Ogura Yoji, Miyake Noriko, Kou Ikuyo, Iida Aritoshi, Nakajima Masahiro, Takeda Kazuki, Fujibayashi Shunsuke, Shiina Masaaki, Okada Eijiro, Toyama Yoshiaki, Iwanami Akio, Ishii Ken, Ogata Kazuhiro, Asahara Hiroshi, Matsumoto Naomichi, Nakamura Masaya, Matsumoto Morio, Ikegawa Shiro
Laboratory of Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences, Tokyo, 108-8639, Japan.
Department of Orthopaedic Surgery, School of Medicine, Keio University, Tokyo, 160-8582, Japan.
PLoS One. 2015 Nov 6;10(11):e0142126. doi: 10.1371/journal.pone.0142126. eCollection 2015.
Spinal extradural arachnoid cyst (SEDAC) is a cyst in the spinal canal that protrudes into the epidural space from a defect in the dura mater and leads to neurological disturbances. We previously showed that familial SEDAC is caused by FOXC2 mutation; however, the causal gene of sporadic SEDAC has not been identified. To identify the causal gene of sporadic SEDAC, we performed whole exome sequencing for 12 subjects with sporadic SEDAC and identified heterozygous HOXD4 loss-of-function mutations in three subjects. HOXD4 haplo-insufficiency causes SEDAC and a transcriptional network containing HOXD4 and FOXC2 is involved in the development of the dura mater and the etiology of SEDAC.
脊髓硬膜外蛛网膜囊肿(SEDAC)是一种位于椎管内的囊肿,它从硬脑膜的缺损处突入硬膜外间隙并导致神经功能障碍。我们之前表明,家族性SEDAC是由FOXC2突变引起的;然而,散发性SEDAC的致病基因尚未确定。为了确定散发性SEDAC的致病基因,我们对12名散发性SEDAC患者进行了全外显子组测序,并在3名患者中鉴定出杂合的HOXD4功能丧失突变。HOXD4单倍体不足导致SEDAC,并且一个包含HOXD4和FOXC2的转录网络参与硬脑膜的发育和SEDAC的病因学。