Nakagawa Osamu, Arnold Michael, Nakagawa Masayo, Hamada Hideaki, Shelton John M, Kusano Hajime, Harris Thomas M, Childs Geoffrey, Campbell Kevin P, Richardson James A, Nishino Ichizo, Olson Eric N
Department of Molecular Biology, The University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390, USA.
Genes Dev. 2005 Sep 1;19(17):2066-77. doi: 10.1101/gad.1338705.
Myocyte enhancer factor 2 (MEF2) plays essential roles in transcriptional control of muscle development. However, signaling pathways acting downstream of MEF2 are largely unknown. Here, we performed a microarray analysis using Mef2c-null mouse embryos and identified a novel MEF2-regulated gene encoding a muscle-specific protein kinase, Srpk3, belonging to the serine arginine protein kinase (SRPK) family, which phosphorylates serine/arginine repeat-containing proteins. The Srpk3 gene is specifically expressed in the heart and skeletal muscle from embryogenesis to adulthood and is controlled by a muscle-specific enhancer directly regulated by MEF2. Srpk3-null mice display a new entity of type 2 fiber-specific myopathy with a marked increase in centrally placed nuclei; while transgenic mice overexpressing Srpk3 in skeletal muscle show severe myofiber degeneration and early lethality. We conclude that normal muscle growth and homeostasis require MEF2-dependent signaling by Srpk3.
肌细胞增强因子2(MEF2)在肌肉发育的转录调控中发挥着重要作用。然而,MEF2下游的信号通路在很大程度上仍不清楚。在此,我们使用Mef2c基因缺失的小鼠胚胎进行了微阵列分析,并鉴定出一个新的MEF2调控基因,该基因编码一种肌肉特异性蛋白激酶Srpk3,它属于丝氨酸精氨酸蛋白激酶(SRPK)家族,可磷酸化含丝氨酸/精氨酸重复序列的蛋白质。Srpk3基因从胚胎发生到成年期在心脏和骨骼肌中特异性表达,并受MEF2直接调控的肌肉特异性增强子的控制。Srpk3基因缺失的小鼠表现出一种新的2型纤维特异性肌病,其中心核显著增加;而在骨骼肌中过表达Srpk3的转基因小鼠则表现出严重的肌纤维变性和早期致死性。我们得出结论,正常肌肉生长和体内平衡需要Srpk3介导的MEF2依赖性信号传导。