Structure function analysis of the deubiquitylating enzyme Fam

Date

2006

Authors

Khut, Poon-Yu

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Wood, Stephen Andrew

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Abstract

The ubiquitin pathway is a highly conserved post-translational modification system best characterised for its roles in protein degradation and intracellular trafficking and is involved in a diverse spectrum of cellular processes. Ubiquitylation is opposed by deubiquitylating enzymes (Dubs), and the ubiquitin specific peptidase (USP) class of Dubs remove ubiquitin from specific substrates, thereby affecting protein fate. USPs exhibit broad sequence diversity except over their catalytic cores and it has been suggested that this sequence variation constitutes their individual substrate-specific binding sites. Fat Facets in Mouse (Fam) is a developmentally regulated USP whose function is crucial for mouse pre-implantation development. Fam is expressed in a complex fashion throughout development in a number of diverse tissue types and time points, well beyond its critical role in the early embryo. Fam's orthologue in fly, Fat Facets (faf) is also developmentally regulated and is required for both drosophila eye and syncytial stage development. Given the strengths of the zebrafish system as a developmental tool, the zebrafish orthologue of Fam, usp9 was identified and found to be highly conserved. Analysis of its expression pattern found considerable overlap with the published mouse patterns. Given the similarities between the mouse and zebrafish systems, a series of cross-species experiments were conducted to determine whether exogenous expression of highly conserved regions of FAM, could cause dominant-negative phenotypes in developing zebrafish embryos. Outside of the catalytic core, FAM's large N and C-terminal extensions consist of novel sequence bearing no similarity to any known domain. To delineate FAM domains, fulllength FAM was expressed in insect cells and subjected to partial proteolysis. Combining this data with recent structural predictions and computer analyses of the FAM sequence, four FAM domains were characterised with the first domain containing three possible subdomains. The predominant helical nature of the N and C-terminal extensions of FAM were predicted to form scaffolding structures, well suited to protein binding.

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School of Molecular and Biomedical Science

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Thesis (M.Sc.)-- University of Adelaide, School of Molecular and Biomedical Science, 2006.

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This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals

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