Visualization by BiFC of different C/EBP{beta} dimers and their interaction with HP1{alpha} reveals a differential subnuclear distribution of complexes in living cells
Journal Article
·
· Experimental Cell Research
- Instituto de Biologia y Medicina Experimental, CONICET, Buenos Aires (Argentina)
- Chromosome Biology Group, Imperial College of London, London (United Kingdom)
- Dept. of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI (United States)
- Dept. of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI (United States)
How the co-ordinated events of gene activation and silencing during cellular differentiation are influenced by spatial organization of the cell nucleus is still poorly understood. Little is known about the molecular mechanisms controlling subnuclear distribution of transcription factors, and their interplay with nuclear proteins that shape chromatin structure. Here we show that C/EBP{beta} not only associates with pericentromeric heterochromatin but also interacts with the nucleoskeleton upon induction of adipocyte differentiation of 3T3-L1 cells. Different C/EBP{beta} dimers localize in different nuclear domains. Using BiFC in living cells, we show that LAP (Liver Activating Protein) homodimers localize in euchromatin and heterochromatin. In contrast, LIP (Liver Inhibitory Protein) homodimers localize exclusively in heterochromatin. Importantly, their differential subnuclear distribution mirrors the site for interaction with HP1{alpha}. HP1{alpha} inhibits LAP transcriptional capacity and occupies the promoter of the C/EBP{beta}-dependent gene c/ebp{alpha} in 3T3-L1 preadipocytes. When adipogenesis is induced, HP1{alpha} binding decreases from c/ebp{alpha} promoter, allowing transcription. Thus, the equilibrium among different pools of C/EBP{beta} associated with chromatin or nucleoskeleton, and dynamic changes in their interaction with HP1{alpha}, play key roles in the regulation of C/EBP target genes during adipogenesis.
- OSTI ID:
- 22212103
- Journal Information:
- Experimental Cell Research, Journal Name: Experimental Cell Research Journal Issue: 6 Vol. 317; ISSN 0014-4827; ISSN ECREAL
- Country of Publication:
- United States
- Language:
- English
Similar Records
Crystal Structure of the HP1-EMSY Complex Reveals an Unusual Mode of HP1 Binding
Bisindoylmaleimide I suppresses adipocyte differentiation through stabilization of intracellular {beta}-catenin protein
Artesunate inhibits adipogeneis in 3T3-L1 preadipocytes by reducing the expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3
Journal Article
·
Sat Dec 31 23:00:00 EST 2005
· Structure
·
OSTI ID:914308
Bisindoylmaleimide I suppresses adipocyte differentiation through stabilization of intracellular {beta}-catenin protein
Journal Article
·
Thu Feb 28 23:00:00 EST 2008
· Biochemical and Biophysical Research Communications
·
OSTI ID:21043640
Artesunate inhibits adipogeneis in 3T3-L1 preadipocytes by reducing the expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3
Journal Article
·
Fri May 20 00:00:00 EDT 2016
· Biochemical and Biophysical Research Communications
·
OSTI ID:22598739