PUBLICATION

Genetic control of single lumen formation in the zebrafish gut

Authors
Bagnat, M., Cheung, I.D., Mostov, K.E., and Stainier, D.Y.
ID
ZDB-PUB-070726-15
Date
2007
Source
Nature cell biology   9(8): 954-960 (Journal)
Registered Authors
Bagnat, Michel, Stainier, Didier
Keywords
none
MeSH Terms
  • Intestines*/abnormalities
  • Intestines*/anatomy & histology
  • Intestines*/embryology
  • Sodium-Potassium-Exchanging ATPase/metabolism
  • Ion Channels/metabolism
  • Hepatocyte Nuclear Factor 1-beta/genetics
  • Hepatocyte Nuclear Factor 1-beta/metabolism*
  • In Situ Hybridization
  • Zebrafish*/anatomy & histology
  • Zebrafish*/embryology
  • Cells, Cultured
  • Ion Transport/physiology
  • Animals, Genetically Modified
  • Membrane Proteins/metabolism
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
  • Morphogenesis*
  • Molecular Sequence Data
  • Animals
  • Claudins
(all 20)
PubMed
17632505 Full text @ Nat. Cell Biol.
Abstract
Most organs consist of networks of interconnected tubes that serve as conduits to transport fluid and cells and act as physiological barriers between compartments. Biological tubes are assembled through very diverse developmental processes that generate structures of different shapes and sizes. Nevertheless, all biological tubes invariably possess one single lumen. The mechanisms responsible for single lumen specification are not known. Here we show that zebrafish mutants for the MODY5 and familial GCKD gene tcf2 (also known as vhnf1) fail to specify a single lumen in their gut tube and instead develop multiple lumens. We show that Tcf2 controls single lumen formation by regulating claudin15 and Na(+)/K(+)-ATPase expression. Our in vivo and in vitro results indicate that Claudin15 functions in paracellular ion transport to specify single lumen formation. This work shows that single lumen formation is genetically controlled and appears to be driven by the accumulation of fluid.
Genes / Markers
Figures
No images available
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
b781
    Point Mutation
    gz4TgTransgenic Insertion
      hi2169TgTransgenic Insertion
      m520
        Point Mutation
        m567
          Point Mutation
          s854TgTransgenic Insertion
            1 - 6 of 6
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            Human Disease / Model
            No data available
            Sequence Targeting Reagents
            Target Reagent Reagent Type
            cldn15aMO1-cldn15aMRPHLNO
            oclnaMO1-oclnaMRPHLNO
            1 - 2 of 2
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            Fish
            Antibodies
            No data available
            Orthology
            Engineered Foreign Genes
            Marker Marker Type Name
            GFPEFGGFP
            1 - 1 of 1
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            Mapping