Research Summary

Neuronal specification during nervous system development and maturation in Drosophila

Complex nervous system function depends upon the generation of many different subtypes of neurons and the lifelong modulation of their function by intercellular communication. The identity and function of a particular neuronal subtype is a product of the unique repertoire of ‘terminal differentiation’ genes that it expresses (eg. guidance molecules, ion channels, receptors, neurotransmitter biosynthetic enzymes, neuropeptides etc).

These genes are turned on after the neuron is born, but how neurons turn on the right set of genes is still poorly understood. Two regulatory inputs have been shown to play a role in regulating the expression of such ‘terminal differentiation’ genes; 1) the unique code of transcription factors expressed within the neuron, and 2) factors/signals that are secreted from the target cell that the neuron innervates. Our studies in Drosophila have demonstrated that these two inputs may actually functionally intersect to determine the mature gene expression repertoire of neurons.

Our research aims to investigate the mechanisms by which neurons selectively express the genes that define their unique identities and functions, exploring the roles of combinations of transcription factors and extrinsic signals. The genes and mechanisms that govern cell specification are highly conserved from invertebrates to humans. Therefore, we can learn much about the fundamental principles and molecular mechanisms relevant to vertebrate neuronal differentiation using the simpler nervous system and genetic amenability of Drosophila.

Disruption of transcription factors has been linked to congenital neurological disorders, and disruption of intercellular communication and trafficking of target-derived signals has been implicated in neurodegenerative disorders. Our studies will provide a mechanistic understanding of how these factors control gene expression pertinent to neuronal function, advancing our understanding of the aetiology of neurological disorders.

Resources

Our laboratory is situated in the Life Sciences Institute on the UBC Main Campus. Together with Dr. Shernaz Bamji, we run The Facility for Synaptic Imaging which consists of upright and inverted Olympus FV1000 laser scanning confocal microscopes. We also share a dedicated, fully-equipped Drosophila Facility with other fly labs in the building.

Technologies & Methods
Bio

Postdoc: Children’s Hospital Boston, & Harvard Medical School (2004-05); Harvard Medical School (2000-04)
PhD: University of Alberta (1994-2000)
MSc: Aberdeen University, Scotland (1992-93)
BSc (Hon): Aberdeen University (1988-1992)

Awards

Tula Foundation Investigator (Brain Research Centre)
CIHR New Investigator
MSFHR Scholar
EJLB Scholar

Publications

 
Comprehensive List
Google Scholar

Selected Publications

  1. Eade, KT and Allan, DW (2009) Neuronal phenotype in the mature nervous system is maintained by target-derived BMP signaling. Journal of Neuroscience 29:3852-3864.
  2. Allan, DW (2008) Combinatorial Codes in Neuronal Specification. The Encyclopedia of Neuroscience. Springer Press. Binder, M.D.; Hirokawa, N.; Windhorst, U.; Hirsch, M.C. (Eds.) In press Review.
  3. Allan DW, Park D, St. Pierre SE, Taghert PH, Thor S (2005) Regulators acting independently and in combinatorial codes to specify different aspects of neuronal identity. Neuron: 45 689-700.
  4. Miguel-Aliaga I, Allan DW, Thor S (2004) Independent roles of the dachshund and eyes absent genes in the specification of neuropeptidergic cell identity. Development 131(23); 5837-5848.
  5. Allan DW, Pierre SE, Miguel-Aliaga I, Thor S (2003) Specification of neuropeptide cell identity by the integration of retrograde BMP signaling and a combinatorial transcription factor code. Cell;113(1):73-86.
  6. Allan DW and Thor S (2003) Together at last. bHLH and LIM-HD regulators cooperate to specify motor neurons. Neuron. 2003 Jun 5;38(5):675-7.
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