Skip Navigation

This Article
Right arrow Print PDF (3461K)
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 arrow Search for citing articles in:
ISI Web of Science (29)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Kohwi-Shigematsu, T.
Right arrow Articles by Kohwi, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kohwi-Shigematsu, T.
Right arrow Articles by Kohwi, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1991, Vol. 19, No. 15 4267-4271
© 1991


MOLECULAR BIOLOGY

Detection of triple-helix related structures adopted by poly(dG)-poly(dC) sequences in supercoiled plasmid DNA

T. Kohwi-Shigematsu and Y. Kohwi

La Jolla Cancer Research Foundation 10901 N.Torrey Pines Rd, La Jolla, CA 92037, USA

Received February 11, 1991. Revised June 19, 1991. Accepted June 19, 1991.

Negative superhelical strain induces the poly(dG) poly(dC) sequence to adopt two totally different types of triple-helices, either a dG.dG.dC triplex in the presence of Mg ++ at both neutral and acidic pHs or a protonated dC + .dG.dC triplex in the absence of Mg ++ ions at acidic pH (1). To examine whether there are still other types of non-B DNA structures formed by the same sequence, we constructed supercoiled plasmid DNAs harboring varying lengths of the poly(dG) tract, and the structures adopted by each supercoiled plasmid DNA were studied with a chemical probe, chloroacetaldehyde. The potential of a poly(dG) poly(dC) sequence to adopt non-B DNA structures depends critically on the length of the tract. Furthermore, in the presence of Mg + + and at a mildly acidic pH, in addition to the expected dG.dG.dC triplex detected for the poly(dG) tracts of 14 to 30 base pairs (bp), new structures were also detected for the tracts longer than 35 bp. The structure formed by a poly(dG) tract of 45 bp revealed chemical reaction patterns consistent with a dG.dG.dC triplex and protonated dC+.dG.dC triple-helices fused together. This structure lacks single-stranded stretches typical of intramolecular triplexes.


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
T. Yamagishi, S. Hirose, and T. Kondo
Secondary DNA structure formation for Hoxb9 promoter and identification of its specific binding protein
Nucleic Acids Res., April 1, 2008; 36(6): 1965 - 1975.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
A. Kotlyar, N. Borovok, T. Molotsky, D. Klinov, B. Dwir, and E. Kapon
Synthesis of novel poly(dG)-poly(dG)-poly(dC) triplex structure by Klenow exo- fragment of DNA polymerase I
Nucleic Acids Res., November 27, 2005; 33(20): 6515 - 6521.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
V. N. Potaman, E. A. Oussatcheva, Y. L. Lyubchenko, L. S. Shlyakhtenko, S. I. Bidichandani, T. Ashizawa, and R. R. Sinden
Length-dependent structure formation in Friedreich ataxia (GAA)n{middle dot}(TTC)n repeats at neutral pH
Nucleic Acids Res., February 20, 2004; 32(3): 1224 - 1231.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
Y Kohwi and Y Panchenko
Transcription-dependent recombination induced by triple-helix formation.
Genes & Dev., September 1, 1993; 7(9): 1766 - 1778.
[Abstract] [PDF]


Home page
Genes Dev.Home page
Y Kohwi and T Kohwi-Shigematsu
Altered gene expression correlates with DNA structure.
Genes & Dev., December 1, 1991; 5(12b): 2547 - 2554.
[Abstract] [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.