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Appointments:
Professor
Department of Molecular Genetics
and Cell Biology
Committee on Cancer Biology
Committee on Deveopmental Biology
Committee on Genetics
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Education:
Ph.D., University of Washington
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Contact:
Phone: (773) 702-5694
Fax:
(773) 702-3172
E-Mail: rfehon@uchicago.edu
Address:
The University of Chicago
CLSC 925A
920 East 58th Street
Chicago, Illinois 60637
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Related Research Interests:
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Richard Fehon, Ph.D.
Regulation of Epithelial Polarity and Proliferation
During Development
Research Summary
Our interests center on the molecular mechanisms by
which signal transduction pathways are organized into specialized
membrane domains. In addition to their known role in organizing
receptors and downstream effectors into functional signaling ecmplexes,
such organized complexes function to integrate signaling activities
from multiple pathways and to segregate simultaneous but distinct
functions of a single pathway. We study this question in Drosophila
because of the utility of this system for studying the functions of
individual genes via mutagenesis, and for examing the functional
interactions between different genes that work together in a particular
cellular or developmental process.
Selected Papers
LaJeunesse DR, McCartney BM and Fehon RG. (2001). A
systematic screen for dominant second-site modifiers of Merlin/NF2
phenotypes reveals an interaction with blistered/DSRF and scribbler,
Genetics, vol. 158, pp. 667-679.
Ward, R.E., Schweizer, L., Lamb, R.S., and Fehon, R.G., (2001). The
FERM domain of Drosophila coracle, a cytoplasmic component of the
septate junction, provides functions essential for embryonic
development and imaginal cell proliferation, Genetics, vol. 159, pp.
219-228.
Tepass U, Tanentzapf G, Ward R and Fehon RG. (2001).
Epithelial cell polarity and cell junctions in Drosophila, Ann. Rev.
Genet., vol. 35, pp. 747-784.
Bretscher A, Edwards K and Fehon RG. (2002). ERM
proteins and Merlin: Integrators at the cell cortex, Nature Rev. Mol.
Cell Biol., vol. 3, pp. 747-784
Speck O, Hughes SC, Noren NK, Kulikauskas RM and Fehon
RG. (2003). Moesin functions antagonistically to the Rho pathway to
maintain epithelial integrity., Nature, vol. 421, pp. 83-87.
Genova JL and Fehon RG. (2003). Neuroglian, Gliotactin,
and the Na+/K+ ATPase are essential for septate junction function in
Drosophila, J. Cell Biol., vol. 161, pp. 979-989
Formstecher E, Aresta S, Collura V, Hamburger A, Meil A,
Trehin A,
Reverdy C, Betin V, Maire S, Brun C, Jacq B, Arpin M, Bellaiche Y,
Bellusci S, Benaroch P, Bornens M, Chanet R, Chavrier P, Delattre O,
Doye V, Fehon R, Faye G, Galli T, Girault JA, Goud B, de Gunzburg J,
Johannes L, Junier MP, Mirouse V, Mukherjee A, Papadopoulo D, Perez F,
Plessis A, Rosse C, Saule S, Stoppa-Lyonnet D, Vincent A, White M,
Legrain P, Wojcik J, Camonis J, Daviet L. (2005). Protein interaction
mapping:
a Drosophila case study. Genome Res. Mar;15(3):376-84. Epub 2005
Feb 14. (PubMed)
Li Q, Nance MR, Kulikauskas R, Nyberg K, Fehon R,
Karplus PA, Bretscher A, and Tesmer J. (2006). Self-masking in an
intact ERM-merlin protein: an active role for the central alpha-helical
domain. J. Mol. Biol. In press.
Hughes SC, and Fehon RG. (2006). Phosphorylation and activity of the
tumor-suppressor Merlin and the ERM protein Moesin are coordinately
regulated by the Slik kinase. J. Cell Biol. In press.
Cho E, Feng Y, Rauskolb C, Maitra S, Fehon R, Irvine KD. (2006).
Delineation of a Fat tumor suppressor pathway. Nat Genet. Sep 17; [Epub
ahead of print]
Fehon R. (2006). Cell biology: polarity bites. Nature. Aug
3;442(7102):519-20.
Maitra S, Kulikauskas RM, Gavilan H, Fehon RG. (2006). The tumor
suppressors Merlin and expanded function cooperatively to modulate
receptor endocytosis and signaling. Curr Biol. Apr 4;16(7):702-9.
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Faculty and Research
Programs
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