Mantila Roosa Sara M, Turner Charles H, Liu Yunlong
Department of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.
Gene Regul Syst Bio. 2012;6:43-53. doi: 10.4137/GRSB.S8068. Epub 2012 Jan 17.
Bone responds with increased bone formation to mechanical loading, and the time course of bone formation after initiating mechanical loading is well characterized. However, the regulatory activities governing the loading-dependent changes in gene expression are not well understood. The goal of this study was to identify the time-dependent regulatory mechanisms that governed mechanical loading-induced gene expression in bone using a predictive bioinformatics algorithm. A standard model for bone loading in rodents was employed in which the right forelimb was loaded axially for three minutes per day, while the left forearm served as a non-loaded, contralateral control. Animals were subjected to loading sessions every day, with 24 hours between sessions. Ulnas were sampled at 11 time points, from 4 hours to 32 days after beginning loading. Using a predictive bioinformatics algorithm, we created a linear model of gene expression and identified 44 transcription factor binding motifs and 29 microRNA binding sites that were predicted to regulate gene expression across the time course. Known and novel transcription factor binding motifs were identified throughout the time course, as were several novel microRNA binding sites. These time-dependent regulatory mechanisms may be important in controlling the loading-induced bone formation process.
骨骼会通过增加骨形成来对机械负荷做出反应,并且在开始机械负荷后骨形成的时间进程已得到充分表征。然而,控制基因表达中负荷依赖性变化的调节活动尚未得到很好的理解。本研究的目的是使用一种预测性生物信息学算法来确定控制骨骼中机械负荷诱导基因表达的时间依赖性调节机制。采用了一种啮齿动物骨骼负荷的标准模型,其中右前肢每天轴向负荷三分钟,而左前臂作为未负荷的对侧对照。每天对动物进行负荷实验,两次实验之间间隔24小时。在开始负荷后的4小时至32天内的11个时间点采集尺骨样本。使用预测性生物信息学算法,我们创建了一个基因表达的线性模型,并确定了44个转录因子结合基序和29个微小RNA结合位点,这些被预测在整个时间进程中调节基因表达。在整个时间进程中鉴定出了已知和新的转录因子结合基序,以及几个新的微小RNA结合位点。这些时间依赖性调节机制可能在控制负荷诱导的骨形成过程中很重要。