The promoter of the rat aldolase B (AldB) gene functions in vivo as an origin of DNA replication in the cells in which transcription of the gene is repressed. Previously, we identified two closely related DNA-binding proteins, AIF-C1 and AIF-C2, which repressed the AldB gene promoter. We also reported that the binding site of these proteins, site C, is one of the required DNA elements of the AldB gene origin/promoter for autonomously replicating activity in transfected cells. In the present study, we show that AIF-C1 and AIF-C2 bind directly to Orc1, a subunit of the origin recognition complex (ORC). Deletion analyses revealed a functional domain in AIF-C2 for binding to Orc1, which is located separately from the DNA-binding domain. In addition, we found a novel protein-interacting domain in Orc1 required for the binding of AIF-C2, which was conserved in human, mouse and Chinese hamster, but not in Drosophila, frog and yeast. Thus, it is assumed that in mammalian cells, sequence-specific DNA-binding proteins are involved in recruiting ORC to regulate replication initiation and/or transcription repression.
CITATION STYLE
Saitoh, Y., Miyagi, S., Ariga, H., & Tsutsumi, K. I. (2002, December 1). Functional domains involved in the interaction between Orc1 and transcriptional repressor AIF-C that bind to an origin/promoter of the rat aldolase B gene. Nucleic Acids Research. https://doi.org/10.1093/nar/gkf642
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