Personal tools

Stuart Peirson

Senior Research Scientist
My research interests centre around the photoreceptors and their photopigment proteins that mediate non-image forming responses to light. In particular, I have been investigating the signal transduction mechanisms which mediate responses to light in the retina, SCN and peripheral clocks.

Research Areas

Medical Sciences Division Themes

  • Neuroscience
  • Behavioural Science
  • Integrative Physiology
  • Genetics and Genomics
  • Bioinformatics and Statistics

Neuroscience Sub-Themes

Neuroscience Keywords

Techniques and Equipment

Collaborators

  • Russell Foster, Circadian and Visual Neuroscience
  • Mark Hankins, Circadian and Visual Neuroscience
  • Stephanie Halford, Circadian and Visual Neuroscience
  • Sumathi Sekaran, Circadian and Visual Neuroscience
  • Jeremy Taylor, Department of Physiology, Anatomy and Genetics
  • Matthew Wood, Department of Physiology, Anatomy and Genetics
Web Personal Website
Department Department of Ophthalmology
Stuart Peirson

The mammalian circadian axis

The rotation of the Earth provides a predictably changing environment in which all life has evolved. As a consequence, the ability to anticipate changes in environment confers an enormous selective advantage. To be able to anticipate such changes requires an internal means of telling the time – a circadian clock. The dramatic daily changes in both light quantity and spectral composition form the primary time cues for the circadian system, which detects light via the familiar rods and cones of the retina, as well as by other more unusual receptors, such as the pineal gland (in non-mammalian species) and the recently-identified photosensitive retinal ganglion cells (pRGCs). As well as circadian photoentrainment, pRGCs regulate a variety of acute non-image forming responses to light including melatonin suppression and the pupillary light response.

In mammals, these retinal photoreceptors project to a central clock located in the hypothalamic suprachiasmatic nuclei (SCN), which regulates activity and rest cycles. However, the circadian system consists of numerous independent clocks, in both the brain as well as peripheral tissues such as the heart, liver and kidney.

I am interested in a range of opsin-vitamin A based photopigments which mediate these non-image forming responses to light, using both molecular techniques such as qPCR, laser capture microdissection (LCM) and microarrays as well as behavioural techniques such as wheel-running assays and action spectroscopy.

A secondary field of research relates to technical aspects of quantitative real-time PCR (qPCR). I have applied this technique for a diverse range of biological studies, and am particularly interested in improving the speed, accuracy and reproducibility of qPCR methodologies. Much of this work has involved alternative approaches to data analysis, including the publication of a freely-available Excel-based platform, DART-PCR.

Sources of Funding

Biography

BSc in Neuroscience, University of Sheffield (1994-7) 

PhD in Neuroscience, Institute of Ophthalmology, University College London (1997-2001)

Research Associate, Imperial College London (2001-2006)

Senior Research Scientist, University of Oxford (2006-)

Selected Publications

Medical Sciences Office, John Radcliffe Hospital, Oxford, OX3 9DU - email : neuroscience@medsci.ox.ac.uk