Literature DB >> 3948243

Homologous pairing of DNA molecules by Ustilago rec1 protein is promoted by sequences of Z-DNA.

E B Kmiec, W K Holloman.   

Abstract

Plasmids containing Z-DNA stretches can be paired and linked by combined action of Ustilago rec1 protein and topoisomerase. The product formed is a hemicatenated dimer in which two DNA rings are topologically intertwined at a region of homology. Superhelicity governs the reaction. Formation of linked product is coupled with formation of Z-DNA in the plasmid, a process dependent on the superhelix density. Pairing appears to initiate within the Z-DNA sequence, not at the unwound B-Z junction. The reaction can be blocked by a Z-DNA-specific binding protein, namely Z-DNA antibody. Plasmids with alternating Z-DNA dG-dC sequences at different sites on otherwise homologous molecules can be linked at the dG-dC sequences. However, a plasmid with a (dG-dC)n.(dG-dC)n Z-DNA stretch cannot be linked with a plasmid containing a (dG-dT)n.(dC-dA)n Z-DNA stretch.

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Year:  1986        PMID: 3948243     DOI: 10.1016/0092-8674(86)90264-3

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  40 in total

1.  Hemicatenanes form upon inhibition of DNA replication.

Authors:  I Lucas; O Hyrien
Journal:  Nucleic Acids Res       Date:  2000-05-15       Impact factor: 16.971

2.  Microsatellite evolution: polarity of substitutions within repeats and neutrality of flanking sequences.

Authors:  J Brohede; H Ellegren
Journal:  Proc Biol Sci       Date:  1999-04-22       Impact factor: 5.349

3.  Nonrandom integration of retroviral DNA in vitro: effect of CpG methylation.

Authors:  Y Kitamura; Y M Lee; J M Coffin
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-15       Impact factor: 11.205

4.  Gene transfer system for the phytopathogenic fungus Ustilago maydis.

Authors:  J Wang; D W Holden; S A Leong
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

5.  Interaction of recA protein with left-handed Z-DNA.

Authors:  P Krishna; A R Morgan; J H van de Sande
Journal:  Biochem J       Date:  1991-05-01       Impact factor: 3.857

6.  The ubiquitous potential Z-forming sequence of eucaryotes, (dT-dG)n . (dC-dA)n, is not detectable in the genomes of eubacteria, archaebacteria, or mitochondria.

Authors:  D S Gross; W T Garrard
Journal:  Mol Cell Biol       Date:  1986-08       Impact factor: 4.272

7.  Linkage disequilibrium between two highly polymorphic microsatellites.

Authors:  R Sherrington; G Melmer; M Dixon; D Curtis; B Mankoo; G Kalsi; H Gurling
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

8.  A potential Z-DNA-forming sequence is located between two transcription units alternatively expressed during development of Drosophila hydei.

Authors:  A Jimenez-Ruiz; J M Requena; M C Lopez; C Alonso
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

Review 9.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

Authors:  P Vogt
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

10.  Nonrandom distribution of chloroplast recombination events in Chlamydomonas reinhardtii: evidence for a hotspot and an adjacent cold region.

Authors:  S M Newman; E H Harris; A M Johnson; J E Boynton; N W Gillham
Journal:  Genetics       Date:  1992-10       Impact factor: 4.562

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