Literature DB >> 12235386

Topoisomerase III is required for accurate DNA replication and chromosome segregation in Schizosaccharomyces pombe.

Misook Oh1, In-Soon Choi, Sang Dai Park.   

Abstract

The deletion of the top3(+) gene leads to defective nuclear division and lethality in Schizosaccharo myces pombe. This lethality is suppressed by concomitant loss of rqh1(+), the RecQ helicase. Despite extensive investigation, topoisomerase III function and its relationship with RecQ helicase remain poorly understood. We generated top3 temperature-sensitive (top3-ts) mutants and found these to be defective in nuclear division and cytokinesis and to be sensitive to DNA-damaging agents. A temperature shift of top3-ts cells to 37 degrees C, or treatment with hydroxyurea at the permissive temperature, caused an increase in 'cut' (cell untimely torn) cells and elevated rates of minichromosome loss. The viability of top3-ts cells was decreased by a temperature shift during S-phase when compared with a similar treatment in other cell cycle stages. Furthermore, the top3-ts mutant was not sensitive to M-phase specific drugs. These results indicate that topoisomerase III may play an important role in DNA metabolism during DNA replication to ensure proper chromosome segregation. Our data are consistent with Top3 acting downstream of Rqh1 to process the toxic DNA structure produced by Rqh1.

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Year:  2002        PMID: 12235386      PMCID: PMC137115          DOI: 10.1093/nar/gkf531

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  24 in total

Review 1.  Defending genome integrity during DNA replication: a proposed role for RecQ family helicases.

Authors:  R K Chakraverty; I D Hickson
Journal:  Bioessays       Date:  1999-04       Impact factor: 4.345

2.  In vitro mutagenesis and plasmid shuffling: from cloned gene to mutant yeast.

Authors:  R S Sikorski; J D Boeke
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

3.  Targeting, disruption, replacement, and allele rescue: integrative DNA transformation in yeast.

Authors:  R Rothstein
Journal:  Methods Enzymol       Date:  1991       Impact factor: 1.600

4.  The top3(+) gene is essential in Schizosaccharomyces pombe and the lethality associated with its loss is caused by Rad12 helicase activity.

Authors:  M Maftahi; C S Han; L D Langston; J C Hope; N Zigouras; G A Freyer
Journal:  Nucleic Acids Res       Date:  1999-12-15       Impact factor: 16.971

5.  Topoisomerase III is essential for accurate nuclear division in Schizosaccharomyces pombe.

Authors:  A Goodwin; S W Wang; T Toda; C Norbury; I D Hickson
Journal:  Nucleic Acids Res       Date:  1999-10-15       Impact factor: 16.971

6.  SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination.

Authors:  K Myung; A Datta; C Chen; R D Kolodner
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

7.  Topoisomerase III acts upstream of Rad53p in the S-phase DNA damage checkpoint.

Authors:  R K Chakraverty; J M Kearsey; T J Oakley; M Grenon; M A de La Torre Ruiz; N F Lowndes; I D Hickson
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

8.  A hyper-recombination mutation in S. cerevisiae identifies a novel eukaryotic topoisomerase.

Authors:  J W Wallis; G Chrebet; G Brodsky; M Rolfe; R Rothstein
Journal:  Cell       Date:  1989-07-28       Impact factor: 41.582

9.  Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome.

Authors:  S Kitao; A Shimamoto; M Goto; R W Miller; W A Smithson; N M Lindor; Y Furuichi
Journal:  Nat Genet       Date:  1999-05       Impact factor: 38.330

10.  Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.

Authors:  K Yamagata; J Kato; A Shimamoto; M Goto; Y Furuichi; H Ikeda
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

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  8 in total

1.  Top3 processes recombination intermediates and modulates checkpoint activity after DNA damage.

Authors:  Hocine W Mankouri; Ian D Hickson
Journal:  Mol Biol Cell       Date:  2006-08-09       Impact factor: 4.138

2.  Resolution of converging replication forks by RecQ and topoisomerase III.

Authors:  Catherine Suski; Kenneth J Marians
Journal:  Mol Cell       Date:  2008-06-20       Impact factor: 17.970

Review 3.  The dissolution of double Holliday junctions.

Authors:  Anna H Bizard; Ian D Hickson
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-07-01       Impact factor: 10.005

4.  The N-terminal region of the Schizosaccharomyces pombe RecQ helicase, Rqh1p, physically interacts with Topoisomerase III and is required for Rqh1p function.

Authors:  Fouzia Ahmad; Elspeth Stewart
Journal:  Mol Genet Genomics       Date:  2005-02-09       Impact factor: 3.291

5.  TOPO3alpha influences antigenic variation by monitoring expression-site-associated VSG switching in Trypanosoma brucei.

Authors:  Hee-Sook Kim; George A M Cross
Journal:  PLoS Pathog       Date:  2010-07-08       Impact factor: 6.823

6.  Defective p53 engagement after the induction of DNA damage in cells deficient in topoisomerase 3beta.

Authors:  Subhasis Mohanty; Terrence Town; Tomohito Yagi; Christina Scheidig; Kelvin Y Kwan; Heather G Allore; Richard A Flavell; Albert C Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-26       Impact factor: 11.205

7.  Identification of a Functional Type IA Topoisomerase, LdTopIIIβ, from Kinetoplastid Parasite Leishmania donovani.

Authors:  Bijoylaxmi Banerjee; Nilkantha Sen; Hemanta K Majumder
Journal:  Enzyme Res       Date:  2011-05-02

8.  DNA topoisomerase III localizes to centromeres and affects centromeric CENP-A levels in fission yeast.

Authors:  Ulrika Norman-Axelsson; Mickaël Durand-Dubief; Punit Prasad; Karl Ekwall
Journal:  PLoS Genet       Date:  2013-03-14       Impact factor: 5.917

  8 in total

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