<p>The Wingless (Wg)/Wnt signal transduction pathway directs a variety of cell fate decisions in developing animal embryos. Despite the identification of many Wg pathway components to date, it is still not clear how these proteins work together to generate cellular identities. We have carried out a series of genetic screens in Drosophila to identify new components involved in Wg signaling. Two mutant lines that modify wg-mediated epidermal patterning carry mutations in the RacGap50C gene. These mutations on their own cause cuticle pattern disruptions that include replacement of ventral denticles with naked cuticle, which indicate that the Wg pathway is ectopically activated in mutant embryos. In addition, RacGap50C mutations also interact genetically with naked cuticle and Axin, known negative regulators of the Wg pathway. These phenotypes suggest that the RacGap50C gene product participates in the negative regulation of Wg pathway activity. </p><p>In addition to the role of RacGap50C in regulating Wg signaling, RacGap50C, with the kinesin like protein Pavarotti (Pav), is essential for cytokinesis in dividing cells. Surprisingly, Pav, like RacGap50C is able to repress Wnt stimulated reporter gene activity in mammalian tissue culture. Expression of RacGap50C or Pav does not alter the levels of endogenous BetaCatenin, nor does it prevent BetaCatenin from entering the nucleus and binding the transcription factor TCF. However, reporter gene activity is significantly diminished in cells expressing RacGap50C or Pav, indicating an inability of this nuclear BetaCatenin to activate transcription. RacGap50C and Pav are also found in the nucleus of interphase cells and this subcellular localization may be relevant to their role in regulation of the Wnt pathway. Although RacGap50C and Pav colocalize, our data indicate distinct roles for these two proteins in Wnt signaling, as they show different genetic interactions with nkd in Drosophila embryos and with TCF in mammalian cells. </p><p>In addition, I have identified regions of the RacGap50C proteins that are dispensable for Wnt signaling repression. Pav-binding region, and the cysteine rich region of RacGap50C are not required for the activity of RacGap50C in Drosophila embryos, nor is GAP activity. Conversely, the middle region of the RacGap50C, which contains a nuclear localization signal, and the RacGap domain, which contains regions required for cofactor binding, are required for RacGap50C regulation of Wnt signaling. In summary, these results indicate a unique role for RacGap50C and Pav in regulating Wnt signaling at the level of BetaCatenin target gene activation.</p> / Dissertation
| Identifer | oai:union.ndltd.org:DUKE/oai:dukespace.lib.duke.edu:10161/668 |
| Date | 28 March 2008 |
| Creators | Jones, Whitney McRae |
| Contributors | Bejsovec, Amy M |
| Source Sets | Duke University |
| Language | en_US |
| Detected Language | English |
| Type | Dissertation |
| Format | 11815990 bytes, application/pdf |
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