激活因子,它们可激活许多参与细胞生长和信号传导、肌肉分化及胚胎发生的真核基因的表达。然而,这些蛋白质在小鼠心脏发生过程中是否发挥重要且不同的作用尚不清楚。在此,我们运用免疫组织化学和逆转录-聚合酶链反应(RT-PCR)技术,研究了这两种HATs在正常心脏发育过程中的胚胎和成年小鼠心脏中的蛋白质分布及mRNA表达。免疫组织化学实验数据显示,从胚胎期到成年期,p300广泛存在于心脏的几乎每个区域。然而,在胚胎期第7.5天的胚胎心脏中未检测到CBP表达。CBP表达出现在后期阶段,且其分布范围小于p300。在胚胎期第10.5天之后的发育心脏中,p300和CBP的mRNA表达水平均在第10.5天达到峰值,随后逐渐下降。这些结果表明,p300和CBP均与胚胎心脏发育相关。这两种酶在小鼠心脏发育过程中的动态表达模式表明它们可能在心脏发育中发挥重要作用。然而,在心脏发育过程中,这两种酶的时空表达模式存在差异。p300的表达更早且更占主导,这表明p300可能在胚胎心脏发育中,尤其是在心脏前体细胞诱导和室间隔形成过程中发挥更重要的作用。