Evidence map›Paper›PMID 9372937›Full record

ArticleMolecular and cellular biology1997

The yeast silent information regulator Sir4p anchors and partitions plasmids.

A Ansari, M R Gartenberg

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  8. Epigenetics in Saccharomyces cerevisiae.Cold Spring Harbor perspectives in biology · 2013
    Review
  9. Review
  10. Review
  11. Article
  12. Double rolling circle replication (DRCR) is recombinogenic.Genes to cells : devoted to molecular & cellular mechanisms · 2011
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

A AnsariDepartment of Pharmacology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway 08854, USA.
M R Gartenberg

Funding

Cohesin in Chromosome Architecture and Transcriptional ControlR01GM051402 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GARTENBERG, MARC R. · 1995 to 2022
$7.9M
CHROMOSOME ARCHITECTURER55GM051402 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GARTENBERG, MARC R. · 1994 to 1994
–
NIGMS NIH HHS GM 51402
6 · The paper itself

Abstract

Circular plasmids containing telomeric TG1-3 arrays or the HMR E silencer segregate efficiently between dividing cells of the yeast Saccharomyces cerevisiae. Subtelomeric X repeats augment the TG1-3 partitioning activity by a process that requires the SIR2, SIR3, and SIR4 genes, which are also required for silencer-based partitioning. Here we show that targeting Sir4p to DNA directly via fusion to the bacterial repressor LexA confers efficient mitotic segregation to otherwise unstable plasmids. The Sir4p partitioning activity resides within a 300-amino-acid region (residues 950 to 1262) which precedes the coiled-coil dimerization motif at the extreme carboxy end of the protein. Using a topology-based assay, we demonstrate that the partitioning domain also retards the axial rotation of LexA operators in vivo. The anchoring and partitioning properties of LexA-Sir4p chimeras persist despite the loss of the endogenous SIR genes, indicating that these functions are intrinsic to Sir4p and not to a complex of Sir factors. In contrast, inactivation of the Sir4p-interacting protein Rap1p reduces partitioning by a LexA-Sir4p fusion. The data are consistent with a model in which the partitioning and anchoring domain of Sir4p (PAD4 domain) attaches to a nuclear component that divides symmetrically between cells at mitosis; DNA linked to Sir4p by LexA serves as a reporter of protein movement in these experiments. We infer that the segregation behavior of telomere- and silencer-based plasmids is, in part, a consequence of these Sir4p-mediated interactions. The assays presented herein illustrate two novel approaches to monitor the intracellular dynamics of nuclear proteins.

Indexed as

Silent Information Regulator Proteins, Saccharomyces cerevisiaeBacterial ProteinsBase SequenceBinding SitesDNA, FungalFungal ProteinsGenes, FungalLexA Repressor ProteinModels, BiologicalNuclear ProteinsPlasmidsRecombinant Fusion ProteinsSaccharomyces cerevisiaeSerine EndopeptidasesBacterial ProteinsDNA, FungalFungal ProteinsLexA Repressor ProteinNuclear ProteinsRecombinant Fusion ProteinsSerine EndopeptidasesSilent Information Regulator Proteins, Saccharomyces cerevisiaeSIR4 protein, S cerevisiae

Identifiers

PMID9372937
PMCPMC232562
OpenAlexW2118231655

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.