Use this URL to cite or link to this record in EThOS:
Title: Transcriptional regulation of the platelet-derived growth factor alpha receptor (PDGFRA) gene during development
Author: Flores-Garcia, Lisbeth
ISNI:       0000 0004 2672 914X
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2007
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
The platelet-derived growth factor receptor (alpha subunit, pdgfra) is essential for the development of several types of precursor cells and their differentiated progeny for example, the cranial neural crest cells (CNCC), mesenchyme derived-cells (MSdC) and oligodendrocyte progenitors (OLPs) in the central nervous system. Previous studies suggested that separate c/s-acting specific regulatory elements (SREs) are required to drive pdgfra expression in different types of progenitor cells during development. As a first step towards understanding the control of pdgfra transcriptional regulation I set out to identify and characterize SREs in vivo. I analyzed 16 human PDGFRA-YAC/BAC mice transgenic lines, most of which I generated myself, and compared their PDGFRA expression patterns with each other and with previously-generated PDGFRA transgenics during development. These new transgenes gave me a better understanding of PDGFRA transcriptional regulation and allowed me to further refine the locations of many important SREs of this gene. Most of the SREs controlling expression in CNCC, sclerotome progenitors, MSdC, and first and second branchial arches seem to be located in the 3 kb upstream sequence of the PDGFRA gene. In addition, the postnatal OLP (pOLP)-SREs appear to lie in a region up to 63 kb downstream of the coding sequence. Furthermore, I used bioinformatic analysis to search for evolutionarily conserved sequences (CS) in the non-coding genomic sequence of the human PDGFRA gene, and found that the 3'-untranslated region has CSs, some of which might be pOLP-SREs because they are present in chicken, Xenopus and mammals but not zebrafish, in keeping with the observation that OLPs in all tetrapods examined - but not fish - express pdgfra in their OLPs. Overall, my results suggest a 'temporal colinearity' model of SREs for transcriptional activation of the pdgfra gene during development and that its expression might be managed by separate embryonic and postnatal regulatory systems.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available