|  Help  |  About  |  Contact Us

Publication : Inhibition of excess nodal signaling during mouse gastrulation by the transcriptional corepressor DRAP1.

First Author  Iratni R Year  2002
Journal  Science Volume  298
Issue  5600 Pages  1996-9
PubMed ID  12471260 Mgi Jnum  J:80667
Mgi Id  MGI:2446759 Doi  10.1126/science.1073405
Citation  Iratni R, et al. (2002) Inhibition of excess nodal signaling during mouse gastrulation by the transcriptional corepressor DRAP1. Science 298(5600):1996-9
abstractText  The formation and patterning of mesoderm during mammalian gastrulation require the activity of Nodal, a secreted mesoderm-inducing factor of the transforming growth factor-beta (TGF-beta) family. Here we show that the transcriptional corepressor DRAP1 has a very specific role in regulation of Nodal activity during mouse embryogenesis. We find that loss of Drap1 leads to severe gastrulation defects that are consistent with increased expression of Nodal and can be partially suppressed by Nodal heterozygosity. Biochemical studies indicate that DRAP1 interacts with and inhibits DNA binding by the winged-helix transcription factor FoxH1 (FAST), a critical component of a positive feedback loop for Nodal activity. We propose that DRAP1 limits the spread of a morphogenetic signal by down-modulating the response to the Nodal autoregulatory loop.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

26 Bio Entities

0 Expression