Gutmann D H, Haipek C A, Burke S P, Sun C X, Scoles D R, Pulst S M
Department of Neurology, Washington University School of Medicine, Box 8111, 660 South Euclid Avenue, St Louis, MO 63110, USA.
Hum Mol Genet. 2001 Apr 1;10(8):825-34. doi: 10.1093/hmg/10.8.825.
The neurofibromatosis 2 tumor suppressor protein, merlin or schwannomin, functions as a negative growth regulator; however, its mechanism of action is not known. In an effort to determine how merlin regulates cell growth, we analyzed a recently identified novel merlin interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS). We demonstrate that regulated overexpression of HRS in rat schwannoma cells results in similar effects as overexpression of merlin, including growth inhibition, decreased motility and abnormalities in cell spreading. Previously, we showed that merlin forms an intramolecular association between the N- and C-termini and exists in "open" and "closed" conformations. Merlin interacts with HRS in the unfolded, or open, conformation. This HRS binding domain maps to merlin residues 453-557. Overexpression of C-terminal merlin has no effect on HRS function, arguing that merlin binding to HRS does not negatively regulate HRS growth suppressor activity. These results suggest the possibility that merlin and HRS may regulate cell growth in schwannoma cells through interacting pathways.
神经纤维瘤病2型肿瘤抑制蛋白,即默林蛋白或雪旺瘤蛋白,作为一种负性生长调节因子发挥作用;然而,其作用机制尚不清楚。为了确定默林蛋白如何调节细胞生长,我们分析了最近鉴定出的一种新型默林蛋白相互作用分子,即肝细胞生长因子调节的酪氨酸激酶底物(HRS)。我们证明,在大鼠雪旺瘤细胞中HRS的调控性过表达产生与默林蛋白过表达相似的效应,包括生长抑制、运动性降低以及细胞铺展异常。此前,我们表明默林蛋白在N端和C端之间形成分子内缔合,并以“开放”和“封闭”构象存在。默林蛋白在未折叠或开放构象下与HRS相互作用。这个HRS结合结构域定位于默林蛋白的453 - 557位残基。C端默林蛋白的过表达对HRS功能没有影响,这表明默林蛋白与HRS的结合不会负向调节HRS的生长抑制活性。这些结果提示,默林蛋白和HRS可能通过相互作用的途径调节雪旺瘤细胞中的细胞生长。