Evidence map›Paper›PMID 20643119›Full record

ArticleDevelopmental biology2010

The ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos.

Sherry Aw, Joseph C Koster, Wade Pearson, Colin G Nichols, Nian-Qing Shi, Katia Carneiro, Michael Levin

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Review
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  5. Electrochemical Devices in Cutaneous Wound Healing.Bioengineering (Basel, Switzerland) · 2023
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  10. HCN2 Channel-Induced Rescue of Brain TeratogenesisFrontiers in cellular neuroscience · 2020
    Article
  11. Article
  12. Review
  13. Review
  14. TGF-β Family Signaling in Early Vertebrate Development.Cold Spring Harbor perspectives in biology · 2018
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  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

7 authors at 3 institutions in 1 country.

Sherry AwCenter for Regenerative and Developmental Biology, and Biology Department, Tufts University, Medford, MA 02155, USA.
Joseph C Koster
Wade Pearson
Colin G Nichols
Nian-Qing Shi
Katia Carneiro
Michael Levin
Tufts University · USWashington University in St. Louis · USUniversity of Wisconsin–Madison · US

Funding

Novel Mechanism of Induction of Eye Tissue: Katp Channel ModulationR01EY018168 · NEI · TUFTS UNIVERSITY MEDFORD · PI LEVIN, MICHAEL · 2008 to 2010
$1.1M
Bioelectrical Controls of MorphogenesisR01GM077425 · NIGMS · TUFTS UNIVERSITY MEDFORD · PI LEVIN, MICHAEL · 2007 to 2010
$1.1M
Mechanisms underlie inverse gender discrepancy in ischemic protectionR21HL093626 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI SHI, NIAN-QING · 2009 to 2010
$408k
NEI NIH HHS R01 EY018168NHLBI NIH HHS HL093626NHLBI NIH HHS R21 HL093626NIGMS NIH HHS R01 GM077425NIGMS NIH HHS R01-GM077425
6 · The paper itself

Abstract

Consistent left-right asymmetry requires specific ion currents. We characterize a novel laterality determinant in Xenopus laevis: the ATP-sensitive K(+)-channel (K(ATP)). Expression of specific dominant-negative mutants of the Xenopus Kir6.1 pore subunit of the K(ATP) channel induced randomization of asymmetric organ positioning. Spatio-temporally controlled loss-of-function experiments revealed that the K(ATP) channel functions asymmetrically in LR patterning during very early cleavage stages, and also symmetrically during the early blastula stages, a period when heretofore largely unknown events transmit LR patterning cues. Blocking K(ATP) channel activity randomizes the expression of the left-sided transcription of Nodal. Immunofluorescence analysis revealed that XKir6.1 is localized to basal membranes on the blastocoel roof and cell-cell junctions. A tight junction integrity assay showed that K(ATP) channels are required for proper tight junction function in early Xenopus embryos. We also present evidence that this function may be conserved to the chick, as inhibition of K(ATP) in the primitive streak of chick embryos randomizes the expression of the left-sided gene Sonic hedgehog. We propose a model by which K(ATP) channels control LR patterning via regulation of tight junctions.

Indexed as

Body PatterningAnimalsBlastomeresChick EmbryoKATP ChannelsPotassiumPotassium Channels, Inwardly RectifyingTight JunctionsXenopus laevisKATP ChannelsPotassiumPotassium Channels, Inwardly RectifyinguK-ATP-1 potassium channel

Identifiers

PMID20643119
PMCPMC2937067
OpenAlexW2073153876

What OpenQuestion holds

Textmetadata
LicenceTDM
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.