Literature DB >> 7988285

TEL+CEN antagonism on plasmids involves telomere repeat sequences tracts and gene products that interact with chromosomal telomeres.

S Enomoto1, M S Longtine, J Berman.   

Abstract

In Saccharomyces cerevisiae, circular plasmids that include either a centromere (CEN-plasmids) or a telomere sequence (TEL-plasmids) segregate more efficiently than circular ARS-plasmids. In contrast, circular plasmids that include both telomere and centromere sequences were unstable, a property we term TEL+CEN antagonism. TEL+CEN antagonism required a telomere repeat tract longer than 49 bp although the distance and relative orientation of the centromere and telomere sequences was not critical. TEL+CEN antagonism was alleviated in strains carrying different rap1 alleles including rap1ts, rap1s, and rap1t alleles. Mutations SIR2, SIR3, SIR4, NAT1 and ARD1, genes that influence transcriptional silencing at telomeres and at the silent mating type loci, abolished TEL+CEN antagonism Mutation of SIR1 also partially alleviated TEL-CEN antagonism. In some sir mutant strains short yeast artificial chromosomes (YACs), which are normally unstable, became more stable, suggesting that the same mechanism that caused TEL+CEN antagonism on circular plasmids may contribute to the instability of short linear plasmids.

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Year:  1994        PMID: 7988285     DOI: 10.1007/BF00352248

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  91 in total

1.  Transcriptional silencing and lamins.

Authors:  J F Diffley; B Stillman
Journal:  Nature       Date:  1989-11-02       Impact factor: 49.962

2.  Purification and cloning of a DNA binding protein from yeast that binds to both silencer and activator elements.

Authors:  D Shore; K Nasmyth
Journal:  Cell       Date:  1987-12-04       Impact factor: 41.582

3.  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

4.  The SIR1 gene of Saccharomyces cerevisiae and its role as an extragenic suppressor of several mating-defective mutants.

Authors:  E M Stone; M J Swanson; A M Romeo; J B Hicks; R Sternglanz
Journal:  Mol Cell Biol       Date:  1991-04       Impact factor: 4.272

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

Authors:  R J Wellinger; A J Wolf; V A Zakian
Journal:  Mol Cell Biol       Date:  1993-07       Impact factor: 4.272

6.  A synthetic silencer mediates SIR-dependent functions in Saccharomyces cerevisiae.

Authors:  F J McNally; J Rine
Journal:  Mol Cell Biol       Date:  1991-11       Impact factor: 4.272

7.  Silent domains are assembled continuously from the telomere and are defined by promoter distance and strength, and by SIR3 dosage.

Authors:  H Renauld; O M Aparicio; P D Zierath; B L Billington; S K Chhablani; D E Gottschling
Journal:  Genes Dev       Date:  1993-07       Impact factor: 11.361

8.  Centromere function on minichromosomes isolated from budding yeast.

Authors:  J Kingsbury; D Koshland
Journal:  Mol Biol Cell       Date:  1993-08       Impact factor: 4.138

9.  Enhancement of telomere-plasmid segregation by the X-telomere associated sequence in Saccharomyces cerevisiae involves SIR2, SIR3, SIR4 and ABF1.

Authors:  S Enomoto; M S Longtine; J Berman
Journal:  Genetics       Date:  1994-03       Impact factor: 4.562

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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  8 in total

1.  Identification of a novel allele of SIR3 defective in the maintenance, but not the establishment, of silencing in Saccharomyces cerevisiae.

Authors:  S Enomoto; S D Johnston; J Berman
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

2.  Rap1 prevents telomere fusions by nonhomologous end joining.

Authors:  Benjamin Pardo; Stéphane Marcand
Journal:  EMBO J       Date:  2005-08-11       Impact factor: 11.598

3.  Chromatin assembly factor I contributes to the maintenance, but not the re-establishment, of silencing at the yeast silent mating loci.

Authors:  S Enomoto; J Berman
Journal:  Genes Dev       Date:  1998-01-15       Impact factor: 11.361

4.  CEN plasmid segregation is destabilized by tethered determinants of Ty 5 integration specificity: a role for double-strand breaks in CEN antagonism.

Authors:  Peter G Fuerst; Daniel F Voytas
Journal:  Chromosoma       Date:  2003-07-16       Impact factor: 4.316

5.  Telomere length regulation and telomeric chromatin require the nonsense-mediated mRNA decay pathway.

Authors:  J E Lew; S Enomoto; J Berman
Journal:  Mol Cell Biol       Date:  1998-10       Impact factor: 4.272

6.  Topoisomerase 2 is dispensable for the replication and segregation of small yeast artificial chromosomes (YACs).

Authors:  Jorge Cebrián; Estefanía Monturus; María-Luisa Martínez-Robles; Pablo Hernández; Dora B Krimer; Jorge B Schvartzman
Journal:  PLoS One       Date:  2014-08-12       Impact factor: 3.240

7.  Autonomously Replicating Linear Plasmids That Facilitate the Analysis of Replication Origin Function in Candida albicans.

Authors:  Swati Bijlani; Mathuravani A Thevandavakkam; Hung-Ji Tsai; Judith Berman
Journal:  mSphere       Date:  2019-03-06       Impact factor: 4.389

8.  Mammalian chromosome-telomere length dynamics.

Authors:  Amy R Klegarth; Dan T A Eisenberg
Journal:  R Soc Open Sci       Date:  2018-07-25       Impact factor: 2.963

  8 in total

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