Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene

Weidong Wang, Thomas R Van De Water, Thomas Lufkin

Research output: Contribution to journalArticle

130 Citations (Scopus)

Abstract

The Hmx homeobox gene family is of ancient origin, being present in species as diverse as Drosophila, sea urchin and mammals. The three members of the murine Hmx family, designated Hmx1, Hmx2 and Hmx3, are expressed in tissues that suggest a common functional role in sensory organ development and pregnancy. Hmx3 is one of the earliest markers for vestibular inner ear development during embryogenesis, and is also upregulated in the myometrium of the uterus during pregnancy. Targeted disruption of the Hmx3 gene results in mice with abnormal circling behavior and severe vestibular defects owing to a depletion of sensory cells in the saccule and utricle, and a complete loss of the horizontal semicircular canal crista, as well as a fusion of the utricle and saccule endolymphatic spaces into a common utriculosaccular cavity. Both the sensory and secretory epithelium of the cochlear duct appear normal in the Hmx3 null animals. The majority of Hmx3 null females have a reproductive defect. Hmx3 null females can be fertilized and their embryos undergo normal preimplantation development, but the embryos fail to implant successfully in the Hmx3 null uterus and subsequently die. Transfer of preimplantation embryos from mutant Hmx3 uterine horns to wild-type pseudopregnant females results in successful pregnancy, indicating a failure of the Hmx3 null uterus to support normal post-implantation pregnancy. Molecular analysis revealed the perturbation of Hmx, Wnt and LIF gene expression in the Hmx3 null uterus. Interestingly, expression of both Hmx1 and Hmx2 is downregulated in the Hmx3 null uterus, suggesting a hierarchical relationship among the three Hmx genes during pregnancy.

Original languageEnglish
Pages (from-to)621-634
Number of pages14
JournalDevelopment
Volume125
Issue number4
StatePublished - Feb 1 1998
Externally publishedYes

Fingerprint

Homeobox Genes
Inner Ear
Uterus
Mothers
Pregnancy
Saccule and Utricle
Embryonic Development
Cochlear Duct
Semicircular Canals
Sea Urchins
Myometrium
Blastocyst
Genes
Drosophila
Mammals
Down-Regulation
Embryonic Structures
Epithelium
Gene Expression

Keywords

  • Gene knockout
  • Homeobox gene
  • Inner ear
  • Mouse
  • Pregnancy

ASJC Scopus subject areas

  • Anatomy
  • Cell Biology

Cite this

Wang, W., Van De Water, T. R., & Lufkin, T. (1998). Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene. Development, 125(4), 621-634.

Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene. / Wang, Weidong; Van De Water, Thomas R; Lufkin, Thomas.

In: Development, Vol. 125, No. 4, 01.02.1998, p. 621-634.

Research output: Contribution to journalArticle

Wang, W, Van De Water, TR & Lufkin, T 1998, 'Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene', Development, vol. 125, no. 4, pp. 621-634.
Wang W, Van De Water TR, Lufkin T. Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene. Development. 1998 Feb 1;125(4):621-634.
Wang, Weidong ; Van De Water, Thomas R ; Lufkin, Thomas. / Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene. In: Development. 1998 ; Vol. 125, No. 4. pp. 621-634.
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