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PMID: 2216716 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloned origin of DNA replication in c-myc gene can function and be transmitted in transgenic mice in an episomal state.

Nucleic acids research ·Vol. 18 ·No. 18 ·1990-09-25 ·Pages 5425-32

Sudo K, Ogata M, Sato Y, Iguchi-Ariga SM, Ariga H

Abstract

The c-myc protein has recently been shown to interact with a region possessing putative origin of DNA replication and enhancer activities located 2 kb upstream of the c-myc gene itself. Transgenic mice were obtained by injecting constructs containing this region, termed pmyc(H-P), into fertilized mouse eggs. The transgenic elements were capable of efficient replication in all mouse tissues examined and were maintained in an episomal state even in highly differentiated cells. Moreover, pmyc(H-P) was transmittable to the progeny throughout several generations, which suggests that the fragment derived from the region upstream of the c-myc gene possesses sequences necessary for partition, stability and DNA replication of the plasmid in the cells. In addition, we have shown that the plasmid might be captured only by eggs, not by sperm.

MeSH Terms
Animals Cloning, Molecular DNA Replication Female Genes, myc Humans Male Mice Mice, Transgenic Ovum Pedigree Plasmids Restriction Mapping Spermatozoa
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sudo K
Institute of Medical Science, University of Tokyo, Japan.
Ogata M
Sato Y
Iguchi-Ariga S M
Ariga H
References (15)
15 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1990-09-25
Pages
5425-32
Language
English
Region
England
NLM ID
0411011
PMCID
PMC332220
Subset
IM
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