Literature DB >> 12930956

Fission yeast Rhp51 is required for the maintenance of telomere structure in the absence of the Ku heterodimer.

Tatsuya Kibe1, Kazunori Tomita, Akira Matsuura, Daisuke Izawa, Tsutomu Kodaira, Takashi Ushimaru, Masahiro Uritani, Masaru Ueno.   

Abstract

The Schizosaccharomyces pombe Ku70-Ku80 heterodimer is required for telomere length regulation. Lack of pku70+ results in telomere shortening and striking rearrangements of telomere-associated sequences. We found that the rearrangements of telomere-associated sequences in pku80+ mutants are Rhp51 dependent, but not Rad50 dependent. Rhp51 bound to telomere ends when the Ku heterodimer was not present at telomere ends. We also found that the single-stranded G-rich tails increased in S phase in wild-type strains, while deletion of pku70+ increased the single-stranded overhang in both G2 and S phase. Based on these observations, we propose that Rhp51 binds to the G-rich overhang and promotes homologous pairing between two different telomere ends in the absence of Ku heterodimer. Moreover, pku80 rhp51 double mutants showed a significantly reduced telomere hybridization signal. Our results suggest that, although Ku heterodimer sequesters Rhp51 from telomere ends to inhibit homologous recombination activity, Rhp51 plays important roles for the maintenance of telomere ends in the absence of the Ku heterodimer.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12930956      PMCID: PMC212814          DOI: 10.1093/nar/gkg718

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


  81 in total

1.  Double-strand break repair in the absence of RAD51 in yeast: a possible role for break-induced DNA replication.

Authors:  A Malkova; E L Ivanov; J E Haber
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-09       Impact factor: 11.205

2.  Cell cycle-regulated generation of single-stranded G-rich DNA in the absence of telomerase.

Authors:  I Dionne; R J Wellinger
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-26       Impact factor: 11.205

3.  Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro.

Authors:  P Baumann; F E Benson; S C West
Journal:  Cell       Date:  1996-11-15       Impact factor: 41.582

4.  Telomere-led premeiotic chromosome movement in fission yeast.

Authors:  Y Chikashige; D Q Ding; H Funabiki; T Haraguchi; S Mashiko; M Yanagida; Y Hiraoka
Journal:  Science       Date:  1994-04-08       Impact factor: 47.728

5.  Identification of a Saccharomyces cerevisiae Ku80 homologue: roles in DNA double strand break rejoining and in telomeric maintenance.

Authors:  S J Boulton; S P Jackson
Journal:  Nucleic Acids Res       Date:  1996-12-01       Impact factor: 16.971

6.  DNA structure-dependent requirements for yeast RAD genes in gene conversion.

Authors:  N Sugawara; E L Ivanov; J Fishman-Lobell; B L Ray; X Wu; J E Haber
Journal:  Nature       Date:  1995-01-05       Impact factor: 49.962

7.  Cloning the RAD51 homologue of Schizosaccharomyces pombe.

Authors:  D F Muris; K Vreeken; A M Carr; B C Broughton; A R Lehmann; P H Lohman; A Pastink
Journal:  Nucleic Acids Res       Date:  1993-09-25       Impact factor: 16.971

8.  The DNA-binding protein Hdf1p (a putative Ku homologue) is required for maintaining normal telomere length in Saccharomyces cerevisiae.

Authors:  S E Porter; P W Greenwell; K B Ritchie; T D Petes
Journal:  Nucleic Acids Res       Date:  1996-02-15       Impact factor: 16.971

9.  Catalysis of ATP-dependent homologous DNA pairing and strand exchange by yeast RAD51 protein.

Authors:  P Sung
Journal:  Science       Date:  1994-08-26       Impact factor: 47.728

10.  Cloning and characterisation of the Schizosaccharomyces pombe rad32 gene: a gene required for repair of double strand breaks and recombination.

Authors:  M Tavassoli; M Shayeghi; A Nasim; F Z Watts
Journal:  Nucleic Acids Res       Date:  1995-02-11       Impact factor: 16.971

View more
  11 in total

1.  Microhomology-mediated end joining in fission yeast is repressed by pku70 and relies on genes involved in homologous recombination.

Authors:  Anabelle Decottignies
Journal:  Genetics       Date:  2007-05-04       Impact factor: 4.562

2.  Roles of heterochromatin and telomere proteins in regulation of fission yeast telomere recombination and telomerase recruitment.

Authors:  Lyne Khair; Lakxmi Subramanian; Bettina A Moser; Toru M Nakamura
Journal:  J Biol Chem       Date:  2009-12-29       Impact factor: 5.157

3.  Fission yeast Dna2 is required for generation of the telomeric single-strand overhang.

Authors:  Kazunori Tomita; Tatsuya Kibe; Ho-Young Kang; Yeon-Soo Seo; Masahiro Uritani; Takashi Ushimaru; Masaru Ueno
Journal:  Mol Cell Biol       Date:  2004-11       Impact factor: 4.272

4.  A novel allele of fission yeast rad11 that causes defects in DNA repair and telomere length regulation.

Authors:  Yuuki Ono; Kazunori Tomita; Akira Matsuura; Takuro Nakagawa; Hisao Masukata; Masahiro Uritani; Takashi Ushimaru; Masaru Ueno
Journal:  Nucleic Acids Res       Date:  2003-12-15       Impact factor: 16.971

5.  Recombination-based telomere maintenance is dependent on Tel1-MRN and Rap1 and inhibited by telomerase, Taz1, and Ku in fission yeast.

Authors:  Lakxmi Subramanian; Bettina A Moser; Toru M Nakamura
Journal:  Mol Cell Biol       Date:  2007-12-26       Impact factor: 4.272

6.  Fission yeast Taz1 and RPA are synergistically required to prevent rapid telomere loss.

Authors:  Tatsuya Kibe; Yuuki Ono; Koichiro Sato; Masaru Ueno
Journal:  Mol Biol Cell       Date:  2007-04-11       Impact factor: 4.138

7.  Nucleostemin prevents telomere damage by promoting PML-IV recruitment to SUMOylated TRF1.

Authors:  Joseph K Hsu; Tao Lin; Robert Y L Tsai
Journal:  J Cell Biol       Date:  2012-05-28       Impact factor: 10.539

8.  Ku stabilizes replication forks in the absence of Brc1.

Authors:  Arancha Sánchez; Paul Russell
Journal:  PLoS One       Date:  2015-05-12       Impact factor: 3.240

9.  Extending the Schizosaccharomyces pombe molecular genetic toolbox.

Authors:  Dorota Fennessy; Agnes Grallert; Andrea Krapp; Adisa Cokoja; Alan J Bridge; Janni Petersen; Avinash Patel; Victor A Tallada; Elvan Boke; Ben Hodgson; Viesturs Simanis; Iain M Hagan
Journal:  PLoS One       Date:  2014-05-21       Impact factor: 3.240

10.  Acentric chromosome ends are prone to fusion with functional chromosome ends through a homology-directed rearrangement.

Authors:  Yuko Ohno; Yuki Ogiyama; Yoshino Kubota; Takuya Kubo; Kojiro Ishii
Journal:  Nucleic Acids Res       Date:  2015-10-03       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.