Detailed Information on Publication Record
2000
Genetic analysis of the Saccharomyces cerevisiae Sgs1 helicase defines an essential function for the Sgs1-Top3 complex in the absence of SRS2 or TOP1.
DUNO, Morten, Bo THOMSEN, Ole WESTERGAARD, Lumír KREJČÍ, Christian BENDIXEN et. al.Basic information
Original name
Genetic analysis of the Saccharomyces cerevisiae Sgs1 helicase defines an essential function for the Sgs1-Top3 complex in the absence of SRS2 or TOP1.
Name in Czech
Genetic analysis of the Saccharomyces cerevisiae Sgs1 helicase defines an essential function for the Sgs1-Top3 complex in the absence of SRS2 or TOP1.
Authors
DUNO, Morten (208 Denmark), Bo THOMSEN (208 Denmark), Ole WESTERGAARD (208 Denmark), Lumír KREJČÍ (203 Czech Republic, guarantor) and Christian BENDIXEN (208 Denmark)
Edition
Mol Gen Genet, 2000, 1617-4615
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
Genetics and molecular biology
Country of publisher
Denmark
Confidentiality degree
není předmětem státního či obchodního tajemství
Organization unit
Faculty of Science
Keywords in English
Recombination; repair; Sgs1;Top3
Tags
Tags
International impact, Reviewed
Změněno: 15/5/2009 23:04, doc. Mgr. Lumír Krejčí, Ph.D.
V originále
The Saccharomyces cerevisiae gene SGS1 encodes a DNA helicase that shows homology to the Escherichia coli protein RecQ and the products of the BLM and WRN genes in humans, which are defective in Bloom's and Werner's syndrome, respectively. Recently, it has been proposed that this helicase is involved in maintaining the integrity of the rDNA and that loss of Sgs1 function leads to accelerated aging. Sgs1 has been isolated on the basis of its genetic interaction with both topoisomerase I and topoisomerase III, as well as in a two-hybrid screen for proteins that interact with the C-terminal portion of topoisomerase II. We have defined the minimal structural elements of Sgs1 required for its interactions with the three topoisomerases, and demonstrate that the complex phenotypes associated with sgs1 mutants are a consequence of a dysfunctional Sgs1-Top3 complex. We also report that the synthetic relationship between mutations in SGS1 and SRS2, which encodes another helicase implicated in recombinational repair, likewise result from a dysfunctional Sgs1-Top3 interaction. Our findings indicate that Sgs1 may act on different DNA structures depending on the activity of topoisomerase I, Srs2 and topoisomerase III.
In Czech
Genetická charakterizace SGS1 a TOP1 vztahů