Evidence map›Paper›PMID 11923418›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2002

Regulated cationic channel function in Xenopus oocytes expressing Drosophila big brain.

Gina M Yanochko, Andrea J Yool

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

28 citing papers in PubMed, 70 citations in OpenAlex.

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  16. Article
  17. Emerging roles of aquaporins in relation to the physiology of blood-feeding arthropods.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2014
    Review
  18. Aquaporin homologs and water transport in the anal papillae of the larval mosquito, Aedes aegypti.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2012
    Article
  19. Article
  20. Endocytosis and intracellular trafficking of Notch and its ligands.Current topics in developmental biology · 2010
    Review
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

2 authors at 1 institution in 1 country.

Gina M YanochkoProgram in Pharmacology and Toxicology and Department of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona 85724-5051, USA.
Andrea J Yool
University of Arizona · US

Funding

STRUCTURAL BASIS OF ION CHANNEL FUNCTION IN AQUAPORIN-1R01GM059986 · NIGMS · UNIVERSITY OF ARIZONA · PI STAMER, W DANIEL · 2000 to 2007
$1.9M
TRAINING PROGRAM IN DEVELOPMENTAL NEUROSCIENCET32NS007363 · NINDS · UNIVERSITY OF ARIZONA · PI LEVINE, RICHARD B · 1993 to 1998
–
NIGMS NIH HHS R01 GM059986NIGMS NIH HHS R01 GM 59986NINDS NIH HHS T32 NS007363NINDS NIH HHS T32 NS-07363
6 · The paper itself

Abstract

Big brain (bib) is a neurogenic gene that when mutated causes defects in cell fate determination during Drosophila neurogenesis through an unknown mechanism. The protein Big Brain (BIB) has sequence identity with the major intrinsic protein family that includes the water- and ion-conducting aquaporin channels. We show here that BIB expressed heterologously in Xenopus oocytes provides a voltage-insensitive, nonselective cation channel function with permeability to K+ > Na+ >> tetraethylammonium. The conductance, activated in response to endogenous signaling pathways in BIB-expressing oocytes, is decreased after treatment with 20 microm insulin and is enhanced with 10 microm lavendustin A, a tyrosine kinase inhibitor. Western blot analysis confirms that BIB is tyrosine-phosphorylated. Both tyrosine phosphorylation and the potentiating effect of lavendustin A are removed by partial deletion of the C terminus (amino acids 317-700). Current activation is not observed in control oocytes or in oocytes expressing a nonfunctional mutant (BIB E71N) that appears to be expressed on the plasma membrane by confocal microscopy and Western blotting. These results indicate that BIB can participate in tyrosine kinase-regulated transmembrane signaling and may suggest a role for membrane depolarization in the neurogenic function of BIB in early development.

Indexed as

Drosophila ProteinsAnimalsCationsCell Membrane PermeabilityDose-Response Relationship, DrugDrosophilaEnzyme InhibitorsGene ExpressionInsulinIon ChannelsIon TransportMembrane PotentialsMembrane ProteinsMicroinjectionsMutagenesis, Site-DirectedOocytesbib protein, DrosophilaCationsDrosophila ProteinsEnzyme InhibitorsInsulinIon ChannelsMembrane ProteinsRNA, ComplementaryWater

Identifiers

PMID11923418
PMCPMC6758330
OpenAlexW2129774838

What OpenQuestion holds

Textmetadata
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.