Evidence map›Paper›PMID 23394947›Full record

ArticleCell2013

A systematic mammalian genetic interaction map reveals pathways underlying ricin susceptibility.

Michael C Bassik, Martin Kampmann, Robert Jan Lebbink, Shuyi Wang, Marco Y Hein, Ina Poser, Jimena Weibezahn, Max A Horlbeck, Siyuan Chen, Matthias Mann and 4 more

Abstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 243 papers.

0numbers the graph read from it
0cells of the map it votes in
243citing 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

243 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Scaling perturbations: beyond genome-scale CRISPR screens.bioRxiv : the preprint server for biology · 2026
    Article
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  20. Review

183 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Michael C BassikDepartment of Cellular and Molecular Pharmacology, California Institute for Quantitative Biomedical Research and Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94122, USA. bassik@cmp.ucsf.edu
Martin Kampmann
Robert Jan Lebbink
Shuyi Wang
Marco Y Hein
Ina Poser
Jimena Weibezahn
Max A Horlbeck
Siyuan Chen
Matthias Mann
Anthony A Hyman
Emily M Leproust
Michael T McManus
Jonathan S Weissman

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007618 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S · 1985 to 2020
$29.6M
Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2003 to 2019
$21.8M
Bay Area Cancer Target Discovery and Development NetworkU01CA168370 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCCORMICK, FRANK PATRICK, MCMANUS, MICHAEL T · 2012 to 2016
$3.9M
Integrative Program in Complex Biological System (ipCBS)T32EB009383 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARSHALL, WALLACE, WEINER, ORION D · 2009 to 2022
$3.2M
New Frontiers for Small RNA TherapiesR01GM080783 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCMANUS, MICHAEL T · 2007 to 2011
$1.5M
Howard Hughes Medical InstituteNCI NIH HHS 1U01CA168370-01NCI NIH HHS U01 CA168370NIBIB NIH HHS T32 EB009383NIDDK NIH HHS P30 DK063720NIGMS NIH HHS R01 GM80783NIGMS NIH HHS T32 GM007618
6 · The paper itself

Abstract

Genetic interaction (GI) maps, comprising pairwise measures of how strongly the function of one gene depends on the presence of a second, have enabled the systematic exploration of gene function in microorganisms. Here, we present a two-stage strategy to construct high-density GI maps in mammalian cells. First, we use ultracomplex pooled shRNA libraries (25 shRNAs/gene) to identify high-confidence hit genes for a given phenotype and effective shRNAs. We then construct double-shRNA libraries from these to systematically measure GIs between hits. A GI map focused on ricin susceptibility broadly recapitulates known pathways and provides many unexpected insights. These include a noncanonical role for COPI, a previously uncharacterized protein complex affecting toxin clearance, a specialized role for the ribosomal protein RPS25, and functionally distinct mammalian TRAPP complexes. The ability to rapidly generate mammalian GI maps provides a potentially transformative tool for defining gene function and designing combination therapies based on synergistic pairs.

Indexed as

Biological TransportEpistasis, GeneticAtorvastatinBromodomain Containing ProteinsCarrier ProteinsCell Line, TumorCoat Protein Complex IEndoplasmic ReticulumHeptanoic AcidsHumansMembrane ProteinsProto-Oncogene ProteinsPyrrolesRibosomal ProteinsRicinRNA, Small InterferingAtorvastatinBromodomain Containing ProteinsC17orf75 protein, humanCarrier ProteinsCoat Protein Complex IHeptanoic AcidsMembrane ProteinsProto-Oncogene ProteinsPyrrolesRibosomal ProteinsRicinRNA, Small InterferingRPS25 protein, humantransport protein particle, TRAPPVesicular Transport ProteinsWDR11 protein, human

Identifiers

PMID23394947
PMCPMC3652613

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.