Aix Marseille University, CNRS, IBDM, Turing Center for Living Systems, Marseille, France.
Max Planck Institute of Biochemistry, Martinsried, Germany.
Elife. 2021 Jan 6;10:e63726. doi: 10.7554/eLife.63726.
Skeletal muscles are composed of gigantic cells called muscle fibers, packed with force-producing myofibrils. During development, the size of individual muscle fibers must dramatically enlarge to match with skeletal growth. How muscle growth is coordinated with growth of the contractile apparatus is not understood. Here, we use the large flight muscles to mechanistically decipher how muscle fiber growth is controlled. We find that regulated activity of core members of the Hippo pathway is required to support flight muscle growth. Interestingly, we identify Dlg5 and Slmap as regulators of the STRIPAK phosphatase, which negatively regulates Hippo to enable post-mitotic muscle growth. Mechanistically, we show that the Hippo pathway controls timing and levels of sarcomeric gene expression during development and thus regulates the key components that physically mediate muscle growth. Since Dlg5, STRIPAK and the Hippo pathway are conserved a similar mechanism may contribute to muscle or cardiomyocyte growth in humans.
骨骼肌由巨大的细胞组成,称为肌纤维,充满产生力的肌原纤维。在发育过程中,单个肌纤维的大小必须显著增大以与骨骼生长相匹配。肌肉生长如何与收缩装置的生长相协调尚不清楚。在这里,我们使用大型飞行肌肉来从机械上解析肌纤维生长是如何被控制的。我们发现 Hippo 通路的核心成员的调节活性对于支持飞行肌肉的生长是必需的。有趣的是,我们鉴定出 Dlg5 和 Slmap 是 STRIPAK 磷酸酶的调节因子,它负调控 Hippo 以促进有丝分裂后肌肉的生长。从机制上讲,我们表明 Hippo 通路在发育过程中控制着肌节基因表达的时间和水平,从而调节了物理介导肌肉生长的关键组成部分。由于 Dlg5、STRIPAK 和 Hippo 通路在进化上是保守的,因此类似的机制可能有助于人类的肌肉或心肌细胞生长。