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  1. Article ; Online: Unusual DNA duplex and hairpin motifs.

    Chou, Shan-Ho / Chin, Ko-Hsin / Wang, Andrew H-J

    Nucleic acids research

    2003  Volume 31, Issue 10, Page(s) 2461–2474

    Abstract: ... duplex and hairpin motifs in the presence (trans) or absence (cis) of ligands. Several principles ... groove to form a compact loop structure. Identification of such diverse duplex or hairpin motifs greatly ... mismatches can occur in a B-DNA duplex when sheared base pairs are adjacent to each other to confer extensive ...

    Abstract Single-stranded DNA or double-stranded DNA has the potential to adopt a wide variety of unusual duplex and hairpin motifs in the presence (trans) or absence (cis) of ligands. Several principles for the formation of those unusual structures have been established through the observation of a number of recurring structural motifs associated with different sequences. These include: (i) internal loops of consecutive mismatches can occur in a B-DNA duplex when sheared base pairs are adjacent to each other to confer extensive cross- and intra-strand base stacking; (ii) interdigitated (zipper-like) duplex structures form instead when sheared G*A base pairs are separated by one or two pairs of purine*purine mismatches; (iii) stacking is not restricted to base, deoxyribose also exhibits the potential to do so; (iv) canonical G*C or A.T base pairs are flexible enough to exhibit considerable changes from the regular H-bonded conformation. The paired bases become stacked when bracketed by sheared G.A base pairs, or become extruded out and perpendicular to their neighboring bases in the presence of interacting drugs; (v) the purine-rich and pyrimidine-rich loop structures are notably different in nature. The purine-rich loops form compact triloop structures closed by a sheared G*A, A*A, A*C or sheared-like G(anti)*C(syn) base pair that is stacked by a single residue. On the other hand, the pyrimidine-rich loops with a thymidine in the first position exhibit no base pairing but are characterized by the folding of the thymidine residue into the minor groove to form a compact loop structure. Identification of such diverse duplex or hairpin motifs greatly enlarges the repertoire for unusual DNA structural formation.
    MeSH term(s) Base Pair Mismatch/genetics ; Base Pairing/genetics ; Base Sequence ; DNA/chemistry ; DNA/genetics ; Hydrogen Bonding ; Models, Molecular ; Nucleic Acid Conformation ; Nucleic Acid Heteroduplexes/chemistry ; Nucleic Acid Heteroduplexes/genetics
    Chemical Substances Nucleic Acid Heteroduplexes ; DNA (9007-49-2)
    Language English
    Publishing date 2003-03-18
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 186809-3
    ISSN 1362-4962 ; 1362-4954 ; 0301-5610 ; 0305-1048
    ISSN (online) 1362-4962 ; 1362-4954
    ISSN 0301-5610 ; 0305-1048
    DOI 10.1093/nar/gkg367
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: NF-Y controls transcription of the minute virus of mice P4 promoter through interaction with an unusual binding site.

    Gu, Z / Plaza, S / Perros, M / Cziepluch, C / Rommelaere, J / Cornelis, J J

    Journal of virology

    1995  Volume 69, Issue 1, Page(s) 239–246

    Abstract: ... and to the external and internal arms of the extended duplex replication form, respectively ... sequence. USF and NF-Y had distinct but overlapping sequence requirements for binding, suggesting ... that their associations with MVM DNA were mutually exclusive. Because of the palindromic nature of MVM DNA terminal ...

    Abstract Electrophoretic mobility shift assays performed with nuclear extracts from human fibroblasts revealed the formation of two major protein complexes with an oligonucleotide (nucleotides 78 to 107) from the palindromic region located upstream from the minute virus of mice (MVM) P4 promoter. It was shown that this oligonucleotide bound USF at the enhancer E box CACATG. The second complex contained the transcription factor NF-Y, whose association was surprising because its target sequence lacks the canonical CCAAT motif present in all mammalian NF-Y binding sites identified so far. The MVM NF-Y recognition element instead contains the CCAAC sequence. USF and NF-Y had distinct but overlapping sequence requirements for binding, suggesting that their associations with MVM DNA were mutually exclusive. Because of the palindromic nature of MVM DNA terminal sequences, NF-Y associated with the three nucleotide configurations corresponding to the hairpin structure and to the external and internal arms of the extended duplex replication form, respectively. However, owing to the imperfection of the palindrome, the binding of USF was restricted to the internal arm. Point mutations that suppressed the in vitro binding of NF-Y to the internal palindromic arm reduced the activity of the resident P4 promoter, while those preventing complex formation with USF did not, as determined by transient expression assays using the luciferase reporter gene. The data led to the identification of a novel P4 upstream regulatory region capable of interacting with two transcription factors, from which one (NF-Y) appeared to upmodulate the activity of the promoter.
    MeSH term(s) Base Sequence ; Binding Sites ; CCAAT-Enhancer-Binding Proteins ; DNA, Viral/metabolism ; DNA-Binding Proteins/metabolism ; Humans ; Minute Virus of Mice/genetics ; Molecular Sequence Data ; Promoter Regions, Genetic ; Transcription Factors/metabolism ; Transcription, Genetic ; Upstream Stimulatory Factors
    Chemical Substances CCAAT-Enhancer-Binding Proteins ; DNA, Viral ; DNA-Binding Proteins ; Transcription Factors ; USF1 protein, human ; Upstream Stimulatory Factors
    Language English
    Publishing date 1995-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/JVI.69.1.239-246.1995
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: An unusual DNA structure detected in a telomeric sequence under superhelical stress and at low pH.

    Lyamichev, V I / Mirkin, S M / Danilevskaya, O N / Voloshin, O N / Balatskaya, S V / Dobrynin, V N / Filippov, S A / Frank-Kamenetskii, M D

    Nature

    1989  Volume 339, Issue 6226, Page(s) 634–637

    Abstract: ... motifs (n greater than or equal to m) and, in the single-stranded state, form hairpins stabilized by non ... canonical G.G pairs. In the duplex state and under superhelical stress they exhibit hypersensitivity to SI ... a hairpin stabilized by non-Watson-Crick base pairs C.C+ and A.A+, whereas the G-rich strand remains ...

    Abstract Telomeric sequences of DNA, which are found at the ends of linear chromosomes, have been attracting attention as potential sites for the formation of unusual DNA structures. They consist of (GnTm) or (GnATm) motifs (n greater than or equal to m) and, in the single-stranded state, form hairpins stabilized by non-canonical G.G pairs. In the duplex state and under superhelical stress they exhibit hypersensitivity to SI nuclease which by analogy with homopurine-homopyrimidine sequences may reflect the formation of an unusual structure. To determine whether this is the case we have inserted into a plasmid the Tetrahymena telomeric motif (G4T2).(A2C4) and probed it by two-dimensional gel electrophoresis, chemical modification and oligonucleotide binding. Our data demonstrate that, under superhelical stress and at low pH, the insert does indeed adopt a novel DNA conformation. We have concluded that in this structure the C-rich strand forms a hairpin stabilized by non-Watson-Crick base pairs C.C+ and A.A+, whereas the G-rich strand remains unstructured. We term this new DNA structure the (C,A)-hairpin.
    MeSH term(s) DNA ; Electrophoresis, Gel, Two-Dimensional ; Hydrogen-Ion Concentration ; Models, Molecular ; Molecular Structure ; Plasmids
    Chemical Substances DNA (9007-49-2)
    Language English
    Publishing date 1989-06-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/339634a0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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