Isolation of a New Homeobox Gene Belonging to the Pitx/Rieg Family: Expression During Lens Development and Mapping to the Aphakia Region on Mouse Chromosome 19

• Published in: Human molecular genetics Vol. 6; no. 12; pp. 2109 - 2116
• Main Authors: Semina, Elena V., Reiter, Rebecca S., Murray, Jeffrey C.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01-11-1997
• Subjects: Amino Acid Sequence; Animals; Aphakia - genetics; Base Sequence; Biological and medical sciences; Chromosome Mapping; Classical genetics, quantitative genetics, hybrids; DNA, Complementary - isolation & purification; Embryonic and Fetal Development - genetics; Exons; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Developmental; Genes, Homeobox; Genetics of eukaryotes. Biological and molecular evolution; Homeobox Protein PITX2; Homeodomain Proteins - biosynthesis; Homeodomain Proteins - genetics; Introns; Lens, Crystalline - growth & development; Mice; Mice, Inbred C57BL; Molecular Sequence Data; Multigene Family; Mutation; Nuclear Proteins; Paired Box Transcription Factors; Transcription Factors - biosynthesis; Transcription Factors - genetics; Vertebrata; Genetic mapping; Chromosome 19; Embryonic development; Nucleotide sequence; Rodentia; Homology; Gene expression; Congenital disease; Vertebrata; Mammalia; Mouse; Malformation; Homeotic gene; Multigene family; Lens; Mutation
• ISSN: 0964-6906; 1460-2083
• DOI: 10.1093/hmg/6.12.2109

We recently reported the positional cloning of a homeobox gene involved in the pathogenesis of Rieger syndrome, RIEG1, and its mouse homolog, Rieg1. Rieg1 (also independently described as Pitx2) is highly homologous to the Ptx1/Potx gene product, suggesting that there may be additional members of this novel Pitx family. The Pitx genes play an important role in eye, tooth, pituitary and umbilical region development as evidenced by Rieger syndrome and iris hypoplasia phenotypes, resulting from mutations in the RIEG1 gene and by expression studies. In order to characterize further the Pitx gene family we searched mouse cDNA libraries to identify additional members. A new gene was isolated which encodes a homeoprotein with strong homology to the other Pitx proteins and 97–100% identity in the homeodomain itself, suggesting that this is a third member of the family, Pitx3. In whole mount in situ hybridization on mouse embryos ranging from 8.5 to 11.5 days post-coitum (d.p.c.), Pitx3 mRNA was seen only in the developing lens starting at day 11. Hybridization on cross-sections revealed strong signals in the lens vesicle in 11 d.p.c. embryos and throughout the lens, particularly in the anterior epithelium and equator region in 15 d.p.c. embryos. Pitx3 was mapped close to aphakia on mouse chromosome 19. The aphakia homozygous mouse is characterized by small eyes lacking a lens, which fail to develop beyond 11 d.p.c. These data make Pitx3 a strong candidate gene for the aphakia phenotype in the mouse and suggest a role for the human homolog in congenital lens malformations.