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Pluripotency transcription factor function during primordial germ cell development

Reference	BB/L002736/1
Principal Investigator / Supervisor	Professor Ian Chambers
Co-Investigators / Co-Supervisors	Mr Nicola Festuccia
Institution	University of Edinburgh
Department	Sch of Biological Sciences
Funding type	Research
Value (£)	461,408
Status	Completed
Type	Research Grant
Start date	31/03/2014
End date	31/07/2017
Duration	40 months

Abstract

Nanog is required for PGC development beyond the time of epigenetic reprogramming at E11.5, but little is known about how Nanog exerts this function. Here we propose to investigate the role of Nanog and its target gene Esrrb at this time in order to provide a more detailed understanding of the molecular changes occurring at this important biological transition. In this work we aim to determine 1 what structural features are required for Nanog protein to function in PGC development? 2 to what extent can Nanog function in PGC development be rescued by its target gene, Esrrb? 3 what are the target genes that function downstream of Nanog and Esrrb to facilitate PGC development? In aim 1, we will determine which domains of Nanog mediate function in PGCs. Nanog mutants will be knocked-in to the Nanog locus in Nanog-/- ES cells and in vitro differentiation used to test their ability to sustain PGC development. We have shown that Esrrb is the most upregulated Nanog target gene in ES cells and that Esrrb can compensate for Nanog in driving maintenance and acquisition of pluripotency. In aim 2 we will investigate the existence of a similar functional overlap during PGC development by crossing mice with an Esrrb knock-in at Nanog and mice with a conditional Nanog knock-out allele that is specifically deleted in PGCs to establish whether complete functional rescue by Esrrb occurs. To address aim 3, we will take advantage of the fact that deletion of the Nanog conditional knock-out allele leads to expression of GFP. Therefore, the transcriptional profiles of FACS purified GFP+ PGCs from Nanog+/CKO, Nanog-/CKO or NanogEsrrbKI/CKO embryos will be used to characterise the overlap in Nanog and Esrrb target genes during PGC development.

Summary

The aim of the proposed work is to study the factors regulating formation of functional germ cells, oocytes in females and sperm in males. We will focus on the role of Nanog, an important molecule involved at distinct stages during embryonic development. We will determine what parts of Nanog are required to mediate function in developing primordial germ cells (PGCs for short), the embryonic cells that will give rise to the adult germ cells. We will compare Nanog proteins from different species for their ability to function in mouse cells, since the mouse is the mammalian species where these processes are best understood. We will investigate whether Nanog function is unique, or whether other factors, such as Esrrb, can play a similar role in PGCs. We will determine how Nanog exerts its function in driving germ cell development by identifying the genes regulated by Nanog in this process. This study will delineate the mechanisms through which Nanog functions. We will learn if Nanog function has been conserved throughout evolution and which parts of the Nanog molecule are important. In a broader sense, since primordial germ cells and the cells of the early embryo that retain unrestricted differentiation potential are similar, we will understand better how the factors required for the formation of these distinct cells work. Understanding how functional germ cells are formed is of great importance for the progress of reproductive medicine. Learning how pluripotent cells are regulated has high impact on regenerative medicine strategies. The continued existence of a sexually reproducing species requires effective formation of germ cells that possess a haploid DNA complement and that can join with another germ cell of the opposite sex during fertilisation to form a new individual. PGC development from cells set aside early in development involves changes in gene expression and modifications of the chromatin, the complex of DNA and protein in which the genome is packed, as the PGCs migrate to the site where the genitals form, known as the genital ridges. Once the PGCs enter the genital ridges they undergo further changes to their chromatin that erase memories of their parental origin. This sets a blank slate onto which instructions for gene expression in the next generation can be written. These changes are directed by a number of important factors able to influence the expression of other genes, amongst which is Nanog. We have shown that Nanog is required for continued PGC development during the period of chromatin remodelling. Interestingly, Nanog is also required at the other developmental period in which profound chromatin remodelling occurs; the formation of cells with unrestricted differentiation potential (pluripotency) in the pre-implantation embryo. Pluripotency can be conveniently studied in cells grown in culture and derived from pre-implantation embryos: embryonic stem (ES) cells. Nanog controls the ability of ES cells to indefinitely duplicate. Our recent work has characterized the genes acting downstream of Nanog in ES cells. We consistently found that the gene most up-regulated by Nanog induction was Esrrb. We further showed that Esrrb could recapitulate many of the functional properties previously ascribed to Nanog and, importantly could do this in the absence of Nanog. A further key finding is that, in ES cells lacking Esrrb, the ability of Nanog to sustain pluripotency is compromised. This demonstrates unequivocally that Esrrb is a critical downstream mediator of Nanog function in ES cells. We now propose to investigate in greater detail the importance of Nanog function in germ cell development and determine whether a similar functional relationship exists between Nanog and Esrrb in PGCs. Our study has the potential to highlight new similarities between the pluripotent cells of the pre-implantation embryo and PGCs, ultimately improving our understanding of the principles governing both cell populations.

Impact Summary

The social beneficiaries of the proposed research are to be found within the wider public. The general public will benefit from the results of the proposed work mainly in three ways: 1) The proposed research has potential medical implications in two fields of broad interest: reproductive medicine and regenerative medicine. Reproductive medicine: the potential contribution of the outlined experiments to the understanding of the molecular control of germ cell specification can not be directly translated in advances of clinical relevance. Nonetheless, delineating the steps and mechanisms of germ cell specification is of pivotal importance in understanding the process of gamete production, and correcting potential defects observed in this lineage. Regenerative Medicine: The proposed work has the potential to enhance the current understanding of the principles governing the specification of pluripotent cell populations. Since the ability to promote reprogramming to pluripotency of differentiated cells from patients is a key step in most cellular replacement therapies, the direct investigation of the principles and factors governing this process is of immediate relevance to the field. 2) The biological research carried out during the proposed project will contribute towards maintaining the high standard of academic excellence currently enjoyed by the Centre for Regenerative Medicine. This will be reflected in the ability of the Centre for Regenerative Medicine and the University of Edinburgh being able to offer educational opportunities for undergraduate and post-graduate students training in our group. 3) The conceptual advances and tangible material, such as pictures, diagrams and illustrations generated to present the results of the proposed experiments will add to the resources used by our science communication staff during outreach activities aimed at raising awareness of the latest advances in the field of stem cell biology and regenerative medicine.

Committee	Research Committee C (Genes, development and STEM approaches to biology)
Research Topics	Stem Cells
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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