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(Received for publication, September 11, 1995; and in revised form, December 4, 1995)
DREF, a transcription regulatory factor which specifically binds
to the promoter-activating element DRE (DNA replication-related
element) of DNA replication-related genes, was purified to homogeneity
from nuclear extracts of Drosophila Kc cells. cDNA for DREF
was isolated with the reverse-transcriptase polymerase chain reaction
method using primers synthesized on the basis of partial amino acid
sequences and following screening of cDNA libraries. Deduced from the
nucleotide sequences of cDNA, DREF is a polypeptide of 701 amino acid
residues with a molecular weight of 80,096, which contains three
characteristic regions, rich in basic amino acids, proline, and acidic
amino acids, respectively. Deletion analysis of bacterially expressed
DREF fused with glutathione S-transferase (GST-DREF) indicated
that a part of the N-terminal basic amino acid region (16-115
amino acids) is responsible for the specific binding to DRE. A
polyclonal and four monoclonal antibodies were raised against the
GST-DREF fusion protein. The antibodies inhibited specifically the
transcription of DNA polymerase
promoter in vitro.
Cotransfection experiments using Kc cells demonstrated that
overproduction of DREF protein overcomes the repression of the
proliferating cell nuclear antigen gene promoter by the zerknüllt gene product. These results confirmed
that DREF is a trans-activating factor for DNA replication-related
genes. Immunocytochemical analysis demonstrated the presence of DREF
polypeptide in nuclei after the eighth nuclear division cycle,
suggesting that nuclear accumulation of DREF is important for the
coordinate zygotic expression of DNA replication-related genes carrying
DRE sequences.
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