Evidence map›Paper›PMID 17164420›Full record

ArticleDevelopment (Cambridge, England)2007

A pump-independent function of the Na,K-ATPase is required for epithelial junction function and tracheal tube-size control.

Sarah M Paul, Michael J Palladino, Greg J Beitel

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Development (Cambridge, England), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

48 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
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  9. Review
  10. Article
  11. Caste-Specific Expression of NaNeotropical entomology · 2018
    Article
  12. Fibroblast-SpecificJournal of the American Society of Nephrology : JASN · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Occluding junctions of invertebrate epithelia.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2016
    Review
  18. Article
  19. Article
  20. Article
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

3 authors at 2 institutions in 1 country.

Sarah M PaulDepartment of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208, USA.
Michael J Palladino
Greg J Beitel
Northwestern University · USUniversity of Wisconsin–Madison · US

Funding

Neurogenetics of TS-Paralytic Mutants in DrosophilaR01NS015390 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI GANETZKY, BARRY S · 1985 to 2011
$4.5M
Understanding the Mechanisms of NeuropathogenesisR01AG025046 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PALLADINO, MICHAEL JOHN · 2006 to 2010
$1.5M
Tube-size control by the Na K ATPase &septate junctionsR01GM069540 · NIGMS · NORTHWESTERN UNIVERSITY · PI BEITEL, GREG J · 2004 to 2008
$1.3M
NIA NIH HHS R01 AG025046NIGMS NIH HHS R01 GM069540NINDS NIH HHS R01 NS015390NINDS NIH HHS R01 NS15390
6 · The paper itself

Abstract

The heterodimeric Na,K-ATPase has been implicated in vertebrate and invertebrate epithelial cell junctions, morphogenesis and oncogenesis, but the mechanisms involved are unclear. We previously showed that the Drosophila Na,K-ATPase is required for septate junction (SJ) formation and that of the three beta-subunit loci, only Nrv2 isoforms support epithelial SJ barrier function and tracheal tube-size control. Here we show that Nrv1 is endogenously co-expressed with Nrv2 in the epidermis and tracheal system, but Nrv1 has a basolateral localization and appears to be excluded from the Nrv2-containing SJs. When the normally neuronal Nrv3 is expressed in epithelial cells, it does not associate with SJs. Thus, the beta-subunit is a key determinant of Na,K-ATPase subcellular localization as well as function. However, localization of the Na,K-ATPase to SJs is not sufficient for junctional activity because although several Nrv2/Nrv3 chimeric beta-subunits localize to SJs, only those containing the extracellular domain of Nrv2 have junctional activity. Junctional activity is also specific to different alpha-subunit isoforms, with only some isoforms from the major alpha-subunit locus being able to provide full barrier function and produce normal tracheal tubes. Importantly, mutations predicted to inactivate ATPalpha catalytic function do not compromise junctional activity, demonstrating that the Drosophila Na,K-ATPase has an ion-pump-independent role in junction formation and tracheal morphogenesis. These results define new functions for the intensively studied Na,K-ATPase. Strikingly, the rat alpha1 isoform has full junctional activity and can rescue Atpalpha-null mutants to viability, suggesting that the Na,K-ATPase has an evolutionarily conserved role in junction formation and function.

Indexed as

Alternative SplicingAnimalsAnimals, Genetically ModifiedDrosophilaDrosophila ProteinsEmbryo, NonmammalianEpitheliumGlycoproteinsIntercellular JunctionsIsoenzymesMutationNerve Tissue ProteinsProtein Structure, TertiarySodium-Potassium-Exchanging ATPaseTracheaDrosophila ProteinsGlycoproteinsIsoenzymesNerve Tissue Proteinsnrv1 protein, DrosophilaNrv2 protein, DrosophilaNrv3 protein, DrosophilaSodium-Potassium-Exchanging ATPase

Identifiers

PMID17164420
PMCPMC1955469
OpenAlexW2056466716

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.