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The homeobox gene Pitx3 has been implicated as a key regulator for lens development because homozygous mutant aphakia mice, which are hypomorph for Pitx3, fail to develop lenses. One aim of my thesis is to investigate the underlying cellular and molecular mechanism of Pitx3 mediated lens defect by studying knockout mice lacking Pitx3. Chimeric embryos, generated by aggregating the wild type embryos with Pitx3 heterozygous or Pitx3 homozygous mutant ES cells, have been used to analyse lens development. Pitx3 null cells failed to colonise the lens epithelium in Pitx3 null wild type chimeric lens, suggesting that Pitx3 is cell-autonomously required for lens epithelial cells. Further study of Pitx3 null mice revealed an earlier downregulation of the lens epithelial markers PDGFR-alpha and E-cadherin in E11.5 lens epithelium, suggesting the loss of lens epithelial identity in Pitx3 deficient mice. Furthermore, cell cycle inhibitors p27KIP1 and p57KIP2 were ectopically expressed throughout the morphologically normal Pitx3 mutant lens vesicle, suggesting that inactivation of Pitx3 leads to cell cycle exit of epithelial lens cells. In addition, precocious activation of the fibre cell-specific proteins beta- and gamma-crystallins was observed in Pitx3 null lens. Beta-crystallin expression could be observed as early as E10.5 throughout the entire Pitx3 null lens vesicle and gamma-crystallin was detected in the malformed Pitx3 deficient lens at E11.5. RNA in situ hybridisation study revealed that the expression of the transcription factor Foxe3 was lost in Pitx3 null lens at E10.5, suggesting that Pitx3 maintains the lens epithelial cells partly via the regulation of transcription factor Foxe3 during lens development. Accordingly, this study provides the cellular and molecular basis for the lens defect observed in Pitx3 null and Pitx3 hypomorph aphakia mice. Pitx3 is a key transcription factor for the maintenance of lens epithelium and its absence leads to premature activation of fibre cell differentiation programme of lens epithelial cells. In the other part of my PhD, I have further developed the Pitx3-GFP knockin ES cell system with a goal to use this tool for the identification of determinants of midbrain dopaminergic (mDA) neurons, the type of cells lost in Parkinson’s disease (PD) patients. Experimental cell therapy and clinical trials have shown that foetal midbrain tissues, but not tissues from other DA neuron containing regions, can functionally restore the lost mDA neurons when transplanted in Parkinson’s disease patients. Therefore, it is essential to coax mDA properties on stem cell-derived neurons when considering therapeutic development. Within the central nervous system, Pitx3 is expressed exclusively in mDA neurons. Using a Pitx3-GFP knockin mouse line previously generated in the laboratory I have derived heterozygous and homozygous Pitx3-GFP ES cells from mouse blastocysts. In keeping with previous findings in our laboratory, the heterozygous Pitx3-GFP (Pitx3GFP/+) ES cell-derived GFP positive cells of neuronal morphology can be detected after in vitro differentiation using the PA6 coculture system. Furthermore, I have shown that these cells express tyrosine hydroxylase and midbrain markers Engrailed-1 and Nurr-1, demonstrating their midbrain characteristics. I have also generated supertransfectable Pitx3GFP/+ ES cells to offer a rapid and efficient way to express a transgene episomally. The Cre-mediated inducible system of Pitx3-GFP reporter ES cells has also been developed in our laboratory and I have shown that they have high induction efficiency thus allows transgene activation in a temporally controlled manner. The Pitx3 null ES cells showed impaired potential to differentiate into mDA neurons thus they may be used to evaluate candidate Pitx3 downstream target by gain-of-function test. In summary, I have developed a Pitx3-GFP reporter ES cell system to identify mDA regulators functionally by in vitro differentiation.

Thesis (M.S.)--West Virginia University, 2005. / Title from document title page. Document formatted into pages; contains viii, 99 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 82-99).

<p>There are 42 members of the homeodomain-leucine zipper (HDZip) family of transcription factors in <i>Arabidopsis thaliana</i>. This thesis focuses on the functional analysis of one member of this family, ATHB16, and on the biochemical properties of HDZip proteins. </p><p>To assess the function of the <i>ATHB16</i> gene, the expression of <i>ATHB16</i> was altered in transgenic Arabidopsis plants by using sense and antisense RNA constructs under the control of the 35S promoter. The reciprocal phenotypic effects associated with elevated and reduced levels of <i>ATHB16</i> expression suggested that, in wild-type plants, ATHB16 acts as a mediator of blue and red light effects on the regulation of plant growth and the timing of the floral transition. </p><p>In wild-type Arabidopsis, expression of <i>ATHB16</i> is high in leaves, intermediate in adult roots and inflorescences, and low in stems and siliques. The expression of <i>ATHB16</i> in the root is markedly increased in response to exogenous abscisic acid (ABA) treatment, but is reduced in the ABA response mutants <i>abil </i>and <i>abi2</i>, suggesting that <i>ATHB16</i> may be involved in ABA signal transduction. This hypothesis was corroborated by observations of alterations in sensitivity to ABA inhibition of root growth in seedlings of a T-DNA insertion mutant of <i>ATHB16</i> and of transgenic plants with elevated <i>ATHB16</i> levels. </p><p>HDZip proteins bind DNA as dimers. DNA-binding studies showed that different HDZip proteins interact with very similar target sequences <i>in vitro</i> and that they selectively form heterodimers with each other. For example, it was demonstrated that ATHB16 can heterodimerize with ATHB6 and ATHB7 in yeast and with ATHB5 <i>in vitro</i>, suggesting that ATHB16 may interact with other HDZip proteins in Arabidopsis. This interaction may have functional significance, since it may provide a mechanism for the plant to integrate different input signals, like light of different spectral qualities and water availability in the regulation of its growth. </p>

There are 42 members of the homeodomain-leucine zipper (HDZip) family of transcription factors in Arabidopsis thaliana. This thesis focuses on the functional analysis of one member of this family, ATHB16, and on the biochemical properties of HDZip proteins. To assess the function of the ATHB16 gene, the expression of ATHB16 was altered in transgenic Arabidopsis plants by using sense and antisense RNA constructs under the control of the 35S promoter. The reciprocal phenotypic effects associated with elevated and reduced levels of ATHB16 expression suggested that, in wild-type plants, ATHB16 acts as a mediator of blue and red light effects on the regulation of plant growth and the timing of the floral transition. In wild-type Arabidopsis, expression of ATHB16 is high in leaves, intermediate in adult roots and inflorescences, and low in stems and siliques. The expression of ATHB16 in the root is markedly increased in response to exogenous abscisic acid (ABA) treatment, but is reduced in the ABA response mutants abil and abi2, suggesting that ATHB16 may be involved in ABA signal transduction. This hypothesis was corroborated by observations of alterations in sensitivity to ABA inhibition of root growth in seedlings of a T-DNA insertion mutant of ATHB16 and of transgenic plants with elevated ATHB16 levels. HDZip proteins bind DNA as dimers. DNA-binding studies showed that different HDZip proteins interact with very similar target sequences in vitro and that they selectively form heterodimers with each other. For example, it was demonstrated that ATHB16 can heterodimerize with ATHB6 and ATHB7 in yeast and with ATHB5 in vitro, suggesting that ATHB16 may interact with other HDZip proteins in Arabidopsis. This interaction may have functional significance, since it may provide a mechanism for the plant to integrate different input signals, like light of different spectral qualities and water availability in the regulation of its growth.

During embryonic development a variety of tissues and organs such as the lung, eye, and kidney are being formed. The generation of functional organs is regulated by reciprocal cell-cell interactions. Via the secretion of soluble molecules one type of cells affect the fate of their neighboring cells. A central issue in organogenesis is how a cell interprets such extrinsic signals and adopts a specific fate, and how the cell in response to this signal establishes reciprocal signaling. Transcription factors play a critical role in this process and my thesis focuses on the role of the LIM-homeodomain transcription factor, Lhx2, in the development of three different organ systems, the liver, the hematopoietic system and the olfactory system. The liver is formed from endoderm of the ventral foregut and mesenchyme of the septum transversum (st) and its development depends upon signaling interactions between these two tissues. As the liver becomes a distinct organ it is colonized by hematopoietic cells and serves as hematopoietic organ until birth. The fetal liver provides a microenvironment that supports the expansion of the entire hematopoietic system (HS) including the hematopoietic stem cells (HSCs). Liver development in Lhx2-/- embryos is disrupted leading to a lethal anemia due to insufficient support of hematopoiesis. To further investigate the role of Lhx2 in liver development I analyzed gene expression from the Lhx2 locus during liver development in wild-type and Lhx2-/- mice. Lhx2 is expressed in the liver associated st mesenchymal cells that become integrated in the liver and contribute to a subpopulation of hepatic stellate cells in adult liver. Lhx2 is not required for the formation of these mesenchymal cells, suggesting that the phenotype in Lhx2-/- livers is due to the presence of defective mesenchymal cells. The putative role of Lhx2 in the expansion of the HS was examined by introducing Lhx2 cDNA into embryonic stem cells differentiated in vitro. This approach allowed for the generation of immortalized multipotent hematopoietic progenitor cell (HPC) lines that share many characteristics with normal HSCs. The Lhx2-dependent generation of HSC-like cell lines suggests that Lhx2 plays a role in the maintenance and/or expansion of the HS. To isolate genes putatively linked to Lhx2 function, genes differentially expressed in the HPC lines were isolated using a cDNA subtraction approach. This allowed for the identification of a few genes putatively linked to Lhx2 function, as well as several stem cell-specific genes. The antagonist of Wnt signalling, Dickkopf-1 (Dkk-1), was identified in the former group of genes as it showed a similar expression pattern in the fetal liver, as that of Lhx2 and expression of Dkk-1 in fetal liver and in HPC lines appeared to be regulated by Lhx2. This suggests that Dkk-1 plays a role in liver development and/or HSC physiology during embryonic development. During development of the olfactory epithelium (OE) neuronal progenitors differentiate into mature olfactory sensory neurons (OSNs) that are individually specified into over a thousand different subpopulations, each expressing a unique odorant receptor (OR) gene. The expression of Lhx2 in olfactory neurons suggested a potential role for Lhx2 in the development of OSNs. To address this OE from Lhx2-/- and wild-type mice was compared. In the absence of functional Lhx2 neuronal differentiation was arrested prior to onset of OR expression. Lhx2 is thus required for the development of OSN progenitors into functional, individually specified OSNs. Thus, Lhx2 trigger a variety of cellular responses in different organ systems that play important roles in organ development in vivo and stem cell expansion in vitro.

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