Evidence map›Paper›PMID 26199285›Full record

ArticleG3 (Bethesda, Md.)2015

Reagent and Data Resources for Investigation of RNA Binding Protein Functions in Drosophila melanogaster Cultured Cells.

Stephanie E Mohr, Yanhui Hu, Kirstin Rudd, Michael Buckner, Quentin Gilly, Blake Foster, Katarzyna Sierzputowska, Aram Comjean, Bing Ye, Norbert Perrimon

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Dual Leucine Zipper Kinase Regulates Dscam Expression through a Noncanonical Function of the Cytoplasmic Poly(A)-Binding Protein.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
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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

10 authors at 3 institutions in 1 country.

Stephanie E MohrDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115 stephanie_mohr@hms.harvard.edu.
Yanhui HuDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Kirstin RuddDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Michael BucknerDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Quentin GillyDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Blake FosterDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Katarzyna SierzputowskaDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Aram ComjeanDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Bing YeLife Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109.
Norbert PerrimonDrosophila RNAi Screening Center, Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115 Howard Hughes Medical Institute, Boston, Massachusetts 02115.
Harvard University · USHoward Hughes Medical Institute · USUniversity of Michigan–Ann Arbor · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
New collections of dsRNAs and overexpression miRNA constructs to supplement RNAiR01GM067761 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI PERRIMON, NORBERT · 2003 to 2019
$15.5M
Howard Hughes Medical InstituteNCI NIH HHS 5 P30 CA06516NCI NIH HHS P30 CA006516NIGMS NIH HHS R01 GM067761
6 · The paper itself

Abstract

RNA binding proteins (RBPs) are involved in many cellular functions. To facilitate functional characterization of RBPs, we generated an RNA interference (RNAi) library for Drosophila cell-based screens comprising reagents targeting known or putative RBPs. To test the quality of the library and provide a baseline analysis of the effects of the RNAi reagents on viability, we screened the library using a total ATP assay and high-throughput imaging in Drosophila S2R+ cultured cells. The results are consistent with production of a high-quality library that will be useful for functional genomics studies using other assays. Altogether, we provide resources in the form of an initial curated list of Drosophila RBPs; an RNAi screening library we expect to be used with additional assays that address more specific biological questions; and total ATP and image data useful for comparison of those additional assay results with fundamental information such as effects of a given reagent in the library on cell viability. Importantly, we make the baseline data, including more than 200,000 images, easily accessible online.

Indexed as

Adenosine TriphosphateAnimalsCells, CulturedComputational BiologyDrosophila melanogasterDrosophila ProteinsGene LibraryGenomicsHigh-Throughput Screening AssaysRNA-Binding ProteinsRNA InterferenceRNA, Small InterferingAdenosine TriphosphateDrosophila ProteinsRNA-Binding ProteinsRNA, Small Interferingdata sharingDrosophilahigh-throughput screenRNA binding proteinRNAi

Identifiers

PMID26199285
PMCPMC4555228
OpenAlexW2107996050

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.