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

S Enomoto, M S Longtine, J Berman

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

We have previously shown that circular replicating plasmids that carry yeast telomere repeat sequence (TG1-3) tracts segregate efficiently relative to analogous plasmids lacking the TG1-3 tract and this efficient segregation is dependent upon RAP1. While a long TG1-3 tract is sufficient to improve plasmid segregation, the segregation efficiency of telomere plasmids (TEL-plasmids) is enhanced when the X-Telomere Associated Sequence (X-TAS) is also included on the plasmids. We now demonstrate that the enhancement of TEL-plasmid segregation by the X-TAS depends on SIR2, SIR3, SIR4 and ABF1 in trans and requires the Abf1p-binding site within the X-TAS. Mutation of the Abf1p-binding site within the X-TAS results in TEL-plasmids that are no longer affected by mutations in SIR2, SIR3 or SIR4, despite the fact that other Abf1p-binding sites are present on the plasmid. Mutation of the ARS consensus sequence within the X-TAS converts the X-TAS from an enhancer element to a negative element that interferes with TEL-plasmid segregation in a SIR-dependent manner. Thus, telomere associated sequences interact with TG1-3 tracts on the plasmid, suggesting that the TASs have an active role in modulating telomere function.

Original languageEnglish
Pages (from-to)757-67
Number of pages11
JournalGenetics
Volume136
Issue number3
DOIs
StatePublished - Mar 1994
Externally publishedYes

Funding

FundersFunder number
National Institute of General Medical SciencesR01GM038626

    Keywords

    • Base Sequence
    • Binding Sites/genetics
    • DNA, Fungal/genetics
    • DNA, Recombinant/genetics
    • Escherichia coli/genetics
    • Genes, Fungal
    • Molecular Sequence Data
    • Mutagenesis, Site-Directed
    • Plasmids
    • Saccharomyces cerevisiae/genetics
    • Telomere/metabolism

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