This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!
Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Save citation to file

Add to Collections

Name must be less than 100 characters
Unable to load your collection due to an error
Please try again

Add to My Bibliography

Unable to load your delegates due to an error
Please try again

Your saved search

Would you like email updates of new search results?
Saved Search Alert Radio Buttons
()

Create a file for external citation management software

Your RSS Feed

. 1987 Nov 6;51(3):473-81.
doi: 10.1016/0092-8674(87)90643-x.

The in vivo replication origin of the yeast 2 microns plasmid

Affiliations

Affiliation

  • 1 Department of Molecular and Cellular Biology, Roswell Park Memorial Institute, Buffalo, New York 14263.

The in vivo replication origin of the yeast 2 microns plasmid

J A Huberman et al. Cell. .
. 1987 Nov 6;51(3):473-81.
doi: 10.1016/0092-8674(87)90643-x.

Affiliation

  • 1 Department of Molecular and Cellular Biology, Roswell Park Memorial Institute, Buffalo, New York 14263.

Abstract

We have used two-dimensional neutral/alkaline agarose gel electrophoresis to separate the nascent strands of replicating yeast 2 micron plasmid DNA molecules according to extent of replication, away from nonreplicating molecules and parental strands. Analysis of the lengths of nascent strands by sequential hybridization with short probes shows that replication proceeds bidirectionally from a single origin at map position 3700 +/- 100, coincident with the genetically mapped ARS element. The two recombinational isomers of 2 microns plasmid (forms A and B) replicate with equal efficiency. These results suggest that ARS elements may prove to be replication origins for chromosomal DNA.

PubMed Disclaimer

Publication types

LinkOut - more resources

Cite
Morty Proxy This is a proxified and sanitized view of the page, visit original site.