Evidence map›Paper›PMID 18453744›Full record

ArticleCellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology2008

KCNQ1 and KCNE1 K+ channel components are involved in early left-right patterning in Xenopus laevis embryos.

Junji Morokuma, Douglas Blackiston, Michael Levin

Open access · bronzeAbstract read
In one paragraph

Article in Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.6field-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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Laterality defects are influenced by timing of treatments and animal model.Differentiation; research in biological diversity · 2012
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  14. Biofield Physiology: A Framework for an Emerging Discipline.Global advances in health and medicine · 2015
    Review
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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

3 authors at 1 institution in 1 country.

Junji MorokumaCenter for Regenerative and Developmental Biology, Forsyth Institute, Developmental Biology Department, Harvard School of Dental Medicine, Boston, MA 02115, USA.
Douglas Blackiston
Michael Levin
California Institute for Regenerative Medicine · US

Funding

FORSYTH POSTDOCTORAL TRAINING IN ORAL HEALTH RESEARCHT32DE007327 · NIDCR · FORSYTH INSTITUTE · PI VAN DYKE, THOMAS ELLIOTT · 2001 to 2015
$3.5M
Bioelectrical Controls of MorphogenesisR01GM077425 · NIGMS · TUFTS UNIVERSITY MEDFORD · PI LEVIN, MICHAEL · 2007 to 2010
$1.1M
NCI NIH HHS CO6RR11244NIDCR NIH HHS 5T32DE007327-07NIDCR NIH HHS T32 DE007327NIGMS NIH HHS R01-GM07742NIGMS NIH HHS R01 GM077425
6 · The paper itself

Abstract

Several ion transporters have been implicated in left-right (LR) patterning. Here, we characterize a new component of the early bioelectrical circuit: the potassium channel KCNQ1 and its accessory subunit KCNE1. Having cloned the native Xenopus versions of both genes, we show that both are asymmetrically localized as maternal proteins during the first few cleavages of frog embryo development in a process dependent on microtubule and actin organization. Molecular loss-of-function using dominant negative constructs demonstrates that both gene products are required for normal LR asymmetry. We propose a model whereby these channels provide an exit path for K(+) ions brought in by the H(+),K(+)-ATPase. This physiological module thus allows the obligate but electroneutral H(+),K(+)-ATPase to generate an asymmetric voltage gradient on the left and right sides. Our data reveal a new, bioelectrical component of the mechanisms patterning a large-scale axis in vertebrate embryogenesis.

Indexed as

Body PatterningAnimalsCloning, MolecularCytoskeletonDrug Evaluation, PreclinicalEmbryo, NonmammalianKCNQ1 Potassium ChannelMaleOrgan SpecificityPotassium Channels, Voltage-GatedTime FactorsXenopus laevisXenopus ProteinsKCNE1 protein, XenopusKCNQ1 Potassium ChannelPotassium Channels, Voltage-GatedXenopus Proteins

Identifiers

PMID18453744
PMCPMC3632048
OpenAlexW2127726298

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.