Research
| Title： | Transcriptional factors Eaf1/2 inhibit endoderm and mesoderm formation via suppressing TGF-beta signaling |
|---|---|
| First author： | Liu, Jing-Xia; Xu, Qin-Han; Li, Sen; Yu, XueDong; Liu, Wenye; Ouyang, Gang; Zhang, Ting; Chen, Ling-Ling |
| Journal： | BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS |
| Years： | 2017 |
| DOI： | 10.1016/j.bbagrm.2017.09.001 |
| Abstract： | Eaf family genes act in multiple cellular responses such as tumor suppression and embryonic development. In our previous work, Eaf1/2 was found to modulate convergence and extension (C & E) movements and pattern the embryonic anterior-posterior axis during zebrafish embryogenesis. Here, we found that loss-of-function of eaf1/2 caused expanded mesoderm and endoderm in zebrafish embryos and led to the recovery of endoderm specification in TGF-beta factor-mzoep(tz257) mutants, while gain-of-function of eaf1/2 induced reduced mesoderm and endoderm. Analyses of gene expression profiles in Eaf deleted or over-expressed mammalian cells indicated that the roles of Eaf1 and Eaf2 in inhibiting TGF-beta signals were conserved from fish to mammals. By taking advantages of TGF-beta reporters, eaf1/2-fused engrailed proteins, and P53(M214K) mutant, we revealed that Eaf1 and Eaf2 might suppress TGF-beta transduction by synergistically inhibiting none-P53 and P53-required TGF-beta signaling. Furthermore, Eaf1/2 might co-localize and interact with TGF-beta transcriptional factors in the transcriptional complex as repressors to target and suppress TGF-beta signaling activity. Our study unveiled a previously unrecognized link of Eaf1/2 genes with TGF-beta and P53 in vertebrates and demonstrated a conservation of TGF-beta suppression activity for Eaf1/2 family genes from fish to mammals, which might shed some light on the molecular mechanistic basis of Eaf1 and Eaf2 in tumor suppression. |
