Ross Jason A, Barrett Brianna, Bensimon Victoria, Shukla Girish, Weyman Crystal M
Center for Gene Regulation in Health and Disease, Department of Biological, Geological, and Environmental Sciences, Cleveland State University, Cleveland, OH, US.
J Mol Signal. 2020 May 8;14:1. doi: 10.5334/1750-2187-14-1.
We have previously reported that stable expression of a dominant negative Death Receptor 5 (dnDR5) in skeletal myoblasts results in decreased basal caspase activity and decreased mRNA and protein expression of the muscle regulatory transcription factor MyoD in growth medium (GM), resulting in inhibited differentation when myoblasts are then cultured in differentiation media (DM). Further, this decreased level of MyoD mRNA was not a consequence of altered message stability, but rather correlated with decreased acetylation of histones in the distal regulatory region (DRR) of the MyoD extended promoter known to control MyoD transcription. As serum response factor (SRF) is the transcription factor known to be responsible for basal MyoD expression in GM, we compared the level of SRF binding to the non-canonical serum response element (SRE) within the DRR in parental and dnDR5 expressing myoblasts. Herein, we report that stable expression of dnDR5 resulted in decreased levels of serum response factor (SRF) binding to the CArG box in the SRE of the DRR. Total SRF expression levels were not affected, but phosphorylation indicative of SRF activation was impaired. This decreased SRF phosphorylation correlated with decreased phosphorylation-induced activation of p38 kinase. Moreover, the aforementioned signaling events affected by expression of dnDR5 could be appropriately recapitulated using either a pharmacological inhibitor of caspase 3 or p38 kinase. Thus, our results have established a signaling pathway from DR5 through caspases to p38 kinase activation, to SRF activation and the basal expression of MyoD.
我们之前报道过,在骨骼肌成肌细胞中稳定表达显性负性死亡受体5(dnDR5)会导致基础半胱天冬酶活性降低,并且在生长培养基(GM)中肌肉调节转录因子MyoD的mRNA和蛋白质表达减少,从而在成肌细胞随后在分化培养基(DM)中培养时抑制分化。此外,MyoD mRNA水平的降低不是信息稳定性改变的结果,而是与已知控制MyoD转录的MyoD延伸启动子远端调节区域(DRR)中组蛋白乙酰化减少相关。由于血清反应因子(SRF)是已知负责GM中基础MyoD表达的转录因子,我们比较了亲本和成肌细胞中表达dnDR5的细胞中SRF与DRR内非经典血清反应元件(SRE)结合的水平。在此,我们报道dnDR5的稳定表达导致血清反应因子(SRF)与DRR的SRE中CArG框的结合水平降低。总SRF表达水平不受影响,但指示SRF激活的磷酸化受损。这种SRF磷酸化的降低与p38激酶磷酸化诱导的激活减少相关。此外,使用半胱天冬酶3或p38激酶的药理学抑制剂可以适当重现受dnDR5表达影响的上述信号事件。因此,我们的结果建立了一条从DR5通过半胱天冬酶到p38激酶激活、再到SRF激活和MyoD基础表达的信号通路。