Literature DB >> 6392851

Deletion mutations affecting autonomously replicating sequence ARS1 of Saccharomyces cerevisiae.

S E Celniker, K Sweder, F Srienc, J E Bailey, J L Campbell.   

Abstract

DNAs that contain specific yeast chromosomal sequences called ARSs transform Saccharomyces cerevisiae at high frequency and can replicate extrachromosomally as plasmids when introduced into S. cerevisiae by transformation. To determine the boundaries of the minimal sequences required for autonomous replication in S. cerevisiae, we have carried out in vitro mutagenesis of the first chromosomal ARS described, ARS1. Rather than identifying a distinct and continuous segment that mediates the ARS+ phenotype, we find three different functional domains within ARS1. We define domain A as the 11-base-pair (bp) sequence that is also found at most other ARS regions. It is necessary but not sufficient for high-frequency transformation. Domain B, which cannot mediate high-frequency transformation, or replicate by itself, is required for efficient, stable replication of plasmids containing domain A. Domain B, as we define it, is continuous with domain A in ARS1, but insertions of 4 bp between the two do not affect replication. The extent of domain B has an upper limit of 109 bp and a lower limit of 46 bp in size. There is no obvious sequence homology between domain B of ARS1 and any other ARS sequence. Finally, domain C is defined on the basis of our deletions as at least 200 bp flanking domain A on the opposite side from domain B and is also required for the stability of domain A in S. cerevisiae. The effect of deletions of domain C can be observed only in the absence of domain B, at least by the assays used in the current study, and the significance of this finding is discussed.

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Year:  1984        PMID: 6392851      PMCID: PMC369077          DOI: 10.1128/mcb.4.11.2455-2466.1984

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


  42 in total

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3.  Extracellular nucleases of pseudomonas BAL 31. III. Use of the double-strand deoxyriboexonuclease activity as the basis of a convenient method for the mapping of fragments of DNA produced by cleavage with restriction enzymes.

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Journal:  Nucleic Acids Res       Date:  1978-05       Impact factor: 16.971

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Authors:  S Scherer; R W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

5.  Isolation and characterisation of a yeast chromosomal replicator.

Authors:  D T Stinchcomb; K Struhl; R W Davis
Journal:  Nature       Date:  1979-11-01       Impact factor: 49.962

6.  Sequencing end-labeled DNA with base-specific chemical cleavages.

Authors:  A M Maxam; W Gilbert
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

7.  Isolation of chromosomal origins of replication in yeast.

Authors:  D Beach; M Piper; S Shall
Journal:  Nature       Date:  1980-03-13       Impact factor: 49.962

8.  High-frequency transformation of yeast: autonomous replication of hybrid DNA molecules.

Authors:  K Struhl; D T Stinchcomb; S Scherer; R W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1979-03       Impact factor: 11.205

9.  Characterization of an improved in vitro DNA replication system for Escherichia coli plasmids.

Authors:  S E Conrad; J L Campbell
Journal:  Nucleic Acids Res       Date:  1979-07-25       Impact factor: 16.971

10.  High-frequency transformation of yeast by plasmids containing the cloned yeast ARG4 gene.

Authors:  C L Hsiao; J Carbon
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

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  103 in total

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2.  Functional equivalency and diversity of cis-acting elements among yeast replication origins.

Authors:  S Lin; D Kowalski
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

3.  The phenotype of the minichromosome maintenance mutant mcm3 is characteristic of mutants defective in DNA replication.

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Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

4.  The organized chromatin domain of the repressed yeast a cell-specific gene STE6 contains two molecules of the corepressor Tup1p per nucleosome.

Authors:  C E Ducker; R T Simpson
Journal:  EMBO J       Date:  2000-02-01       Impact factor: 11.598

5.  At least three distinct proteins are necessary for the reconstitution of a specific multiprotein complex at a eukaryotic chromosomal origin of replication.

Authors:  H G Estes; B S Robinson; S Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

Review 6.  In search of the holy replicator.

Authors:  David M Gilbert
Journal:  Nat Rev Mol Cell Biol       Date:  2004-10       Impact factor: 94.444

7.  An ARS/silencer binding factor also activates two ribosomal protein genes in yeast.

Authors:  J C Dorsman; M M Doorenbosch; C T Maurer; J H de Winde; W H Mager; R J Planta; L A Grivell
Journal:  Nucleic Acids Res       Date:  1989-07-11       Impact factor: 16.971

8.  Interaction of the H4 autonomously replicating sequence core consensus sequence and its 3'-flanking domain.

Authors:  S G Holmes; M M Smith
Journal:  Mol Cell Biol       Date:  1989-12       Impact factor: 4.272

9.  Effect of ARS1 mutations on chromosome stability in Saccharomyces cerevisiae.

Authors:  F Srienc; J E Bailey; J L Campbell
Journal:  Mol Cell Biol       Date:  1985-07       Impact factor: 4.272

10.  Repetitive sequence variation and dynamics in the ribosomal DNA array of Saccharomyces cerevisiae as revealed by whole-genome resequencing.

Authors:  Stephen A James; Michael J T O'Kelly; David M Carter; Robert P Davey; Alexander van Oudenaarden; Ian N Roberts
Journal:  Genome Res       Date:  2009-01-13       Impact factor: 9.043

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