Hirata Tsutomu, Nakazawa Masato, Yoshihara Sei-ichi, Miyachi Hitoshi, Kitamura Kunio, Yoshihara Yoshihiro, Hibi Masahiko
Laboratory for Vertebrate Axis Formation, Center for Developmental Biology, RIKEN, Kobe 650-0047, Japan.
Development. 2006 Apr;133(8):1433-43. doi: 10.1242/dev.02329. Epub 2006 Mar 15.
Fez is a zinc-finger gene encoding a transcriptional repressor that is expressed in the olfactory epithelium, hypothalamus, ventrolateral pallium and prethalamus at mid-gestation. To reveal its function, we generated Fez-deficient mice. The Fez-deficient mice showed several abnormalities in the olfactory system: (1) impaired axonal projection of the olfactory sensory neurons; (2) reduced size of the olfactory bulb; (3) abnormal layer formation in the olfactory bulb; and (4) aberrant rostral migration of the interneuron progenitors. Fez was not expressed in the projection neurons, interneurons or interneuron progenitors. Transgene-mediated expression of Fez in olfactory sensory neurons significantly rescued the abnormalities in olfactory axon projection and in the morphogenesis of the olfactory bulb in Fez-knockout mice. Thus, Fez is cell-autonomously required for the axon termination of olfactory sensory neurons, and Fez non-cell-autonomously controls layer formation and interneuron development in the olfactory bulb. These findings suggest that signals from olfactory sensory neurons contribute to the proper formation of the olfactory bulb.
Fez是一种锌指基因,编码一种转录抑制因子,在妊娠中期的嗅觉上皮、下丘脑、腹外侧皮层和丘脑前核中表达。为了揭示其功能,我们培育了Fez基因缺陷小鼠。Fez基因缺陷小鼠在嗅觉系统中表现出几种异常:(1)嗅觉感觉神经元的轴突投射受损;(2)嗅球体积减小;(3)嗅球中分层异常;(4)中间神经元祖细胞的异常向头侧迁移。Fez在投射神经元、中间神经元或中间神经元祖细胞中不表达。转基因介导的Fez在嗅觉感觉神经元中的表达显著挽救了Fez基因敲除小鼠嗅觉轴突投射和嗅球形态发生的异常。因此,Fez对于嗅觉感觉神经元的轴突终末是细胞自主必需的,并且Fez非细胞自主地控制嗅球中的分层形成和中间神经元发育。这些发现表明来自嗅觉感觉神经元的信号有助于嗅球的正常形成。