Mizutani Akifumi, Matsuzaki Ayumi, Momoi Mariko Y, Fujita Eriko, Tanabe Yuko, Momoi Takashi
Division of Development, Department of Human Inherited Metabolic Disease, National Institute of Neuroscience, Ogawahigashi-machi 4-1-1, Kodaira, Tokyo 187-8502, Japan.
Biochem Biophys Res Commun. 2007 Feb 23;353(4):869-74. doi: 10.1016/j.bbrc.2006.12.130. Epub 2006 Dec 26.
Although a mutation (R553H) in the forkhead box (FOX)P2 gene is associated with speech/language disorder, little is known about the function of FOXP2 or its relevance to this disorder. In the present study, we identify the forkhead nuclear localization domains that contribute to the cellular distribution of FOXP2. Nuclear localization of FOXP2 depended on two distally separated nuclear localization signals in the forkhead domain. A truncated version of FOXP2 lacking the leu-zip, Zn2+ finger, and forkhead domains that was observed in another patient with speech abnormalities demonstrated an aggregated cytoplasmic localization. Furthermore, FOXP2 (R553H) mainly exhibited a cytoplasmic localization despite retaining interactions with nuclear transport proteins (importin alpha and beta). Interestingly, wild type FOXP2 promoted the transport of FOXP2 (R553H) into the nucleus. Mutant and wild type FOXP2 heterodimers in the nucleus or FOXP2 R553H in the cytoplasm may underlie the pathogenesis of the autosomal dominant speech/language disorder.
尽管叉头框(FOX)P2基因中的一个突变(R553H)与言语/语言障碍相关,但对于FOXP2的功能或其与该障碍的相关性却知之甚少。在本研究中,我们确定了有助于FOXP2细胞分布的叉头核定位结构域。FOXP2的核定位取决于叉头结构域中两个远距离分开的核定位信号。在另一名有言语异常的患者中观察到的缺少亮氨酸拉链、锌指和叉头结构域的FOXP2截短版本表现出聚集的细胞质定位。此外,FOXP2(R553H)尽管与核转运蛋白(输入蛋白α和β)保持相互作用,但主要表现为细胞质定位。有趣的是,野生型FOXP2促进了FOXP2(R553H)向细胞核的转运。细胞核中的突变型和野生型FOXP2异二聚体或细胞质中的FOXP2 R553H可能是常染色体显性言语/语言障碍发病机制的基础。