Evidence map›Paper›PMID 26186223›Full record

ArticlePloS one2015

Mapping of the Sequences Directing Localization of the Drosophila Germ Cell-Expressed Protein (GCE).

Beata Greb-Markiewicz, Daria Sadowska, Natalia Surgut, Jakub Godlewski, Mirosław Zarębski, Andrzej Ożyhar

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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

9 citing papers in PubMed.

  1. Juvenile hormone receptor relies on conserved domain interfaces for dimerization-dependent activity.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

6 authors.

Beata Greb-MarkiewiczDepartment of Biochemistry, Faculty of Chemistry, Wrocław University of Technology, Wrocław, Poland.
Daria SadowskaDepartment of Biochemistry, Faculty of Chemistry, Wrocław University of Technology, Wrocław, Poland.
Natalia SurgutDepartment of Biochemistry, Faculty of Chemistry, Wrocław University of Technology, Wrocław, Poland.
Jakub GodlewskiDepartment of Neurosurgery, Brigham and Woman's Hospital, Harvard Medical School, Harvard Institute of Medicine, Boston, Massachusetts, United States of America.
Mirosław ZarębskiDepartment of Cell Biophysics, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland.
Andrzej OżyharDepartment of Biochemistry, Faculty of Chemistry, Wrocław University of Technology, Wrocław, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drosophila melanogaster germ cell-expressed protein (GCE) belongs to the family of bHLH-PAS transcription factors that are the regulators of gene expression networks that determine many physiological and developmental processes. GCE is a homolog of D. melanogaster methoprene tolerant protein (MET), a key mediator of anti-metamorphic signaling in insects and the putative juvenile hormone receptor. Recently, it has been shown that the functions of MET and GCE are only partially redundant and tissue specific. The ability of bHLH-PAS proteins to fulfill their function depends on proper intracellular trafficking, determined by specific sequences, i.e. the nuclear localization signal (NLS) and the nuclear export signal (NES). Nevertheless, until now no data has been published on the GCE intracellular shuttling and localization signals. We performed confocal microscopy analysis of the subcellular distribution of GCE fused with yellow fluorescent protein (YFP) and YFP-GCE derivatives which allowed us to characterize the details of the subcellular traffic of this protein. We demonstrate that GCE possess specific pattern of localization signals, only partially consistent with presented previously for MET. The presence of a strong NLS in the C-terminal part of GCE, seems to be unique and important feature of this protein. The intracellular localization of GCE appears to be determined by the NLSs localized in PAS-B domain and C-terminal fragment of GCE, and NESs localized in PAS-A, PAS-B domains and C-terminal fragment of GCE. NLSs activity can be modified by juvenile hormone (JH) and other partners, likely 14-3-3 proteins.

Indexed as

Sequence Analysis, ProteinAmino Acid SequenceAnimalsCell NucleusChlorocebus aethiopsCOS CellsDrosophila melanogasterDrosophila ProteinsHEK293 CellsHumansIntracellular SpaceJuvenile HormonesMolecular Sequence DataMutant ProteinsNuclear Export SignalsNuclear Localization SignalsDrosophila Proteinsgce protein, DrosophilaJuvenile HormonesMutant ProteinsNuclear Export SignalsNuclear Localization SignalsTranscription Factors

Identifiers

PMID26186223
PMCPMC4505938

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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.