Literature DB >> 2647731

Intramolecular DNA triplexes in supercoiled plasmids. II. Effect of base composition and noncentral interruptions on formation and stability.

J C Hanvey1, M Shimizu, R D Wells.   

Abstract

The effects of interruptions in the homopurine bias and the G+C content of the homopurine.homopyrimidine (pur.pyr) sequences on intramolecular triplex formation and stability in supercoiled plasmids were evaluated. In addition, the interconversion of triplex and duplex, after altering the stabilizing factors (low pH or supercoiling), was studied. We conclude: (a) a 42-base pair pur.pyr sequence with three consecutive interruptions does not form a large triplex with three unpaired nucleotides in the stem. Instead, a mixture of two smaller (27- and 28-nucleotide) triplexes forms. (b) A 28-nucleotide sequence with a single interruption forms a triplex with one unpaired nucleotide in the stem. This interruption causes the triplex to be 7 degrees C less thermostable and requires more superhelical energy for formation than the control triplex. (c) As the G+C content of a pur.pyr sequence increases, the thermostability of the triplex increases and the triplex requires less supercoiling for formation. (d) The interconversion between duplex and triplex is fast. After negative supercoiling is removed, all triplex becomes duplex in about 3 min. When the pH is shifted from 8.0 to 5.2, the conversion of duplex to triplex in a negatively supercoiled plasmid is complete in less than 2 min. Hence, these kinetic properties are consistent with important biological roles for triplexes. In summary, the results from both this and the accompanying paper show that a substantial amount of sequence imperfections is tolerated for triplex formation and stability.

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Year:  1989        PMID: 2647731

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

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Authors:  Gautam Prakash; Eric T Kool
Journal:  J Am Chem Soc       Date:  1992-04-01       Impact factor: 15.419

2.  Spectroscopic and calorimetric investigation on the DNA triplex formed by d(CTCTTCTTTCTTTTCTTTCTTCTC) and d(GAGAAGAAAGA) at acidic pH.

Authors:  L E Xodo; G Manzini; F Quadrifoglio
Journal:  Nucleic Acids Res       Date:  1990-06-25       Impact factor: 16.971

3.  Atypical structures of GAA/TTC trinucleotide repeats underlying Friedreich's ataxia: DNA triplexes and RNA/DNA hybrids.

Authors:  Jiahui Zhang; Ashkan Fakharzadeh; Feng Pan; Christopher Roland; Celeste Sagui
Journal:  Nucleic Acids Res       Date:  2020-09-25       Impact factor: 16.971

4.  Mung bean nuclease cleavage pattern at a polypurine.polypyrimidine sequence upstream from the mouse metallothionein-I gene.

Authors:  A Bacolla; F Y Wu
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

5.  Occurrence of potential cruciform and H-DNA forming sequences in genomic DNA.

Authors:  G P Schroth; P S Ho
Journal:  Nucleic Acids Res       Date:  1995-06-11       Impact factor: 16.971

6.  The herpes simplex virus 1 segment inversion site is specifically cleaved by a virus-induced nuclear endonuclease.

Authors:  F Wohlrab; S Chatterjee; R D Wells
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

7.  Dynamics in the isomerization of intramolecular DNA triplexes in supercoiled plasmids.

Authors:  H Shindo; N Matsumoto; M Shimizu
Journal:  Nucleic Acids Res       Date:  1997-12-01       Impact factor: 16.971

Review 8.  Protein binding to simple repetitive sequences depends on DNA secondary structure(s).

Authors:  W Mäueler; G Bassili; C Epplen; H G Keyl; J T Epplen
Journal:  Chromosome Res       Date:  1999       Impact factor: 4.620

9.  Association of poly-purine/poly-pyrimidine sequences with meiotic recombination hot spots.

Authors:  Andrew T M Bagshaw; Joel P W Pitt; Neil J Gemmell
Journal:  BMC Genomics       Date:  2006-07-18       Impact factor: 3.969

  9 in total

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