Literature DB >> 8321213

Origin activation and formation of single-strand TG1-3 tails occur sequentially in late S phase on a yeast linear plasmid.

R J Wellinger1, A J Wolf, V A Zakian.   

Abstract

In order to understand the mechanisms leading to the complete duplication of linear eukaryotic chromosomes, the temporal order of the events involved in replication of a 7.5-kb Saccharomyces cerevisiae linear plasmid called YLpFAT10 was determined. Two-dimensional agarose gel electrophoresis was used to map the position of the replication origin and the direction of replication fork movement through the plasmid. Replication began near the center of YLpFAT10 at the site in the 2 microns sequences that corresponds to the 2 microns origin of DNA replication. Replication forks proceeded bidirectionally from the origin to the ends of YLpFAT10. Thus, yeast telomeres do not themselves act as origins of DNA replication. The time of origin utilization on YLpFAT10 and on circular 2 microns DNA in the same cells was determined both by two-dimensional gel electrophoresis and by density transfer experiments. As expected, 2 microns DNA replicated in early S phase. However, replication of YLpFAT10 occurred in late S phase. Thus, the time of activation of the 2 microns origin depended upon its physical context. Density transfer experiments established that the acquisition of telomeric TG1-3 single-strand tails, a predicted intermediate in telomere replication, occurred immediately after the replication forks approached the ends of YLpFAT10. Thus, telomere replication may be the very last step in S phase.

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Year:  1993        PMID: 8321213      PMCID: PMC359955          DOI: 10.1128/mcb.13.7.4057-4065.1993

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  44 in total

1.  Telomeric position effect in yeast.

Authors:  L L Sandell; V A Zakian
Journal:  Trends Cell Biol       Date:  1992-01       Impact factor: 20.808

Review 2.  A question of time: replication origins of eukaryotic chromosomes.

Authors:  W L Fangman; B J Brewer
Journal:  Cell       Date:  1992-10-30       Impact factor: 41.582

3.  Effects of excess centromeres and excess telomeres on chromosome loss rates.

Authors:  K W Runge; R J Wellinger; V A Zakian
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

Review 4.  Activation of replication origins within yeast chromosomes.

Authors:  W L Fangman; B J Brewer
Journal:  Annu Rev Cell Biol       Date:  1991

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Authors:  J D Watson
Journal:  Nat New Biol       Date:  1972-10-18

6.  ARS replication during the yeast S phase.

Authors:  W L Fangman; R H Hice; E Chlebowicz-Sledziewska
Journal:  Cell       Date:  1983-03       Impact factor: 41.582

7.  Time of replication of yeast centromeres and telomeres.

Authors:  R M McCarroll; W L Fangman
Journal:  Cell       Date:  1988-08-12       Impact factor: 41.582

8.  Telomere length constancy during aging of Saccharomyces cerevisiae.

Authors:  N P D'Mello; S M Jazwinski
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

9.  DNA sequences of telomeres maintained in yeast.

Authors:  J Shampay; J W Szostak; E H Blackburn
Journal:  Nature       Date:  1984 Jul 12-18       Impact factor: 49.962

10.  Introduction of extra telomeric DNA sequences into Saccharomyces cerevisiae results in telomere elongation.

Authors:  K W Runge; V A Zakian
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

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  47 in total

1.  The function of DNA polymerase alpha at telomeric G tails is important for telomere homeostasis.

Authors:  A Adams Martin; I Dionne; R J Wellinger; C Holm
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

2.  Inactivation of 14-3-3sigma influences telomere behavior and ionizing radiation-induced chromosomal instability.

Authors:  S Dhar; J A Squire; M P Hande; R J Wellinger; T K Pandita
Journal:  Mol Cell Biol       Date:  2000-10       Impact factor: 4.272

3.  Telomere folding is required for the stable maintenance of telomere position effects in yeast.

Authors:  D de Bruin; S M Kantrow; R A Liberatore; V A Zakian
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

4.  MEC3, MEC1, and DDC2 are essential components of a telomere checkpoint pathway required for cell cycle arrest during senescence in Saccharomyces cerevisiae.

Authors:  Shinichiro Enomoto; Lynn Glowczewski; Judith Berman
Journal:  Mol Biol Cell       Date:  2002-08       Impact factor: 4.138

5.  Differential processing of leading- and lagging-strand ends at Saccharomyces cerevisiae telomeres revealed by the absence of Rad27p nuclease.

Authors:  Julie Parenteau; Raymund J Wellinger
Journal:  Genetics       Date:  2002-12       Impact factor: 4.562

6.  Asynchronous replication timing of telomeres at opposite arms of mammalian chromosomes.

Authors:  Ying Zou; Sergei M Gryaznov; Jerry W Shay; Woodring E Wright; Michael N Cornforth
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-20       Impact factor: 11.205

7.  Telomere-bound TRF1 and TRF2 stall the replication fork at telomeric repeats.

Authors:  Rieko Ohki; Fuyuki Ishikawa
Journal:  Nucleic Acids Res       Date:  2004-03-08       Impact factor: 16.971

8.  Telomere capping in non-dividing yeast cells requires Yku and Rap1.

Authors:  Momchil D Vodenicharov; Nancy Laterreur; Raymund J Wellinger
Journal:  EMBO J       Date:  2010-07-13       Impact factor: 11.598

9.  The terminal DNA structure of mammalian chromosomes.

Authors:  R McElligott; R J Wellinger
Journal:  EMBO J       Date:  1997-06-16       Impact factor: 11.598

10.  Tying up the Ends: Plasticity in the Recognition of Single-Stranded DNA at Telomeres.

Authors:  Neil R Lloyd; Thayne H Dickey; Robert A Hom; Deborah S Wuttke
Journal:  Biochemistry       Date:  2016-09-15       Impact factor: 3.162

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