Fielitz Jens, Kim Mi-Sung, Shelton John M, Latif Shuaib, Spencer Jeffrey A, Glass David J, Richardson James A, Bassel-Duby Rhonda, Olson Eric N
Department of Molecular Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9148, USA.
J Clin Invest. 2007 Sep;117(9):2486-95. doi: 10.1172/JCI32827.
Maintenance of skeletal and cardiac muscle structure and function requires precise control of the synthesis, assembly, and turnover of contractile proteins of the sarcomere. Abnormalities in accumulation of sarcomere proteins are responsible for a variety of myopathies. However, the mechanisms that mediate turnover of these long-lived proteins remain poorly defined. We show that muscle RING finger 1 (MuRF1) and MuRF3 act as E3 ubiquitin ligases that cooperate with the E2 ubiquitin-conjugating enzymes UbcH5a, -b, and -c to mediate the degradation of beta/slow myosin heavy chain (beta/slow MHC) and MHCIIa via the ubiquitin proteasome system (UPS) in vivo and in vitro. Accordingly, mice deficient for MuRF1 and MuRF3 develop a skeletal muscle myopathy and hypertrophic cardiomyopathy characterized by subsarcolemmal MHC accumulation, myofiber fragmentation, and diminished muscle performance. These findings identify MuRF1 and MuRF3 as key E3 ubiquitin ligases for the UPS-dependent turnover of sarcomeric proteins and reveal a potential basis for myosin storage myopathies.
维持骨骼肌和心肌的结构与功能需要精确控制肌节收缩蛋白的合成、组装及更新。肌节蛋白积累异常会导致多种肌病。然而,介导这些长寿蛋白更新的机制仍不清楚。我们发现肌肉环状指蛋白1(MuRF1)和MuRF3作为E3泛素连接酶,在体内和体外与E2泛素结合酶UbcH5a、-b和-c协同作用,通过泛素蛋白酶体系统(UPS)介导β/慢肌球蛋白重链(β/慢MHC)和MHCIIa的降解。相应地,缺乏MuRF1和MuRF3的小鼠会出现骨骼肌肌病和肥厚性心肌病,其特征为肌膜下MHC积累、肌纤维断裂和肌肉功能减退。这些发现确定MuRF1和MuRF3是UPS依赖性肌节蛋白更新的关键E3泛素连接酶,并揭示了肌球蛋白贮积性肌病的潜在基础。