Epstein J A, Lam P, Jepeal L, Maas R L, Shapiro D N
Division of Cardiology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
J Biol Chem. 1995 May 19;270(20):11719-22. doi: 10.1074/jbc.270.20.11719.
Pax3 is an evolutionarily conserved transcription factor expressed in the lateral dermomyotome, a region that gives rise to limb muscle progenitors. Mutations in Pax-3 account for the mouse mutant Splotch which develops without limb musculature. We demonstrate that Pax3 can inhibit myogenic differentiation of C2C12 myoblasts normally induced by exposure to low serum. Specific missense mutations that affect the DNA binding characteristics of the two distinct DNA binding domains of Pax3 abolish this effect. Furthermore, we show that Pax3 can inhibit myogenic differentiation of 10T1/2 fibroblasts transfected with MyoD, but not of 10T1/2 cells transfected with myogenin. This anti-myogenic property is shared by a PAX3-forkhead fusion protein resulting from a t(2;13) chromosomal translocation found in pediatric alveolar rhabdomyosarcomas. These results suggest that Pax3 may suppress the terminal differentiation of migrating limb myoblasts and that the PAX3-forkhead fusion may contribute to the phenotype of alveolar rhabdomyosarcoma by preventing terminal differentiation.
Pax3是一种在进化上保守的转录因子,在外侧生皮节中表达,该区域产生肢体肌肉祖细胞。Pax - 3的突变导致小鼠突变体斑点(Splotch)的出现,该突变体在发育过程中没有肢体肌肉组织。我们证明,Pax3可以抑制通常由低血清诱导的C2C12成肌细胞的肌源性分化。影响Pax3两个不同DNA结合域的DNA结合特性的特定错义突变消除了这种作用。此外,我们表明,Pax3可以抑制用MyoD转染的10T1/2成纤维细胞的肌源性分化,但不能抑制用肌细胞生成素转染的10T1/2细胞的肌源性分化。在儿童肺泡横纹肌肉瘤中发现的t(2;13)染色体易位产生的PAX-3-叉头融合蛋白也具有这种抗肌源性特性。这些结果表明,Pax3可能抑制迁移的肢体成肌细胞的终末分化,并且PAX3-叉头融合蛋白可能通过阻止终末分化而导致肺泡横纹肌肉瘤的表型。