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Michael O'Connor, Ph.D.

Professor


Mailing Address:
University of Minnesota
Department of Genetics, Cell Biology, and Development
6-160 Jackson
321 Church St. SE
Minneapolis, MN 55455
USA


Education:
Ph.D. Tufts University, 1984

Honors:
Howard Hughes Medical Institute Senior Investigator
Office:
5-235J Moos Tower
P:612-626-0642
F: 612-625-5402

Email:
moconnor@umn.edu

Lab:
5-235 Moos Tower
P:612-625-8602
P:612-626-0636

Areas of Research Strength:

Molecular genetics of development
Growth factor signaling
Gene regulation

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Research Techniques:



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Research Interests:

The O'Connor laboratory is studying the function of several Drosophila
genes to learn how interacting cells differentiate to form spatial patterns.
One area of focus is to investigate how transcriptional regulation of the
bithorax complex is controlled. The genes of the bithorax complex are
responsible for specifying the identities of several segments of the fly.
The working model is that much of the DNA within the complex contains
large arrays of cis-acting control sequences that are organized into higher
order structures referred to as "regulatory domains". The lab is using molecular
and biochemical approaches to identify and purify the protein factors involved
in controlling the formation of these regulatory domains.

The lab's second area of interest is to learn how cells communicate with one
another during development. The particular group of signaling molecules that
are studied are members of the TGF-ß family of secreted polypeptides. These
effector molecules influence a wide variety of cellular processes including tissue
growth, differentiation and cell death. My lab is using genetic and molecular methods
to identify and clone genes that modulate the activity of these factors. The long term
objective is to identify and characterize additional components of TGF-ß signal
transduction systems so that we can understand the developmental functions
of these factors in the context of a complete biochemical pathway.

The third area of interest is to understand how steroid hormones regulate early
developmental processes. To this end the lab has identified a number of genes
that regulate biosynthesis of ecdysone the major molting hormone in all insects.
These genes are being characterized through genetic, molecular and biochemical
manipulations.

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Selected Publications:

Knox, S.,*, Ge* H., Ren, Y. Dimitroff, B.D., Howe, K.A.. Arsham, A.M., Easterday, M.C., Neufeld, T.P., O’Connor M.B., Selleck., S.B. (2007) Mechanisms of TSC-mediated Control of Synapse Assembly and Axon Guidance. Plos One in press

Rewitz K.F., O’Connor M.B., and Gilbert L.I.  Evolution of the insect Halloween family of cytochrome P450s: phylogeny, gene organization and functional conservation.  (2007) Insect  Biochem and Mol Bio. In press

Serpe, M. and O’Connor M.B. The metalloprotease Tolloid-related regulates Drosophila motoneuron axon guidance by activating latent TGF-ß type ligands. (2006)  Development 133: 4969-79

Takaesu, N.T., Huyman-Walsh, C.,  Ye, L., Wisotzkey, R.G., Stinchfield, M.J., O’Connor M.B., Wotton, D., and Newfeld, S.J.  dSno facilitates baboon signaling in the Drosophila brain by switching the affinity of Medea away from Mad towards dSmad2. (2006) Genetics, 174:1299-313

Umulis, D., Serpe, M. O’Connor, M.B.  and Othmer, H. (2006) Robust, bistable patterning of the dorsal surface of the Drosophila embryo. Proc. Nat. Acad. Sci. 103: 11613-8

Ono, H., Rewitz, K., Shinoda, T., Itoyama., K., Petryk, A., Rybczynski, R., Jarcho, M., Warren, J.T., Marqués,  G.M., Shimell, M., Gilbert, L.I., O’Connor, M.B. ( Oct. 2006) Spook and Spookier code for stage specific components of the ecdysone biosynthetic pathway in Diptera. Devel. Biol. 298: 555-70

Serpe M, Ralston A, Blair S, and O'Connor MB (2005) Matching cataltic activity to developmental function: Tlr processes Sog to help spcify the posterior crossvein in the Drosophila wing. Development 132: 2645-56.

Jadrick, J. L., O’Connor, M.B., and Coucouvanis, E. (2006) The TGF-ß activated kinase, TAK1, acts downstream of the TGF type I receptor, ALK1, to regulate vascular development in vivo. Development 133: 1529-41.

O’Connor, M.B., Umulis, D., Othmer, H., and Blair, S.S. (2006) Shaping BMP morphogen gradients in the Drosophila embryo and pupal wings. Development, 133: 183-93

Warren, J.T. Tank, L., Restifo L., Shimell, MJ., O'Connor, M.B., and Lawrence I. Gilbert. (2006) Discrete pulses of molting hormone, 20-hydroxyecdysone, during late larval development of Drosophila melanogaster: correlations with changes in gene activity. Developmental Dynamics 235: 315-26

Takaesu, N.T., Herbig, E.J., Zhitomersky, D., Johnson, A.N., O’Connor, M.B., and Newfeld S. J. (2005) DNA-binding domain mutations in SMAD genes yield dominant-negative proteins or a neomorphic protein that can activate WG target genes in Drosophila. Development, 132: 4882-94

Jorgenson, L.A., Sun, M., OConnor M.B., and Georgieff, M.K. (2005) Fetal Iron Deficiency Disrupts the Maturation of Synaptic Efficacy in Area CA1 of the Developing rat Hippocampus. Hippocampus, 15: 1094-102

Shimmi, O., Ralston, A., Blair, S., and O’Connor, M.B., (2005) Crossveinless codes for a new member of the Twisted gastrulation family required for producing peak levels of BMP signaling in the posterior crossvein of the Drosophila wing. Dev. Biol. 282: 70-83

Harumoto, T., Sakurai, K., Nakajima, M., Ueda, R., Saigo, K., O’Connor M.B., Nakato,H., Adachi-Yamada, T. (2005) Drosophila Spineless induces homeosis-dependent apoptotic and Hedgehog-mediated survival signals. Mol. Cell. Bio 25: 3140-50

Shimmi, O., Umulis, D., Othmer, H. and O’Connor M.B. (2005) Facilitated transport of a Dpp/Scw heterodimer by Sog/Tsg leads to robust patterning of the Drosophila blastoderm embryo. Cell, 120: 873-876

Parvy, J-P., Blais, C., Bernard F. , Warren J., Petryk A., Gilbert L.I., O'Connor
M.B and Dauphin-Villemant, C. (2005) A role for ßFTZ-F1 in regulating ecdysteroidtiters during post-embryonic development in Drosophila melanogaster. Dev. Biol 282: 84-94

Petryk, A., Shimmi, O. Tervonen, L., Jarcho, M., O’Connor M. B., and Gopalakrishnan, R., (2005) Twisted gastrulation inhibits differentiation and mineralization in MC3t3-E1 osteoblast-like cells. Bone 36: 617-26

Warren JT, Petryk A, Zhirtimersky D, Marques G, Parvy J-P, Dauphin-Vilemant C, O'Connor MB, and Gilbert LI (2004) Phantom is the Drosophila P450 enzyme that mediates the 25-hydroxylation of 2,22,25 deoxyecdysone to 2,22 deoxyecdysone. J. of Insect Biochem. and Mol. Bio. 34:991-101.

Johnson KG, Epstein E, Lincecum J, O'Connor MB and Van Vactor D (2004) The heparan sulfate proteoglycan Syndecan is required for midline guidance in the Drosophila central nervous system. Current Biology 14:499-504.

McCabe B, Hom S, Aberle H, Marques G, Haerry T, Wan H, MB O'Connor and CS Goodman and AP Haghighi (2004) Highwire regulates a presynaptic BMP signaling cascate essential fro synaptic growth. 241:891-905

Petryk A, Anderson RM, Jarcho MP, Leaf I, Carlson CS, Kingensmith J, Shawlot W, MB O'Connor (2004) The mammalian twisted gastrulation gene functions in foregut and craniofacial development. Development Biolgoy in 267:374-386.

Petryk A*, Warren JT*, Marques G, Jarcho MP, Parvy J-P, Dauphin-Vilemant C, Gilbert LI, and O'Connor MB (2003) Shade is the Drosophila P450 enzyme that mediates the hydroxylation of ecdysone to the steroid insect molting hormone 20-hydroxyecdysone. Proc Nat. Acad Sci. USA 100:13773-8.


Book Chapters:
Jadrich, J., O’Connor M.B. and Descotte, V., An Overview of TGF-ß signaling. In “Inborn Errors of Development”  2nd Edition (2007)  Ed.  Epstein, C. , Erickson R.P., and Wynshaw-Boris, A.  Oxford University Press  in press



To view these and other publications visit http://www.ncbi.nlm.nih.gov/PubMed
search menu should say PubMed
type O'Connor MB in the avaliable line

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Related Links:

http://www.gcd.med.umn.edu/OConnor

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