Michael Gordon

Professor

I use molecular genetics, imaging, and behaviour to explore the organization, function, and development of neural circuits that process sensory information in the fruit fly brain.

Our brains are composed of billions of neurons, wired together in neural circuits that process information from the environment and produce behaviours. My lab is interested in the organization, function, and development of these circuits. We study this problem in the fruit fly Drosophila melanogaster, an organism with a brain that is much simpler than ours (~100,000 neurons compared to our ~100 billion), but still capable of generating complex behaviours. The fly also offers a powerful array of molecular and genetic tools for identifying, manipulating, and measuring the activity of neural circuits. With a focus on the circuits underlying taste perception and feeding behaviour, we are interested in the following questions:

  1. How are sensory circuits organized? We use behavioural assays to identify new circuit neurons, and imaging of specialized molecular labels to understand how these neurons are connected together in the brain.
  2. How do neural circuits control behaviour? We use genetic techniques to manipulate neuron activity and measure the behavioural consequences. We also use functional live imaging to measure neural activity in an awake, behaving fly.
  3. How do neural circuits adapt? We use molecular genetics to manipulate gene function and determine how different molecules modulate circuit activity and fly behaviour.
  4. How do circuits develop? We use a combination of genetics and behaviour to uncover molecules regulating circuit assembly and understand their roles during development.

Our hope is that answering these questions will reveal fundamental principles of neural circuit assembly and function, and important molecules that regulate feeding. Since many of the characteristics of fly circuits are likely to be conserved in mammals, this should give us insight into our own brain, and how it controls what (and how much) we eat.

Motor control in a Drosophila taste circuit
Neuron 61(3): 373-84
Gordon MD, Scott K
2009
Fly neurobiology: development and function of the brain
Embo Rep 9(3):239-42
Gordon MD, Manzo A, Scott K
2008
Pathogenesis of Listeria-infected Drosophila wntD mutants is associated with elevated levels of the novel immunity gene edin
PLoS Pathogens 4(7): e1000111
Gordon MD, Ayres JS, Schneider DS, Nusse R
2008
Drosophila eiger mutants are sensitive to extracellular pathogens
PLoS Pathogens 3(3): e41
Schneider DS, Ayers JS, Brandt SM, Costa A, Dionne MS, Gordon MD, Mayberry EM, Moule MG, Pham LN, Shirasu-Hiza MM
2007
Wnt signaling: multiple pathways, multiple receptors, and multiple transcription factors
J Biol Chem 281(32): 22429-33
Gordon MD and Nusse R
2006
WntD is a feedback inhibitor of Dorsal/NF-κB in Drosophila development and immunity
Nature 437(7059): 746-9
Gordon MD, Dionne MS, Schneider DS, Nusse R
2005
Genetic identification of effectors downstream of Neu (ErbB-2) autophosphorylation sites in a Drosophila model
Oncogene 22(13): 1916-26
Settle M, Gordon MD, Nadella M, Dankort D, Muller W, Jacobs JR
2003
Dynamic movements of organelles containing Niemann-Pick C1 protein: NPC1 involvement in late endocytic events
Mol Biol Cell 12(3):601-14
Ko DC, Gordon MD, Jin JY, Scott MP
2001
Genetic analysis of vein function in the Drosophila embryonic nervous system
Genome 43(3):564-73
Lanoue BR, Gordon MD, Battye R, Jacobs JR
2000
The UNC-119 family of neural proteins is functionally conserved between humans, Drosophila and C. elegans
J Neurogenet 13(4):191-212
Maduro MF, Gordon M, Jacobs R, Pilgrim DB
2000