Literature DB >> 1956786

Analysis of the interactions of functional domains of a nuclear origin of replication from Saccharomyces cerevisiae.

S S Walker1, A K Malik, S Eisenberg.   

Abstract

We have determined that ARS121 is an efficient origin of replication on chromosome X of Saccharomyces cerevisiae. This origin is comprised of at least three distinct functional domains. One of these domains is the ARS121 core sequence (approximately 35 bp-long), which is essential for origin activity. This essential core contains an 11 bp sequence resembling (2 bp mismatch) the ARS consensus. Another important domain is an enhancer of DNA replication, which binds the OBF1 protein. The third domain, ATR (A/T-rich, approximately 72 bp), is auxiliary and works in either orientation, but only when located 3' to the essential core. When fused to the ARS121 core both the enhancer and the ATR domain act synergistically to enhance the activity of the origin. Furthermore, when fused to the essential core sequences of heterologous ARSs, ARS1 and ARS307, the auxiliary domains also appeared to stimulate synergistically origin function. These results suggest that (i) in order to elicit maximal origin activity all three domains have to interact and (ii) activation of the essential core sequences at different origins of replication may share a common mechanism.

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Year:  1991        PMID: 1956786      PMCID: PMC329136          DOI: 10.1093/nar/19.22.6255

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


  41 in total

1.  The localization of replication origins on ARS plasmids in S. cerevisiae.

Authors:  B J Brewer; W L Fangman
Journal:  Cell       Date:  1987-11-06       Impact factor: 41.582

2.  A mutant that affects the function of autonomously replicating sequences in yeast.

Authors:  P Sinha; V Chang; B K Tye
Journal:  J Mol Biol       Date:  1986-12-20       Impact factor: 5.469

3.  DNA sequence analysis of ARS elements from chromosome III of Saccharomyces cerevisiae: identification of a new conserved sequence.

Authors:  T G Palzkill; S G Oliver; C S Newlon
Journal:  Nucleic Acids Res       Date:  1986-08-11       Impact factor: 16.971

4.  Electron microscopic study of Saccharomyces cerevisiae rDNA chromatin replication.

Authors:  L D Saffer; O L Miller
Journal:  Mol Cell Biol       Date:  1986-04       Impact factor: 4.272

5.  A yeast silencer contains sequences that can promote autonomous plasmid replication and transcriptional activation.

Authors:  A H Brand; G Micklem; K Nasmyth
Journal:  Cell       Date:  1987-12-04       Impact factor: 41.582

6.  The in vivo replication origin of the yeast 2 microns plasmid.

Authors:  J A Huberman; L D Spotila; K A Nawotka; S M el-Assouli; L R Davis
Journal:  Cell       Date:  1987-11-06       Impact factor: 41.582

7.  Fine-structure analysis of the DNA sequence requirements for autonomous replication of Saccharomyces cerevisiae plasmids.

Authors:  A H Bouton; M M Smith
Journal:  Mol Cell Biol       Date:  1986-07       Impact factor: 4.272

8.  Structural requirements for the function of a yeast chromosomal replicator.

Authors:  S Kearsey
Journal:  Cell       Date:  1984-05       Impact factor: 41.582

9.  Mutants of S. cerevisiae defective in the maintenance of minichromosomes.

Authors:  G T Maine; P Sinha; B K Tye
Journal:  Genetics       Date:  1984-03       Impact factor: 4.562

10.  Two DNA-binding factors recognize specific sequences at silencers, upstream activating sequences, autonomously replicating sequences, and telomeres in Saccharomyces cerevisiae.

Authors:  A R Buchman; W J Kimmerly; J Rine; R D Kornberg
Journal:  Mol Cell Biol       Date:  1988-01       Impact factor: 4.272

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  33 in total

1.  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

2.  The ARS consensus sequence is required for chromosomal origin function in Saccharomyces cerevisiae.

Authors:  A M Deshpande; C S Newlon
Journal:  Mol Cell Biol       Date:  1992-10       Impact factor: 4.272

3.  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

4.  Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation of MCM subunits by a putative human homologue of Cdc7.

Authors:  N Sato; K Arai; H Masai
Journal:  EMBO J       Date:  1997-07-16       Impact factor: 11.598

5.  The B2 element of the Saccharomyces cerevisiae ARS1 origin of replication requires specific sequences to facilitate pre-RC formation.

Authors:  Gwendolyn M Wilmes; Stephen P Bell
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-26       Impact factor: 11.205

6.  The Ku-like protein from Saccharomyces cerevisiae is required in vitro for the assembly of a stable multiprotein complex at a eukaryotic origin of replication.

Authors:  N Shakibai; V Kumar; S Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

7.  Architecture of the yeast origin recognition complex bound to origins of DNA replication.

Authors:  D G Lee; S P Bell
Journal:  Mol Cell Biol       Date:  1997-12       Impact factor: 4.272

8.  The promoter of the Chinese hamster ovary dihydrofolate reductase gene regulates the activity of the local origin and helps define its boundaries.

Authors:  Swati Saha; Yujie Shan; Larry D Mesner; Joyce L Hamlin
Journal:  Genes Dev       Date:  2004-02-20       Impact factor: 11.361

9.  A replication map of a 61-kb circular derivative of Saccharomyces cerevisiae chromosome III.

Authors:  S A Greenfeder; C S Newlon
Journal:  Mol Biol Cell       Date:  1992-09       Impact factor: 4.138

10.  The origin recognition complex interacts with a bipartite DNA binding site within yeast replicators.

Authors:  H Rao; B Stillman
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-14       Impact factor: 11.205

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