TY - JOUR
T1 - Stabilization of ATF4 protein is required for the regulation of epithelial-mesenchymal transition of the avian neural crest
AU - Suzuki, Takashi
AU - Osumi, Noriko
AU - Wakamatsu, Yoshio
N1 - Funding Information:
We thank Dr. Don Newgreen for comments on the manuscript. We are grateful to Dr. Daisuke Sakai for discussions. We thank Drs. C. Erickson, F. Gage, H. Nakamura, M. Uchikawa, S. Nakagawa, and M. Furuse for plasmids and an antibody. This work was supported in part by a grant to TS from Japan Science and Technology Agency ( 19. 55041 ).
PY - 2010/8
Y1 - 2010/8
N2 - Epithelial-mesenchymal transition (EMT) permits neural crest cells to delaminate from the epithelial ectoderm and to migrate extensively in the embryonic environment. In this study, we have identified ATF4, a basic-leucine-zipper transcription factor, as one of the neural crest EMT regulators. Although ATF4 alone was not sufficient to drive the formation of migratory neural crest cells, ATF4 cooperated with Sox9 to induce neural crest EMT by controlling the expression of cell-cell and cell-extracellular matrix adhesion molecules. This was likely, at least in part, by inducing the expression of Foxd3, which encodes another neural crest transcription factor. We also found that the ATF4 protein level was strictly regulated by proteasomal degradation and p300-mediated stabilization, allowing ATF4 protein to accumulate in the nuclei of neural crest cells undergoing EMT. Thus, our results emphasize the importance of the regulation of protein stability in the neural crest EMT.
AB - Epithelial-mesenchymal transition (EMT) permits neural crest cells to delaminate from the epithelial ectoderm and to migrate extensively in the embryonic environment. In this study, we have identified ATF4, a basic-leucine-zipper transcription factor, as one of the neural crest EMT regulators. Although ATF4 alone was not sufficient to drive the formation of migratory neural crest cells, ATF4 cooperated with Sox9 to induce neural crest EMT by controlling the expression of cell-cell and cell-extracellular matrix adhesion molecules. This was likely, at least in part, by inducing the expression of Foxd3, which encodes another neural crest transcription factor. We also found that the ATF4 protein level was strictly regulated by proteasomal degradation and p300-mediated stabilization, allowing ATF4 protein to accumulate in the nuclei of neural crest cells undergoing EMT. Thus, our results emphasize the importance of the regulation of protein stability in the neural crest EMT.
KW - ATF4
KW - EMT
KW - Foxd3
KW - Neural crest
KW - P300
KW - Sox9
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U2 - 10.1016/j.ydbio.2010.05.492
DO - 10.1016/j.ydbio.2010.05.492
M3 - Article
C2 - 20580702
AN - SCOPUS:77955269643
SN - 0012-1606
VL - 344
SP - 658
EP - 668
JO - Developmental Biology
JF - Developmental Biology
IS - 2
ER -