Evidence map›Paper›PMID 23050238›Full record

ArticleG3 (Bethesda, Md.)2012

Functional analysis with a barcoder yeast gene overexpression system.

Alison C Douglas, Andrew M Smith, Sara Sharifpoor, Zhun Yan, Tanja Durbic, Lawrence E Heisler, Anna Y Lee, Owen Ryan, Hendrikje Göttert, Anu Surendra and 5 more

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
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

52 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. International journal of molecular sciences · 2023
    Article
  8. A Toolkit for Precise, Multigene Control inACS synthetic biology · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Lithium Chloride Sensitivity in Yeast and Regulation of Translation.International journal of molecular sciences · 2020
    Article
  20. Article
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

15 authors.

Alison C DouglasDepartment of Molecular Genetics, University of Toronto, Ontario M5S 1A8, Canada.
Andrew M Smith
Sara Sharifpoor
Zhun Yan
Tanja Durbic
Lawrence E Heisler
Anna Y Lee
Owen Ryan
Hendrikje Göttert
Anu Surendra
Dewald van Dyk
Guri Giaever
Charles Boone
Corey Nislow
Brenda J Andrews

Funding

Technology to Identify and Assay Chemical Genomic ProbesR01HG003317 · NHGRI · STANFORD UNIVERSITY · PI DAVIS, RONALD WAYNE · 2004 to 2012
$9.1M
Mapping the reference genetic network of a eukaryotic cellR01HG005853 · NHGRI · UNIVERSITY OF TORONTO · PI ANDREWS, BRENDA JEAN, BOONE, CHARLES · 2010 to 2025
$7.6M
CIHR MOP-102629CIHR MOP-114929CIHR MOP-81340NHGRI NIH HHS R01 HG003317NHGRI NIH HHS R01 HG003317-08NHGRI NIH HHS R01 HG005853NHGRI NIH HHS R01 HG005853-02
6 · The paper itself

Abstract

Systematic analysis of gene overexpression phenotypes provides an insight into gene function, enzyme targets, and biological pathways. Here, we describe a novel functional genomics platform that enables a highly parallel and systematic assessment of overexpression phenotypes in pooled cultures. First, we constructed a genome-level collection of ~5100 yeast barcoder strains, each of which carries a unique barcode, enabling pooled fitness assays with a barcode microarray or sequencing readout. Second, we constructed a yeast open reading frame (ORF) galactose-induced overexpression array by generating a genome-wide set of yeast transformants, each of which carries an individual plasmid-born and sequence-verified ORF derived from the Saccharomyces cerevisiae full-length EXpression-ready (FLEX) collection. We combined these collections genetically using synthetic genetic array methodology, generating ~5100 strains, each of which is barcoded and overexpresses a specific ORF, a set we termed "barFLEX." Additional synthetic genetic array allows the barFLEX collection to be moved into different genetic backgrounds. As a proof-of-principle, we describe the properties of the barFLEX overexpression collection and its application in synthetic dosage lethality studies under different environmental conditions.

Indexed as

DNA Barcoding, TaxonomicGene ExpressionComputational BiologyFungal ProteinsGene Expression ProfilingGenome, FungalGenomicsSaccharomyces cerevisiaeFungal ProteinsbarcodersbarFLEX arraygene overexpressionsynthetic dosage lethality

Identifiers

PMID23050238
PMCPMC3464120

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.