» Articles » PMID: 8474455

Localization of a Bidirectional DNA Replication Origin in the Native Locus and in Episomally Amplified Murine Adenosine Deaminase Loci

Overview
Journal Mol Cell Biol
Specialty Cell Biology
Date 1993 May 1
PMID 8474455
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Gene amplification is frequently mediated by the initial production of acentric, autonomously replicating extrachromosomal elements. The 4,000 extrachromosomal copies of the mouse adenosine deaminase (ADA) amplicon in B-1/50 cells initiate their replication remarkably synchronously in early S phase and at approximately the same time as the single-copy chromosomal locus from which they were derived. The abundance of ADA sequences and favorable replication timing characteristics in this system led us to determine whether DNA replication initiates in ADA episomes within a preferred region and whether this region is the same as that used at the corresponding chromosomal locus prior to amplification. This study reports the detection and localization of a discrete set of DNA fragments in the ADA amplicon which label soon after release of synchronized B-1/50 cells into S phase. A switch in template strand complementarity of Okazaki fragments, indicative of the initiation of bidirectional DNA replication, was found to lie within the same region. This putative replication origin is located approximately 28.5 kbp upstream of the 5' end of the ADA gene. The same region initiated DNA replication in the single-copy ADA locus of the parental cells. These analyses provide the first evidence that the replication of episomal intermediates involved in gene amplification initiates within a preferred region and that the same region is used to initiate DNA synthesis within the native locus.

Citing Articles

Modern biology of extrachromosomal DNA: A decade-long voyage of discovery.

Yang Q, Xie Y, Qiao K, Lim J, Wu S Cell Res. 2025; 35(1):11-22.

PMID: 39748050 PMC: 11701097. DOI: 10.1038/s41422-024-01054-8.


CYP2D6: novel genomic structures and alleles.

Kramer W, Walker D, OKane D, Mrazek D, Fisher P, Dukek B Pharmacogenet Genomics. 2009; 19(10):813-22.

PMID: 19741566 PMC: 2862371. DOI: 10.1097/FPC.0b013e3283317b95.


Stabilization of stalled DNA replication forks by the BRCA2 breast cancer susceptibility protein.

Lomonosov M, Anand S, Sangrithi M, Davies R, Venkitaraman A Genes Dev. 2003; 17(24):3017-22.

PMID: 14681210 PMC: 305253. DOI: 10.1101/gad.279003.


Replication initiation patterns in the beta-globin loci of totipotent and differentiated murine cells: evidence for multiple initiation regions.

Aladjem M, Rodewald L, Lin C, Bowman S, Cimbora D, Brody L Mol Cell Biol. 2002; 22(2):442-52.

PMID: 11756541 PMC: 139749. DOI: 10.1128/MCB.22.2.442-452.2002.


Selective entrapment of extrachromosomally amplified DNA by nuclear budding and micronucleation during S phase.

Shimizu N, Itoh N, Utiyama H, Wahl G J Cell Biol. 1998; 140(6):1307-20.

PMID: 9508765 PMC: 2132668. DOI: 10.1083/jcb.140.6.1307.


References
1.
Huberman J, Riggs A . On the mechanism of DNA replication in mammalian chromosomes. J Mol Biol. 1968; 32(2):327-41. DOI: 10.1016/0022-2836(68)90013-2. View

2.
Windle B, Wahl G . Molecular dissection of mammalian gene amplification: new mechanistic insights revealed by analyses of very early events. Mutat Res. 1992; 276(3):199-224. DOI: 10.1016/0165-1110(92)90009-x. View

3.
Leu T, Hamlin J . Activation of a mammalian origin of replication by chromosomal rearrangement. Mol Cell Biol. 1992; 12(6):2804-12. PMC: 364475. DOI: 10.1128/mcb.12.6.2804-2812.1992. View

4.
Von Hoff D, McGill J, Forseth B, Davidson K, Bradley T, Van Devanter D . Elimination of extrachromosomally amplified MYC genes from human tumor cells reduces their tumorigenicity. Proc Natl Acad Sci U S A. 1992; 89(17):8165-9. PMC: 49877. DOI: 10.1073/pnas.89.17.8165. View

5.
Nonet G, Wahl G . Introduction of YACs containing a putative mammalian replication origin into mammalian cells can generate structures that replicate autonomously. Somat Cell Mol Genet. 1993; 19(2):171-92. DOI: 10.1007/BF01233532. View