Harvard University - Department of Molecular & Cellular Biology

CATHERINE DULAC

Dulac
Higgins Professor of Molecular and Cellular Biology
Howard Hughes Medical Institute Investigator

Email: dulac@fas.harvard.edu
Phone: 617-495-7893

Mail: BL 4017
The Biological Labs
16 Divinity Ave
Cambridge, MA  02138

Members of the Dulac Lab
List of Publications from PubMed

Courses

MCB 141. Molecular and Cellular Biology of the Senses and their Disorders
Catalog Number: 5205  View Course Website
Term: Spring Term 2014-2015.
Instructor: Catherine Dulac
Course Level: For Undergraduates and Graduates
Description: "The great art of life is sensation, to feel that we exist, even in pain." Lord Byron. Molecular basis of normal and pathological sensory perception, formation and modulation of sensory circuits during development and in the adult brain. Topics will include the mechanisms of sensory detection and discrimination, the discovery of key genes, cellular pathways and neural circuits affected in human disorders, molecular and genetic strategies for restoring normal sensation, coding of sensory information by the brain, establishment of appropriate connections in the developing brain, epigenetic influences on sensory function. Molecular, genetic and epigenetic approaches to normal and pathological sensing and associated behavior will be discussed.
Prerequisite(s): Prerequisite: LS 1a and LS 1b. Recommended: MCB 80 and a cell or molecular biology course such as MCB 60, MCB 52 or MCB 54, or MCB 115.
Meetings: Tu., Th., 1:30-3
MCB 344. Molecular and Developmental Neurobiology
Catalog Number: 2292  View Course Website
Term: Fall Term And Spring Term 2014-2015.
Instructor: Catherine Dulac
Course Level: Exclusively for Graduates
(View all MCB Courses)

Research

Our group is using molecular, genetic and electrophysiological techniques to explore the molecular and neuronal basis of innate social behaviors in the mouse. Two major lines of research are currently being pursued in the laboratory:

We are pursuing several projects at the molecular, cellular and systems levels in order to investigate the architecture and functional logic of neuronal circuits underlying pheromone signaling. The key questions we are addressing are: What is the nature of the mammalian pheromones and of the receptors that detect them? How are pheromone signals processed in the brain in order to generate species- and sex-specific behaviors such as aggression, mating, parental behavior, defensive behavior? What are the basic developmental processes that ensure appropriate neuronal connections between the olfactory sensory neurons and the brain? What are the respective roles of sensory experience and genetic information in setting appropriate pheromone-induced behaviors, and how are circuits underlying sex-specific behaviors established in the male and female brains?

The second set of projects explores the phenomenon of genomic imprinting in the brain, and the role of this mode of epigenetic modification in brain development and adult brain function. Genomic imprinting results in preferential expression of the paternally, or the maternally inherited allele of certain genes. We have recently used a genome-wide approach to characterize the repertoire of imprinted genes in the mouse embryonic and adult CNS. Our study uncovered over 1000 new loci with imprinted features, suggesting that imprinting is a major mode of epigenetic regulation in the brain. Imprinting appears to preferentially affect neural systems associated with social, motivational and homeostatic brain functions. Comparison of the imprinted gene repertoire in the adult hypothalamus and cortex, and in the developing brain demonstrates a complex spatiotemporal, species-, sex- and isoform-specific regulation. Genomic imprinting thus emerges as a major and dynamic mode of epigenetic regulation of brain function, with direct implications for the understanding of evolution and diseases. Future projects in the lab will aim at better understanding this mode of epigenetic regulation in mechanistic and functional terms.

Publications

Wu, Z., Autry, A.E., Bergan, J.F., Watabe-Uchida, M. and Dulac, C. (2014) Galanin neurons in the medial preoptic area govern parental behavior. Nature 509:325-330.

Bergan, J.F., Ben-Shaul, Y. and Dulac, C. (2014) Sex-specific processing of social cues in the medial amygdala. eLife 2014;3:e02743.

Chalfin, L., Dayan, M., Levy, D.R., Austad, S.N., Miller, R.A., Iraqi, F.A., Dulac, C. and Kimchi, T. (2014) Mapping ecologically relevant social behaviours by gene knockout in wild mice. Nat Commun. 5:4569.

Dulac, C., O’Connell, and L.A.Wu, Z., (2014) Neural Circuits Underlying Parental Behavior. Science 345:765-70.

Santoro, S.W. and Dulac, C. (2012) The activity-dependent histone variant H2BE modulates the life span of olfactory neurons. elife 2012;1:e00070. doi: 10.7554/eLife.00070. Epub 2012 Dec 13

Isogai, Y., Si, S., Pont-Lezica, L., Tan, T., Kapoor, V., Murthy, V.N., Dulac, C. (2011) Molecular organization of vomeronasal chemoreception. Nature 478:241-5

Dani, A., Huang, B., Bergan, J., Dulac, C.* and Zhuang, X.* (2010) Super-resolution Imaging of Chemical Synapses in the Brain. Neuron 68: 843-56 *Corresponding authors

Gregg, C., Zhang, J., Weissbourd, B., Luo, S., Schroth, G.P., Haig, D. and Dulac, C. (2010) High Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain. Science, 329: 643- 648

Gregg, C., Zhang, J., Butler, J.E., Haig, D. and Dulac, C. (2010) Sex-Specific Parent-of-Origin Allelic expression in the Mouse Brain. Science, 329: 682- 685

Dulac, C. (2010) Brain function and chromatin plasticity. Nature 465:728-735

Ben-Shaul, Y., Katz, L.C., Mooney R.M., & Dulac, C. (2010) In-vivo Vomeronasal Stimulation reveals Sensory Encoding of Conspecific and Allospecific Cues by the Mouse Accessory Olfactory Bulb. PNAS 107:5172-5177.

updated: 05/26/2015