Zinc finger gene fez-like functions in the formation of subplate neurons and thalamocortical axons

被引:96
作者
Hirata, T
Suda, Y
Nakao, K
Narimatsu, M
Hirano, T
Hibi, M
机构
[1] RIKEN, Lab Vertebrate Axis Format, Ctr Dev Biol, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Osaka Univ, Dept Mol Oncol, Grad Sch Med, Suita, Osaka, Japan
[3] Ctr Dev Biol, Lab Anim Resources & Genet Engn, Kobe, Hyogo, Japan
[4] RIKEN, Vertebrate Body Plan Grp, Ctr Dev Biol, Kobe, Hyogo, Japan
关键词
fez-like; mouse; forebrain; thalamocortical tract; subplate; hyperactive behavior;
D O I
10.1002/dvdy.20068
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
fez-like (fezl) is a forebrain-expressed zinc finger gene required for the formation of the hypothalamic dopaminergic and serotonergic (monoaminergic) neurons in zebrafish. To reveal its function in mammals, we analyzed the expression of the mouse orthologue of fezl and generated fezl-deficient mice by homologous recombination. Mouse fezl was expressed specifically in the forebrain from embryonic day 8.5. At mid-gestation, fezi expression was detected in subdomains of the forebrain, including the dorsal telencephalon and ventral diencephalon. Unlike the zebrafish fezl mutant too few, the fezl-deficient mice displayed normal development of hypothalamic monoaminergic neurons, but showed abnormal "hyperactive" behavior. In fezl(-/-) mice, the thalamocortical axons (TCA) were reduced in number and aberrantly projected to the cortex. These mutants had a reduced number of subplate neurons, which are involved in guiding the TCA from the dorsal thalamus, although the subplate neurons were born normally. These results suggest that fezl is required for differentiation or survival of the subiplate neurons, and reduction of the subplate neurons in fezl-deficient mice leads to abnormal development of the TCA, providing a possible link between the transcriptional regulation of forebrain development and hyperactive behavior. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:546 / 556
页数:11
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