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PMID: 10890982 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Forkhead Foxe3 maps to the dysgenetic lens locus and is critical in lens development and differentiation.

Genesis (New York, N.Y. : 2000) ·Vol. 27 ·No. 2 ·2000-06-00 ·Pages 81-93

Brownell I, Dirksen M, Jamrich M

Abstract

Here we report the isolation of a novel forkhead gene, Foxe3, that plays an important role in lens formation. During development Foxe3 is expressed in all undifferentiated lens tissues, and is turned off upon fiber cell differentiation. Foxe3 maps to a chromosomal region containing the dysgenetic lens (dyl) mutation. Mice homozygous for dyl display several defects in lens development. dyl mice also show altered patterns of crystallin expression suggesting a dysregulation of lens differentiation. We have identified mutations in Foxe3 that cosegregate with the dyl phenotype and are a likely cause of the mutant phenotype. Head ectoderm expression of Foxe3 is absent in Rx-/- and Small eye embryos indicating that Rx and Pax6 activity are necessary for Foxe3 expression.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Chromosome Mapping Embryonic and Fetal Development/genetics Forkhead Transcription Factors Gene Expression Regulation, Developmental Lens, Crystalline/embryology,physiology Mice Molecular Sequence Data Mutation Transcription Factors/genetics
Chemicals
Forkhead Transcription Factors Foxe3 protein, mouse Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Brownell I
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Dirksen M
Jamrich M
Article Info
Journal
Genesis (New York, N.Y. : 2000)
Abbr.
Genesis
ISSN
1526-954X
Published
2000-06-00
Pages
81-93
Language
English
Region
United States
NLM ID
100931242
Subset
IM
Grants
NEI NIH HHS · EY12163 · United States
NEI NIH HHS · EY12505 · United States
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