The Role of ELf5 in Mouse Trophoblast Stem Cells

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dc.contributor.advisorMcLeay, Lance M.
dc.contributor.advisorPfeffer, Peter
dc.contributor.authorRedgate, Emma Louiseen_NZ
dc.date.accessioned2010-08-23T00:22:52Z
dc.date.available2010-08-23T00:22:52Z
dc.date.issued2010en_NZ
dc.description.abstractElf5 is a DNA transcription factor that has been identified as being involved in placentation of the early embryo. Elf5 is expressed in the extra embryonic ectoderm (ExE), a lineage that contributes to the placenta of the embryo. Pluripotent trophoblast stem (TS) cells can be derived from the ExE and can be cultured in vitro. Such cells can contribute to all the placental lineages when injected back into an embryo. Elf5 homozygous mutant embryos do not possess an ExE and trophoblast stem cells cannot be derived and the mutation is therefore embryonic lethal. When Elf5 is knocked out, the TS cells in the ExE are thought to differentiate into EPC/giant cells leading to the absence of the ExE. In previous experiments in this laboratory, potential Elf5 targets were identified by RNA interference in mouse trophoblast stem cells followed by global gene expression analysis using an Affymetrix array. In the present experiments these results have now been confirmed by siRNA induced knockdown of Elf5 in TS cells followed by quantitative real time PCR of potential target genes. Most of the target genes that were affected by Elf5 knockdown were changed in the same way by growth factor removal and therefore stem cell differentiation. This suggested that Elf5 usually acts to maintain the TS cells in a stem cell fate. As Elf5 is expressed in the ExE, whole mount In situ hybridisation was used to determine if the genes showed the correct spatial and temporal patterning to be in vivo relevant Elf5 targets. The targets that were down regulated upon Elf5 knockdown (and therefore positively regulated by Elf5) were expressed in the ExE as expected. Genes that were up-regulated upon Elf5 knockdown (and therefore usually repressed by Elf5) were expressed in the differentiated ectoplacental cone or giant cells. . Preliminary work was also carried out for the over-expression of Elf5 by a tamoxifen inducible Elf5. TS cells were stably transfected with a plasmid containing Elf5 fused to a tamoxifen inducible ERT2 receptor and a VP16 transcriptional activation domain to turn Elf5 into a potent activator, and were analysed for target gene expression. Preliminary data showed that Elf5 is involved in a complex transcriptional network of events as the genes did not behave as expected when Elf5 was turned into an activator. The effect of Elf5 knockdown on TS cells has been studied closely in terms of morphology, proliferation, changes in DNA content and apoptosis. The knockdown of Elf5 caused an increase in the number of differentiated cells (as shown by changes in morphology and DNA content). This further supported the knockdown and in situ data. There was no change in proliferation or apoptosis. These experiments which demonstrate which genes are regulated by Elf5 and the changes to TS cellular characteristics when Elf5 is knocked down, support the proposal that Elf5 acts as a trophoblast stem cell maintenance factor of the extraembryonic ectoderm of the mouse.en_NZ
dc.format.mimetypeapplication/pdf
dc.identifier.citationRedgate, E. L. (2010). The Role of ELf5 in Mouse Trophoblast Stem Cells (Thesis, Master of Science (MSc)). The University of Waikato, Hamilton, New Zealand. Retrieved from https://hdl.handle.net/10289/4392en
dc.identifier.urihttps://hdl.handle.net/10289/4392
dc.language.isoen
dc.publisherThe University of Waikatoen_NZ
dc.rightsAll items in Research Commons are provided for private study and research purposes and are protected by copyright with all rights reserved unless otherwise indicated.
dc.subjectTrophoblasten_NZ
dc.subjectTrophoblast stem cellsen_NZ
dc.subjectElf5en_NZ
dc.subjectplacentaen_NZ
dc.subjectExEen_NZ
dc.subjectgiant cellsen_NZ
dc.subjectsiRNAen_NZ
dc.titleThe Role of ELf5 in Mouse Trophoblast Stem Cellsen_NZ
dc.typeThesisen_NZ
pubs.place-of-publicationHamilton, New Zealanden_NZ
thesis.degree.disciplineBiological Sciencesen_NZ
thesis.degree.grantorUniversity of Waikatoen_NZ
thesis.degree.levelMasters
thesis.degree.nameMaster of Science (MSc)en_NZ
uow.date.accession2010-02-24en_NZ
uow.identifier.adthttp://adt.waikato.ac.nz/uploads/adt-uow20100224.182821
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