Suzuki Toshimitsu, Miyamoto Hiroyuki, Nakahari Takashi, Inoue Ikuyo, Suemoto Takahiro, Jiang Bin, Hirota Yuki, Itohara Shigeyoshi, Saido Takaomi C, Tsumoto Tadaharu, Sawamoto Kazunobu, Hensch Takao K, Delgado-Escueta Antonio V, Yamakawa Kazuhiro
Laboratory for Neurogenetics, RIKEN Brain Science Institute (BSI), Wako-shi, 351-0198 Saitama, Japan.
Hum Mol Genet. 2009 Mar 15;18(6):1099-109. doi: 10.1093/hmg/ddp006. Epub 2009 Jan 15.
Mutations in EFHC1 gene have been previously reported in patients with epilepsies, including those with juvenile myoclonic epilepsy. Myoclonin1, also known as mRib72-1, is encoded by the mouse Efhc1 gene. Myoclonin1 is dominantly expressed in embryonic choroid plexus, post-natal ependymal cilia, tracheal cilia and sperm flagella. In this study, we generated viable Efhc1-deficient mice. Most of the mice were normal in outward appearance, and both sexes were found to be fertile. However, the ventricles of the brains were significantly enlarged in the null mutants, but not in the heterozygotes. Although the ciliary structure was found intact, the ciliary beating frequency was significantly reduced in null mutants. In adult stages, both the heterozygous and null mutants developed frequent spontaneous myoclonus. Furthermore, the threshold of seizures induced by pentylenetetrazol was significantly reduced in both heterozygous and null mutants. These observations seem to further suggest that decrease or loss of function of myoclonin1 may be the molecular basis for epilepsies caused by EFHC1 mutations.
此前已有报道称,癫痫患者(包括青少年肌阵挛性癫痫患者)的EFHC1基因存在突变。肌阵挛蛋白1(Myoclonin1),也称为mRib72 - 1,由小鼠Efhc1基因编码。肌阵挛蛋白1在胚胎脉络丛、出生后室管膜纤毛、气管纤毛和精子鞭毛中呈显性表达。在本研究中,我们培育出了存活的Efhc1基因缺陷小鼠。大多数小鼠外观正常,且雌雄均具有生育能力。然而,基因敲除突变体小鼠的脑室显著增大,而杂合子小鼠则没有。虽然发现纤毛结构完整,但基因敲除突变体小鼠的纤毛摆动频率显著降低。在成年阶段,杂合子和基因敲除突变体小鼠均出现频繁的自发性肌阵挛。此外,杂合子和基因敲除突变体小鼠对戊四氮诱导癫痫发作的阈值均显著降低。这些观察结果似乎进一步表明,肌阵挛蛋白1功能的降低或丧失可能是EFHC1基因突变导致癫痫的分子基础。