Fra-1 replaces c-Fos-dependent functions in mice

被引:127
作者
Fleischmann, A
Hafezi, F
Elliott, C
Remé, CE
Rüther, U
Wagner, EF [1 ]
机构
[1] IMP, Res Inst Mol Pathol, A-1030 Vienna, Austria
[2] Univ Clin Zurich, Dept Ophthalmol, CH-8091 Zurich, Switzerland
[3] Univ Dusseldorf, Entwicklungs & Mol Biol Tiere, D-40225 Dusseldorf, Germany
关键词
AP-1; c-Fos; Fra-1; knock-in; mouse development;
D O I
10.1101/gad.187900
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Structure-function analysis as well as studies with knock-out and transgenic mice have assigned distinct functions to c-Fos and Fra-1, two components of the transcription factor AP-1 (activator protein-1). To test whether Fra-1 could substitute for c-Fos, we generated knock-in mice that express Fra-1 in place of c-Fos. Fra-1 rescues c-Fos-dependent functions such as bone development and light-induced photoreceptor apoptosis. Importantly, rescue, of bone cell differentiation, but not photoreceptor apoptosis, is gene-dosage dependent. Moreover, Fra-1 fails to substitute for c-Fos in inducing expression of target genes in fibroblasts. These results show that c-Fos and Pra-l have maintained functional equivalence during vertebrate evolution.
引用
收藏
页码:2695 / 2700
页数:6
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