骨在机械负荷后的调节机制。

Gene regulation and systems biology Pub Date : 2012-01-01 Epub Date: 2012-01-17 DOI:10.4137/GRSB.S8068
Sara M Mantila Roosa, Charles H Turner, Yunlong Liu
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引用次数: 14

摘要

骨对机械载荷的反应是增加骨形成,并且在开始机械载荷后骨形成的时间过程是很有特征的。然而,调控负荷依赖性基因表达变化的调控活动尚不清楚。本研究的目的是使用预测性生物信息学算法确定控制骨中机械负荷诱导的基因表达的时间依赖性调节机制。采用标准的啮齿动物骨负荷模型,右前肢每天轴向负荷3分钟,而左前臂作为非负荷的对侧对照。动物每天都要进行加载,每次之间间隔24小时。在开始加载后4小时至32天的11个时间点对尺骨进行采样。使用预测生物信息学算法,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,这些位点被预测在整个时间过程中调节基因表达。已知的和新的转录因子结合基序在整个时间过程中被确定,以及几个新的microRNA结合位点。这些时间依赖性的调节机制在控制负荷诱导的骨形成过程中可能是重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulatory mechanisms in bone following mechanical loading.

Regulatory mechanisms in bone following mechanical loading.

Regulatory mechanisms in bone following mechanical loading.

Regulatory mechanisms in bone following mechanical loading.

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.

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