Substrate-specific inhibition of RecQ helicase

Nucleic Acids Research

Volumn 29, Issue 8, 2001, Pages 1765-1771

  Wu, Xiang ^a   Maizels, Nancy ^a,b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CATION; DOUBLE STRANDED DNA; HELICASE; PORPHYRIN DERIVATIVE;

ARTICLE; ASSAY; CONTROLLED STUDY; DNA DENATURATION; ENZYME INHIBITION; ENZYME SPECIFICITY; ENZYME SUBSTRATE; ESCHERICHIA COLI; NONHUMAN; PRIORITY JOURNAL;

ESCHERICHIA COLI; EUKARYOTA; PROKARYOTA;

EID: 0035870569     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/29.8.1765     Document Type: Article

References (32)

1. Escherichia coli RecQ protein is a DNA helicase
2. The yeast type I topoisomerase Top3 interacts with Sgsl, a DNA helicase homolog: A potential eukaryotic reverse gyrase
3. Rqhl +, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest
4. The Bloom's syndrome gene product is homologous to RecQ helicases
5. The Werner syndrome protein is a DNA helicase
6. Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ
7. Cloning of two new human helicase genes of the RecQ family: Biological significance of multiple species in higher eukaryotes
8. Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder
9. Chromosome breakage and rejoining of sister chromatids in Bloom's syndrome
10. Werner syndrome: Entering the helicase era
11. Mutator phenotype of Werner syndrome is characterized by extensive deletions
12. Rothmund-Thomson syndrome
13. Sgs1: A eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation
14. Extrachromosomal rDNA circles-a cause of aging in yeast
15. Accelerated aging and nucleolar fragmentation in yeast sgs1 mutants
16. Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: Implication for genomic instability in human diseases
17. Helix formation by guanylic acid
18. Formation of parallel four-stranded complexes by guanine-rich motifs in DNA and its implications for meiosis
19. A sodium-potassium switch in the formation of four-stranded G4-DNA
20. The Saccharomyces cerevisiae Sgs1 helicase efficiently unwinds G-G paired DNAs
21. The Bloom's syndrome helicase unwinds G4 DNA
22. Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n
23. RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination
24. Porphyrins can catalyze the interconversion of DNA quadruplex structural type
25. 4
26. Fluorescent dyes specific for quadruplex DNA nucleic acids research
27. Sequence and structural selectivity of nucleic acid binding ligands
28. Interactions of TMPyP4 and TMPyP2 with quadruplex DNA. Structural basis for the differential effects on telomerase inhibition
29. Properties of protoporphyrin apomyoglobin complexes and related compounds
30. Potent inhibition of Werner and Bloom helicases by DNA minor groove binding drugs
31. The DNA helicase activities of Rad3 protein of Saccharomyces cerevisiae and helicase II of Escherichia coli are differentially inhibited by covalent and noncovalent DNA modifications