Defective limbic system in mice lacking the tailless gene

被引:151
|
作者
Monaghan, AP
Bock, D
Gass, P
Schwager, A
Wolfer, DP
Lipp, HP
Schutz, G
机构
[1] GERMAN CANC RES CTR,DIV MOL BIOL CELL 1,D-69120 HEIDELBERG,GERMANY
[2] UNIV ZURICH IRCHEL,INST ANAT,CH-8057 ZURICH,SWITZERLAND
关键词
D O I
10.1038/37364
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The gene tailless is a member of the superfamily of genes that encode transcription factors of the ligand-activated nuclear receptor type, and is expressed in the invertebrate and vertebrate brain(1-4). In mice, its transcripts are restricted to the periventricular zone of the forebrain(4), the site of origin of neurons and glia. Here we use homologous recombination to generate mice that lack a functional tailless protein. Homozygous mutant mice are viable at birth, indicating that tailless is not required for prenatal survival; however, adult mutant mice show a reduction in the size of rhinencephalic and limbic structures, including the olfactory, infrarhinal and entorhinal cortex, amygdala and dentate gyrus. Both male and female mice are more aggressive than usual and females lack normal maternal instincts. These animals therefore enable a molecular approach to be taken towards understanding the genetic architecture and morphogenesis of the forebrain.
引用
收藏
页码:515 / 517
页数:3
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