Transgenic mouse model of X-linked cleft palate.

J. B. Wilson, M. W. Ferguson, N. A. Jenkins, L. F. Lock, N. G. Copeland, A. J. Levine

Research output: Contribution to journalArticle

26 Scopus citations

Abstract

A transgenic mouse line, PyLMP.5, exhibited a sex-linked lethality not observed in any other lines expressing the transgene. In this unique line, the transgene integrated into the X chromosome, yielding a simple tandem duplication of the insert sequences with minimal, if any, additional rearrangement of the cellular sequences. The predominant phenotype was a cleft secondary palate and neonatal lethality in males. Survival of females was dependent on the mouse strain background. The disrupted cellular sequences have been mapped to the proximal region of the mouse X chromosome. The disrupted locus may represent the mouse counterpart to a human locus mutated in an X-linked cleft secondary palate syndrome.

Original languageEnglish (US)
Pages (from-to)67-76
Number of pages10
JournalCell growth & differentiation : the molecular biology journal of the American Association for Cancer Research
Volume4
Issue number2
StatePublished - Feb 1993

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Fingerprint Dive into the research topics of 'Transgenic mouse model of X-linked cleft palate.'. Together they form a unique fingerprint.

Cite this