Sadayappan Sakthivel, Osinska Hanna, Klevitsky Raisa, Lorenz John N, Sargent Michelle, Molkentin Jeffrey D, Seidman Christine E, Seidman Jonathan G, Robbins Jeffrey
Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16918-23. doi: 10.1073/pnas.0607069103. Epub 2006 Oct 30.
Cardiac myosin binding protein C (cMyBP-C) has three phosphorylatable serines at its N terminus (Ser-273, Ser-282, and Ser-302), and the residues' phosphorylation states may alter thick filament structure and function. To examine the effects of cMyBP-C phosphorylation, we generated transgenic mice with cardiac-specific expression of a cMyBP-C in which the three phosphorylation sites were mutated to aspartic acid, mimicking constitutive phosphorylation (cMyBP-C(AllP+)). The allele was bred into a cMyBP-C null background (cMyBP-C((t/t))) to ensure the absence of endogenous dephosphorylated cMyBP-C. cMyBP-C(AllP+) was incorporated normally into the cardiac sarcomere and restored normal cardiac function in the null background. However, subtle changes in sarcomere ultrastructure, characterized by increased distances between the thick filaments, indicated that phosphomimetic cMyBP-C affects thick-thin filament relationships, and yeast two-hybrid data and pull-down studies both showed that charged residues in these positions effectively prevented interaction with the myosin heavy chain. Confirming the physiological relevance of these data, the cMyBP-C(AllP+:(t/t)) hearts were resistant to ischemia-reperfusion injury. These data demonstrate that cMyBP-C phosphorylation functions in maintaining thick filament spacing and structure and can help protect the myocardium from ischemic injury.
心肌肌球蛋白结合蛋白C(cMyBP-C)在其N端有三个可磷酸化的丝氨酸(Ser-273、Ser-282和Ser-302),这些残基的磷酸化状态可能会改变粗肌丝的结构和功能。为了研究cMyBP-C磷酸化的影响,我们构建了心脏特异性表达cMyBP-C的转基因小鼠,其中三个磷酸化位点突变为天冬氨酸,模拟组成型磷酸化(cMyBP-C(AllP+))。将该等位基因培育到cMyBP-C基因敲除背景(cMyBP-C((t/t)))中,以确保不存在内源性去磷酸化的cMyBP-C。cMyBP-C(AllP+)正常整合到心肌肌节中,并在基因敲除背景下恢复了正常心脏功能。然而,肌节超微结构的细微变化,表现为粗肌丝之间的距离增加,表明模拟磷酸化的cMyBP-C影响粗细肌丝的关系,酵母双杂交数据和下拉实验均表明这些位置的带电荷残基有效地阻止了与肌球蛋白重链的相互作用。cMyBP-C(AllP+:(t/t))心脏对缺血-再灌注损伤具有抗性,证实了这些数据的生理相关性。这些数据表明,cMyBP-C磷酸化在维持粗肌丝间距和结构方面发挥作用,并有助于保护心肌免受缺血损伤。