Surace Ezequiel I, Haipek Carrie A, Gutmann David H
Department of Neurology, Washington University School of Medicine, Box 8111, 660 S Euclid Avenue, St Louis, MO 63110, USA.
Oncogene. 2004 Jan 15;23(2):580-7. doi: 10.1038/sj.onc.1207142.
The neurofibromatosis 2 (NF2) tumor suppressor gene product, merlin, belongs to the ezrin-radixin-moesin (ERM) subgroup of the Protein 4.1 family, which links cell surface glycoproteins to the actin cytoskeleton. Previous studies have suggested that phosphorylation of merlin, similar to other ERM proteins, may regulate its function. To determine whether merlin phosphorylation has functional consequences for merlin suppression of cell growth and motility, we generated doxycycline-regulatable RT4 schwannoma cell lines that inducibly express full-length merlin with mutations at two potential phosphorylation sites (amino-acid residues S518 and T576). Whereas a mutation at S518 that mimics constitutive phosphorylation (S518D) abrogates the ability of merlin to suppress cell growth and motility, the S518A merlin mutant, which mimics nonphosphorylated merlin, functions equivalently to wild-type merlin. Similar mutations involving T576, the analogous phosphorylation site in ERM proteins important for regulating their function, had no effect. In contrast to other functionally inactive missense merlin mutants, the regulated overexpression of S518D merlin resulted in dramatic changes in cell shape and the elaboration of filopodial extensions. These results provide the first direct demonstration that the S518D merlin mutation, which mimics merlin phosphorylation, impairs not only merlin growth and motility suppression but also leads to an acquisition of a novel phenotype previously ascribed to ERM proteins.
神经纤维瘤病2型(NF2)肿瘤抑制基因产物默林(merlin)属于4.1蛋白家族的埃兹蛋白-根蛋白-膜突蛋白(ERM)亚组,该亚组将细胞表面糖蛋白与肌动蛋白细胞骨架相连。先前的研究表明,与其他ERM蛋白类似,默林的磷酸化可能调节其功能。为了确定默林磷酸化对默林抑制细胞生长和运动是否具有功能性影响,我们构建了强力霉素可调控的RT4雪旺氏细胞瘤细胞系,该细胞系可诱导表达在两个潜在磷酸化位点(氨基酸残基S518和T576)发生突变的全长默林。模拟组成型磷酸化的S518位点突变(S518D)消除了默林抑制细胞生长和运动的能力,而模拟非磷酸化默林的S518A默林突变体的功能与野生型默林相当。涉及T576(ERM蛋白中对调节其功能很重要的类似磷酸化位点)的类似突变没有影响。与其他功能失活的错义默林突变体不同,S518D默林的调控过表达导致细胞形态发生显著变化并形成丝状伪足样延伸。这些结果首次直接证明,模拟默林磷酸化的S518D默林突变不仅损害默林对生长和运动的抑制,还导致获得一种先前归因于ERM蛋白的新表型。