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Regulatory Mechanisms in Bone Following Mechanical Loading

机译:机械负荷后骨骼的调节机制

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摘要

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.
机译:骨骼对机械负荷的骨骼形成反应增加,并且开始机械负荷后骨骼形成的时间过程已得到很好的表征。然而,调控基因表达中的负荷依赖性变化的调节活性尚不十分清楚。这项研究的目的是使用预测性生物信息学算法,确定时间依赖性调节机制,该机制控制骨骼中机械负荷诱导的基因表达。使用啮齿动物的骨负荷标准模型,其中右前肢每天轴向负荷3分钟,而左前臂作为无负荷对侧对照。每天对动物进行两次负荷训练,每次训练之间间隔24小时。开始加载后的4小时至32天的11个时间点对Ulnas进行了采样。使用预测性生物信息学算法,我们创建了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microRNA结合位点,预计它们将在整个时间过程中调节基因表达。在整个时间过程中,已知的和新颖的转录因子结合基序以及几个新颖的microRNA结合位点都得到了识别。这些与时间有关的调节机制在控制负荷诱导的骨形成过程中可能很重要。

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