ZFIN ID: ZDB-PUB-110629-33
MIP/Aquaporin 0 Represents a Direct Transcriptional Target of PITX3 in the Developing Lens
Sorokina, E.A., Muheisen, S., Mlodik, N., and Semina, E.V.
Date: 2011
Source: PLoS One   6(6): e21122 (Journal)
Registered Authors: Semina, Elena
Keywords: none
MeSH Terms:
  • Animals
  • Aquaporins/physiology*
  • Base Sequence
  • Cell Line
  • Chromatin Immunoprecipitation
  • DNA Primers
  • Electrophoretic Mobility Shift Assay
  • Eye Proteins/physiology*
  • Homeodomain Proteins/genetics*
  • Humans
  • In Situ Hybridization
  • Lens, Crystalline/embryology*
  • Mice
  • Promoter Regions, Genetic
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors/genetics*
  • Transcription, Genetic*
  • Zebrafish
PubMed: 21698120 Full text @ PLoS One
The PITX3 bicoid-type homeodomain transcription factor plays an important role in lens development in vertebrates. PITX3 deficiency results in a spectrum of phenotypes from isolated cataracts to microphthalmia in humans, and lens degeneration in mice and zebrafish. While identification of downstream targets of PITX3 is vital for understanding the mechanisms of normal ocular development and human disease, these targets remain largely unknown. To isolate genes that are directly regulated by PITX3, we performed a search for genomic sequences that contain evolutionarily conserved bicoid/PITX3 binding sites and are located in the proximity of known genes. Two bicoid sites that are conserved from zebrafish to human were identified within the human promoter of the major intrinsic protein of lens fiber, MIP/AQP0. MIP/AQP0 deficiency was previously shown to be associated with lens defects in humans and mice. We demonstrate by both chromatin immunoprecipitation and electrophoretic mobility shift assay that PITX3 binds to MIP/AQP0 promoter region in vivo and is able to interact with both bicoid sites in vitro. In addition, we show that wild-type PITX3 is able to activate the MIP/AQP0 promoter via interaction with the proximal bicoid site in cotransfection experiments and that the introduction of mutations disrupting binding to this site abolishes this activation. Furthermore, mutant forms of PITX3 fail to produce the same levels of transactivation as wild-type when cotransfected with the MIP/AQP0 reporter. Finally, knockdown of pitx3 in zebrafish affects formation of a DNA-protein complex associated with mip1 promoter sequences; and examination of expression in pitx3 morphant and control zebrafish revealed a delay in and reduction of mip1 expression in pitx3-deficient embryos. Therefore, our data suggest that PITX3 is involved in direct regulation of MIP/AQP0 expression and that the alteration of MIP/AQP0 expression is likely to contribute to the lens phenotype in cataract patients with PITX3 mutations.