Evidence map›Paper›PMID 28380354›Full record

ArticleCell reports2017

The Drosophila hnRNP F/H Homolog Glorund Uses Two Distinct RNA-Binding Modes to Diversify Target Recognition.

Joel V Tamayo, Takamasa Teramoto, Seema Chatterjee, Traci M Tanaka Hall, Elizabeth R Gavis

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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  8. Translational Control during Developmental Transitions.Cold Spring Harbor perspectives in biology · 2019
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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

5 authors at 2 institutions in 1 country.

Joel V TamayoDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Takamasa TeramotoEpigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.
Seema ChatterjeeDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Traci M Tanaka HallEpigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA. Electronic address: hall4@niehs.nih.gov.
Elizabeth R GavisDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. Electronic address: gavis@princeton.edu.
Princeton University · USNational Institutes of Health · US

Funding

Structural Studies Of Post-Transcriptional Gene RegulationZIAES050165 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI HALL, TRACI M · 2009 to 2025
$45.7M
Translational Regulation of Patterning in DrosphilaR01GM061107 · NIGMS · PRINCETON UNIVERSITY · PI GAVIS, ELIZABETH R · 2001 to 2017
$5.2M
Intramural NIH HHS ZIA ES050165NIGMS NIH HHS R01 GM061107
6 · The paper itself

Abstract

The Drosophila hnRNP F/H homolog, Glorund (Glo), regulates nanos mRNA translation by interacting with a structured UA-rich motif in the nanos 3' untranslated region. Glo regulates additional RNAs, however, and mammalian homologs bind G-tract sequences to regulate alternative splicing, suggesting that Glo also recognizes G-tract RNA. To gain insight into how Glo recognizes both structured UA-rich and G-tract RNAs, we used mutational analysis guided by crystal structures of Glo's RNA-binding domains and identified two discrete RNA-binding surfaces that allow Glo to recognize both RNA motifs. By engineering Glo variants that favor a single RNA-binding mode, we show that a subset of Glo's functions in vivo is mediated solely by the G-tract binding mode, whereas regulation of nanos requires both recognition modes. Our findings suggest a molecular mechanism for the evolution of dual RNA motif recognition in Glo that may be applied to understanding the functional diversity of other RNA-binding proteins.

Indexed as

Alternative SplicingAmino Acid SequenceAnimalsDrosophila melanogasterDrosophila ProteinsFemaleHeterogeneous-Nuclear Ribonucleoprotein Group F-HMutationNucleotide MotifsOocytesOvaryProtein BiosynthesisRNARNA-Binding ProteinsTransforming Growth Factor alphaDrosophila ProteinsGlo protein, Drosophilagrk protein, DrosophilaHeterogeneous-Nuclear Ribonucleoprotein Group F-Hnos protein, DrosophilaRNARNA-Binding ProteinsTransforming Growth Factor alphadevelopmentDrosophilaGlorundhnRNPhnRNP FhnRNP Hnanospost-transcriptional regulationRNA-binding proteintranslational controltranslational repressor

Identifiers

PMID28380354
PMCPMC5392723
OpenAlexW2604814645

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.