The forkhead genes, Foxc1 and Foxc2, regulate paraxial versus intermediate mesoderm cell fate

被引:87
作者
Wilm, B
James, RG
Schultheiss, TA
Hogan, BLM
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] Vanderbilt Univ, Dept Cell Biol, Nashville, TN 37232 USA
[3] Beth Israel Deaconess Med Ctr, Mol Med Unit, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Boston, MA 02215 USA
[5] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
关键词
forkhead genes; paraxial mesoderm; intermediate mesoderm; fate commitment; mouse embryo; chick embryo;
D O I
10.1016/j.ydbio.2004.03.034
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During vertebrate embryogenesis, the newly formed mesoderm is allocated to the paraxial, intermediate, and lateral domains, each giving rise to different cell and tissue types. Here, we provide evidence that the forkhead genes, Foxc1 and Foxc2, play a role in the specification of mesoderm to paraxial versus intermediate fates. Mouse embryos lacking both Foxc1 and Foxc2 show expansion of intermediate mesoderm markers into the paraxial domain, lateralization of somite patterning, and ectopic and disorganized mesonephric tubules. In gain of function studies in the chick embryo, Foxc1 and Foxc2 negatively regulate intermediate mesoderm formation. By contrast, their misexpression in the prospective intermediate mesoderm appears to drive cells to acquire paraxial fate, as revealed by expression of the somite markers Pax7 and Paraxis. Taken together, the data indicate that Foxc1 and Foxc2 regulate the establishment of paraxial versus intermediate mesoderm cell fates in the vertebrate embryo. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 189
页数:14
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