Citation: "Temporal mapping of CEBPA and
CEBPB binding during liver regeneration reveals dynamic occupancy and specific regulatory codes for homeostatic and cell cycle gene batteries"; Janus Schou Jakobsen et al.; Genome Research, advance online publication, DOI: 10.1101/gr.146399.112
Upregulation of the translation of ATF4 and other target proteins can then lead to increased transcription of stress-related genes (such as Atf3, Asns,
Cebpb, and Trib3), allowing the cell to synthesize the subset of proteins needed to respond to the stress that initiated the response [10-12].
(307) French investigators demonstrated that nodal PTCL-NOS and ALCL could be distinguished at the molecular level (308) and found that BCL6, PTPN12,
CEBPB, and SERPINA1 genes were differentially expressed in ALK+ ALCL, and CCR7, CNTFR, IL-22, and IL-21 in ALK- ALCL.
The MANI approach was implemented on time-series gene expression data obtained from a network of seven genes that belong to an adipogenesis regulatory network [11]: Kruppel Like Factor 4 (KLF4), CCAAT/Enhancer Binding Protein-alpha (CEBPa), CCAAT/Enhancer Binding Protein-beta (
CEBPb), CCAAT/Enhancer Binding Protein-gamma (CEBPg), GLUcose Transporter type 4 (GLUT4), Xanthine Dehydrogenase (XDH), and Peroxisome Proliferator-Activated Receptorgamma (PPARg) (Figure 4(a)).