Skip Navigation

This Article
Right arrow Print PDF (703K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Wanka, F.
Right arrow Articles by Eygensteyn, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wanka, F.
Right arrow Articles by Eygensteyn, J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1977, Vol. 4, No. 6 2083-2098
© 1977


Articles

The origin of nascent single-stranded DNA extracted from mammalian cells

Friedrich Wanka, Rob M.G.M.E. Brouns, Jan M.A. Aelen and Jelle Eygensteyn

Department of Chemical Cytology, University of Nijmegen Nijmegen, The Netherlands

Received April 14, 1977. In vitro cultured bovine liver cells were labelled with radioactive thymidine and dissolved in 0.5% sodium dodecyl sulphate. Centrifugation of the lysate through sucrose gradients in a zonal rotor revealed a slowly sedimen-ting fraction of preferentially pulse labelled DNA. The DNA of this zone was further analysed by chromatography on hydroxy-apatite, banding in CaCl density gradients, and sedimentation in neutral and alkaline sucrose gradients. It contained, besides small amounts of fragmented bulk DNA., single-stranded nascent DNA and single-stranded pre-labelled DNA which could be separated from each other by using BrdU as a density label. The density labelling also revealed small amounts of nascent-nascent DNA duplexes. The slowly sedimenting fraction was practically absent from cell lysates which were prepared in 2 M NaCl - 50 µg/ml pronase. The results suggest that nascent single-strands and nascent-nascent duplexes are released from the forks of replicating UNA by branch migration. Pre-labelled single strands may be released by the same mechanism, but the in vivo structure from which they originate has yet to be elucidated.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
C. Booth, E. Griffith, G. Brady, and D. Lydall
Quantitative amplification of single-stranded DNA (QAOS) demonstrates that cdc13-1 mutants generate ssDNA in a telomere to centromere direction
Nucleic Acids Res., November 1, 2001; 29(21): 4414 - 4422.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. M. Cox
Historical overview: Searching for replication help in all of the rec places
PNAS, July 17, 2001; 98(15): 8173 - 8180.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. Postow, C. Ullsperger, R. W. Keller, C. Bustamante, A. V. Vologodskii, and N. R. Cozzarelli
Positive Torsional Strain Causes the Formation of a Four-way Junction at Replication Forks
J. Biol. Chem., January 19, 2001; 276(4): 2790 - 2796.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.