Shimizu Toshiyuki, Seto Azusa, Maita Nobuo, Hamada Keisuke, Tsukita Shoichiro, Tsukita Sachiko, Hakoshima Toshio
Structural Biology Laboratory, Nara Institute of Science and Technology and CREST, Japan.
J Biol Chem. 2002 Mar 22;277(12):10332-6. doi: 10.1074/jbc.M109979200. Epub 2001 Dec 27.
Neurofibromatosis type 2 (NF2) is a dominantly inherited disease associated with the central nervous system. The NF2 gene product merlin is a tumor suppressor, and its mutation or inactivation causes this disease. We report here the crystal structure of the merlin FERM domain containing a 22-residue alpha-helical segment. The structure reveals that the merlin FERM domain consists of three subdomains displaying notable features of the electrostatic surface potentials, although the overall surface potentials similar to those of ezrin/radixin/moesin (ERM) proteins indicate electrostatic membrane association. The structure also is consistent with inactivation mechanisms caused by the pathogenic mutations associated with NF2.
2型神经纤维瘤病(NF2)是一种与中枢神经系统相关的显性遗传病。NF2基因产物默林是一种肿瘤抑制因子,其突变或失活会导致这种疾病。我们在此报告包含一个22个残基α螺旋片段的默林FERM结构域的晶体结构。该结构表明,默林FERM结构域由三个亚结构域组成,这些亚结构域显示出静电表面电位的显著特征,尽管其整体表面电位与埃兹蛋白/根蛋白/膜突蛋白(ERM)相似,表明存在静电膜结合。该结构也与NF2相关致病突变引起的失活机制一致。