BMP ligands act redundantly to pattern the dorsal telencephalic midline

被引:45
作者
Hébert, JM
Hayhurst, M
Marks, ME
Kulessa, H
Hogan, BLM
McConnell, SK [1 ]
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[2] Vanderbilt Univ, Med Ctr, Dept Cell & Dev Biol, Nashville, TN USA
[3] Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10467 USA
关键词
BMP signaling; Cre/loxP; Foxg1-Cre; neurogenesis; forebrain;
D O I
10.1002/gene.10183
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The embryonic telencephalon is patterned into several areas that give rise to functionally distinct structures in the adult forebrain. Previous studies have shown that BMP4 and BMP2 can induce features characteristic of the telencephalic midline in cultured explants, suggesting that the normal role of BMP4 in the forebrain is to pattern the medial lateral axis of the telencephalon by promoting midline cell fates. To test this hypothesis directly in vivo, the Bmp4 gene was efficiently disrupted in the telencephalon using a CRE/loxP approach. Analysis of Bmp4-deficient telencephalons fails to reveal a defect in patterning, cell proliferation, differentiation, or apoptosis. The absence of a phenotype in the Bmp4-deficient telencephalon along with recent genetic studies establishing a role for a BMP4 receptor, BMPRIA, in telencephalic midline development, demonstrate that loss of Bmp4 function in the telencephalon can be compensated for by at least one other Bmp gene, the identity of which has not yet been determined. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:214 / 219
页数:6
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