Back to Search Start Over

Setdb2 restricts dorsal organizer territory and regulates left-right asymmetry through suppressing fgf8 activity.

Authors :
Peng-Fei Xu
Kang-Yong Zhu
Yi Jin
Yi Chen
Xiao-Jian Sun
Min Deng
Sai-Juan Chen
Zhu Chen
Ting Xi Liu
Source :
Proceedings of the National Academy of Sciences of the United States of America. 2/9/2010, Vol. 107 Issue 6, p2521-2526. 6p. 4 Graphs.
Publication Year :
2010

Abstract

Dorsal organizer formation is one of the most critical steps in early embryonic development. Several genes, and signaling pathways that positively regulate the dorsal organizer development have been identified; however, little is known about the factor(s) that negatively regulates the organizer formation. Here, we show that Setdb2, a SET domain-containing protein possessing potential histone H3K9 methyltransferase activity, restricts dorsal organizer development and regulates left-right asymmetry by suppressing fibroblast growth factor 8 (fgf8) expression. Knockdown of Setdb2 results in a massive expansion of dorsal organizer markers floating head (f/h), goosecoid (gsc), and chordin (chd), as well as a significant increase of fgf8, but not fgf4 mRNAs. Consequently, disrupted midline patterning and resultant randomization of left-right asymmetry are observed in Setdb2-deficient embryos. These characteristic changes induced by Setdb2 deficiency can be nearly corrected by either overexpression of a dominant-negative fgf receptor or knockdown of fgf8, suggesting an essential role for Setdb2-Fgf8 signaling in restricting dorsal organizer territory and regulating left-right asymmetry. These results provide unique evidence that a SET domain-containing protein potentially involved in the epigenetic control negatively regulates dorsal organizer formation during early embryonic development. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
107
Issue :
6
Database :
Academic Search Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
48167658