A combinatorial code for gene expression generated by transcription factor Bach2 and MAZR (MAZ-related factor) through the BTB/POZ domain.
Bach2 is a B-cell- and neuron-specific transcription repressor that forms heterodimers with the Maf-related oncoproteins. We show here that Bach2 activates transcription by interacting with its novel partner MAZR. MAZR was isolated by the yeast two-hybrid screen using the BTB/POZ domain of Bach2 as bait. Besides the BTB/POZ domain, MAZR ... possesses Zn finger motifs that are closely related to those of the Myc-associated Zn finger (MAZ) protein. MAZR mRNA was coexpressed with Bach2 in B cells among hematopoietic cells and in developing mouse limb buds, suggesting a cooperative role for MAZR and Bach2 in these cells. MAZR forms homo- and hetero-oligomers with Bach2 through the BTB domain, which oligomers bind to guanine-rich sequences. Unlike MAZ, MAZR functioned as a strong activator of the c-myc promoter in transfection assays with B cells. However, it does not possess a typical activation domain, suggesting a role for it as an unusual type of transactivator. The fgf4 gene, which regulates morphogenesis of limb buds, contains both guanine-rich sequences and a Bach2 binding site in its regulatory region. In transfection assays using fibroblast cells, the fgf4 gene was upregulated in the presence of both MAZR and Bach2 in a BTB/POZ domain-dependent manner. The results provide a new perspective on the function of BTB/POZ domain factors and indicate that BTB/POZ domain-mediated oligomers of transcription factors may serve as combinatorial codes for gene expression.
Mesh Terms:
Amino Acid Sequence, Animals, Base Sequence, Basic-Leucine Zipper Transcription Factors, Cell Line, DNA-Binding Proteins, Embryonic and Fetal Development, Gene Expression Regulation, Mice, Molecular Sequence Data, Neoplasm Proteins, Repressor Proteins, Sequence Alignment, Sequence Analysis, DNA, Transcription Factors, Transfection
Amino Acid Sequence, Animals, Base Sequence, Basic-Leucine Zipper Transcription Factors, Cell Line, DNA-Binding Proteins, Embryonic and Fetal Development, Gene Expression Regulation, Mice, Molecular Sequence Data, Neoplasm Proteins, Repressor Proteins, Sequence Alignment, Sequence Analysis, DNA, Transcription Factors, Transfection
Mol. Cell. Biol.
Date: Mar. 01, 2000
PubMed ID: 10669750
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