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PMID: 2978868 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning of the p53-dependent origin of cellular DNA replication.

Oncogene ·Vol. 3 ·No. 5 ·1988-11-00 ·Pages 509-15

Iguchi-Ariga SM, Okazaki T, Itani T, Ariga H

Abstract

We have recently reported that the c-myc protein may promote cellular DNA replication by binding to the origin of DNA replication (ori) and that an origin of human DNA replication which can autonomously replicate in human cells was cloned as a binding sequence of c-myc protein (Iguchi-Ariga et al., 1987). Here we report that cellular tumor antigen p53 may also participate in cellular DNA replication and another origin of DNA replication was cloned as a possible p53-binding sequence. The sequence could autonomously replicate in Raji cells which express p53 at a high level but not in HL-60 cells in which the coding gene for p53 is largely deleted. Little homology of the sequences was found between c-myc protein-binding ori and p53-binding ori. This suggests that c-myc protein and p53 may independently recognize different ori in chromosomal DNA.

MeSH Terms
Animals Antibodies, Monoclonal Base Sequence Cell Line Cloning, Molecular DNA Replication DNA, Neoplasm/genetics Humans Kinetics Molecular Sequence Data Nuclear Proteins/metabolism Nucleic Acid Conformation Oncogene Proteins/metabolism Oncogenes Phosphoproteins/metabolism Plasmids Restriction Mapping Transfection Tumor Suppressor Protein p53
Chemicals
Antibodies, Monoclonal DNA, Neoplasm Nuclear Proteins Oncogene Proteins Phosphoproteins Tumor Suppressor Protein p53
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Iguchi-Ariga S M
Institute of Medical Science, University of Tokyo, Japan.
Okazaki T
Itani T
Ariga H
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1988-11-00
Pages
509-15
Language
English
Region
England
NLM ID
8711562
Subset
IM
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