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Image of Simon Avery
Associate Professor and Reader, Faculty of Medicine & Health Sciences
BSc University of Dundee1988; PhD University of Dundee 1992; Research Associate, Dublin 1991-1992; Research Associate, Cardiff 1992-1994; Lecturer, Oxford Brookes University, 1994; Assistant Professor (1996), Adjunct Faculty (2000), Georgia State University; Lecturer (2000), Senior Lecturer (2004), Associate Professor and Reader (2006) University of Nottingham. Visiting Research Scholar, University of Adelaide, 1997; Member of Editorial Boards, Process Biochemistry (1997-1999), Microbiology (1998-2003), Applied and Environmental Microbiology (2000-2003), Fungal Biology Reviews (2007-); BMS Berkeley Award, 2004; EPSRC Peer-Review College (2003-2006); Council of the British Mycological Society (2004-2006); Vice-President of the British Mycological Society (2007-).
The interests of the Avery group lie in the effects of stress on cells, with a focus on environmental toxicants (e.g. metals and antimicrobials). We use the yeast Saccharomyces cerevisiae as a… read more
The interests of the Avery group lie in the effects of stress on cells, with a focus on environmental toxicants (e.g. metals and antimicrobials). We use the yeast Saccharomyces cerevisiae as a eukaryotic model to enable characterization of stress-effects at the whole-cell and molecular level. Current research projects in the Avery lab are focused on elucidating:
- The mechanism(s) of cellular metal toxicity, with emphasis on metal-induced oxidative stress
- The characterisation of variable phenotypes such as stress resistance between individual cells of genetically-uniform populations: phenotypic heterogeneity
- The elucidation of genes required for insusceptibility to pathogen-specific antibiotics and antimalarials (pharmacogenomics with yeast), and characterisation of novel modes of drug action
Principal experimental approaches include recombinant DNA techniques (cloning, PCR, mutagenesis), flow cytometry/cell sorting (FACS), DNA microarrays and other genome-wide screening methods, gene expression using the green fluorescent protein (GFP) reporter, protein analysis, purification and immunoblotting.
Variable expression of a GFP tagged EPA1 adhesin gene, between individual cells of the pathogenic yeast Candida glabrata .
Stop codon ( ade1-14 ) read-through during chromate stress in S.cerevisiae . Cr-induced mRNA mistranslation is a major mechanism of oxidative Cr toxicity (Holland et al., 2007).
University of Nottingham University Park Nottingham, NG7 2RD
telephone: +44 (0)115 9513300 (Undergraduate Enquiries) +44 (0)115 8230311 (Postgraduate Enquiries) fax: +44 (0)115 8230338 email: biology@nottingham.ac.uk
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