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Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

Krox20 is a zinc finger gene expressed in rhombomeres 3 and 5 during hindbrain development in vertebrates. Mice homozygous for a targeted mutation that deletes the majority of the Krox20 genes, including the zinc finger DNA-binding domain, died shortly after birth. The primary phenotype of the homozygous mutant animals was the loss of rhombomeres 3 and 5. This resulted in fusions of the trigeminal ganglion with the facial and vestibular ganglia, and of the superior ganglia of the glossopharyngeal and vagus nerves. These fusions resulted in a disorganization of the nerve roots of these ganglia as they entered the brain stem. These data demonstrate that Krox20 plays an essential role during development of the hindbrain and associated cranial sensory ganglia in mice.

Pubmed ID: 8224839

Authors

  • Swiatek PJ
  • Gridley T

Journal

Genes & development

Publication Data

November 16, 1993

Associated Grants

None

Mesh Terms

  • Amino Acid Sequence
  • Animals
  • Animals, Newborn
  • Base Sequence
  • Blastocyst
  • Blotting, Southern
  • DNA
  • DNA Primers
  • DNA-Binding Proteins
  • Early Growth Response Protein 2
  • Embryo, Mammalian
  • Female
  • Gene Deletion
  • Genes, Lethal
  • Genomic Library
  • Genotype
  • Glossopharyngeal Nerve
  • Homozygote
  • Male
  • Mice
  • Molecular Sequence Data
  • Phenotype
  • Polymerase Chain Reaction
  • Restriction Mapping
  • Rhombencephalon
  • Transcription Factors
  • Trigeminal Ganglion
  • Vagus Nerve
  • Zinc Fingers