Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.642810
Title: Tex19 : a germ cell-specific gene associated with pluripotency
Author: Childs, A. J.
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2007
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Abstract:
Germ cells are the only population of cells in the adult organism shown to retain pluripotency – the ability to differentiate into all the different germ layers of the embryo. This property is shared with embryonic stem cells and tumour-derived embryonal carcinoma cells, and the molecular mechanisms underpinning pluripotency are likely to be similar in all three systems. The core circuitry of transcription factors required to establish and maintain pluripotency is relatively well characterised. However, many of these important transcription factors also regulate a large number of genes involved in processes other than transcription, some of which may also play an important role in maintaining stem cell plasticity. Understanding the entire molecular basis of pluripotency will improve the use of ES cells as a model system for differentiation and development, enhance the therapeutic potential of stem cells and provide insights into the mechanisms of tumourigenesis. Testis Expressed Gene 19 has been identified in screens for genes expressed in spermatogonia, embryonic stem cells, and for targets of translational regulation by the germ cell-specific protein Dazl. The work presented here characterises the expression pattern of Tex19 in the gonads and stem cells, establishing a correlation between the expression of Tex19 and pluripotent potentiality. A human homologue of Tex19 is found to be expressed in stem cells and cancer, and the evolution of the gene family in mammals is investigated. Finally, the function of Tex19 and its relationship with Dazl is also investigated.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.642810  DOI: Not available
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