MBD3L1 is a transcriptional repressor that interacts with methyl-CpG-binding protein 2 (MBD2) and components of the NuRD complex.
Methyl-CpG-binding domain proteins 2 and 3 (MBD2 and MBD3) are transcriptional repressors that contain methyl-CpG binding domains and are components of a CpG-methylated DNA binding complex named MeCP1. Methyl-CpG-binding protein 3-like 1 (MBD3L1) is a protein with substantial homology to MBD2 and MBD3, but it lacks the methyl-CpG binding domain. ... MBD3L1 interacts with MBD2 and MBD3 in vitro and in yeast two-hybrid assays. Gel shift experiments with a CpG-methylated DNA probe indicate that recombinant MBD3L1 can supershift an MBD2-methylated DNA complex. In vivo, MBD3L1 associates with and colocalizes with MBD2 but not with MBD3 and is recruited to 5-methylcytosine-rich pericentromeric heterochromatin in mouse cells. In glutathione S-transferase pull-down assays MBD3L1 is found associated with several known components of the MeCP1.NuRD complex, including HDAC1, HDAC2, MTA2, MBD2, RbAp46, and RbAp48, but MBD3 is not found in the MBD3L1-bound fraction. MBD3L1 enhances transcriptional repression of methylated DNA by MBD2. The data are consistent with a role of MBD3L1 as a methylation-dependent transcriptional repressor that may interchange with MBD3 as an MBD2-interacting component of the NuRD complex. MBD3L1 knockout mice were created and were found to be viable and fertile, indicating that MBD3L1 may not be essential or there is functional redundancy (through MBD3) in this pathway. Overall, this study reveals additional complexities in the mechanisms of transcriptional repression by the MBD family proteins.
Mesh Terms:
Animals, Base Sequence, Binding Sites, COS Cells, Cell Line, DNA, DNA-Binding Proteins, Hela Cells, Histone Deacetylases, Humans, Mi-2 Nucleosome Remodeling and Deacetylase Complex, Mice, Mice, Knockout, Models, Biological, Multiprotein Complexes, NIH 3T3 Cells, Protein Structure, Tertiary, Recombinant Fusion Proteins, Repressor Proteins
Animals, Base Sequence, Binding Sites, COS Cells, Cell Line, DNA, DNA-Binding Proteins, Hela Cells, Histone Deacetylases, Humans, Mi-2 Nucleosome Remodeling and Deacetylase Complex, Mice, Mice, Knockout, Models, Biological, Multiprotein Complexes, NIH 3T3 Cells, Protein Structure, Tertiary, Recombinant Fusion Proteins, Repressor Proteins
J. Biol. Chem.
Date: Dec. 10, 2004
PubMed ID: 15456747
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