SUBCELLULAR MRNA DISTRIBUTION IN MYOCYTES

我们的长期研究目标是了解横纹肌如何适应其分子组成，以响应改变的生理需求。本项目探讨机械工作、细胞内信号和蛋白质合成局部控制之间的联系。总的假设是，机械应变是控制翻译和区域蛋白质合成的主要生理信号。具体目标展示机械负荷如何通过调节α - myhc mRNA的3'UTR与mRNA结合蛋白之间的相互作用来调节翻译。我们期望发现机械活动触发特定的细胞内信号通路。我们提出特异性mrbf的磷酸化调节它们与α - myhc 3'UTR上特定顺式序列的结合，从而控制翻译。具体目标2。表明机械负荷通过α - myhc mRNA的3'UTR调控定位，导致局部蛋白质合成。我们期望发现机械应变的方向影响肌肉细胞的生长方向，纵向应变在细胞末端产生mRNA定位，而横向染色在肌纤维间产生定位。我们期望这种空间分布是由3'UTR控制的。细胞重塑的控制对于增加心脏的机械输出很重要，这可能是运动时的健康反应，也可能是心力衰竭时的病理反应。

Our long-term research goal is to understand how striated muscle adapts its molecular composition in response to altered physiological demand. This project explores the link between mechanical work, intracellular signals and local control of protein synthesis. The overall hypothesis is that mechanical strain is a primary physiological signal that controls translation and regional protein synthesis. Specific Aim 1. To show how mechanical load regulates translation by modulation of the interaction between the 3'UTR of alpha-MyHC mRNA and mRNA binding proteins. We expect to find that mechanical activity triggers a specific intracellular signaling pathway. We propose that phosphorylation of specific mRBFs modulates their binding to a specific cis-sequence on the alpha-MyHC 3'UTR, thus controlling translation. Specific Aim 2. To show that mechanical load regulates localization via the 3'UTR of alpha-MyHC mRNA leading to local protein synthesis. We expect to find that the direction of mechanical strain influences the direction of growth of the muscle cell with the longitudinal strain producing mRNA localization at the ends of the cells while transverse stain produces inter-myofibrillar localization. We expect that this spatial distribution is governed by the 3'UTR. Control of cell remodeling is important for increasing the mechanical output of the heart that can be a healthy response in exercise or pathological in heart failure.