The long term goal of the proposed research is to elucidate mechanisms that specify positional information and pattern development. Our focus is on the developmental compartments of Drosophila, specifically the role and function of the anterior/posterior (A/P) compartment borders. During the past granting periods, we identified several genes that are expressed in compartment-specific patterns, including hedgehog (hh) in all posterior compartment cells and cubitus interruptus (ci) in all anterior compartment cells, and we established that these patterns of expression are linked by an elegant regulatory relationship: engrailed (en), expressed only in posterior compartment cells, positively regulates hh and negatively regulates ci; Hh protein, secreted by posterior compartment cells positively regulates ci in anterior compartment cells. Through these actions, the asymmetry of en expression at the compartment border initiates a cascade of genetic responses that patterns both compartments and thus implicates the compartment boder as the key organizer. Specific objectives proposed to further elucidate this important regulatory pathway are: (1) To investigate the regulatory functions that are responsible for patterning en expression (2) To characterize the mechanism through which en regulates hh expression (3) To identify and characterize the receptor that mediates the hedgehog signal (4) To characterize the mechanism responsible for the compartment-specific expression of ci (5) To establish the identity of the active form of the Ci protein and to determine its enzymatic function.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM030637-18
Application #
2900558
Study Section
Genetics Study Section (GEN)
Project Start
1982-03-01
Project End
2001-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
18
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Biochemistry
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Chen, Weitao; Huang, Hai; Hatori, Ryo et al. (2017) Essential basal cytonemes take up Hedgehog in the Drosophila wing imaginal disc. Development 144:3134-3144
Kornberg, Thomas B (2017) Distributing signaling proteins in space and time: the province of cytonemes. Curr Opin Genet Dev 45:22-27
Kashima, Risa; Redmond, Patrick L; Ghatpande, Prajakta et al. (2017) Hyperactive locomotion in a Drosophila model is a functional readout for the synaptic abnormalities underlying fragile X syndrome. Sci Signal 10:
Kashima, Risa; Roy, Sougata; Ascano, Manuel et al. (2016) Augmented noncanonical BMP type II receptor signaling mediates the synaptic abnormality of fragile X syndrome. Sci Signal 9:ra58
Huang, Hai; Kornberg, Thomas B (2016) Cells must express components of the planar cell polarity system and extracellular matrix to support cytonemes. Elife 5:
Roy, Sougata; Kornberg, Thomas B (2015) Paracrine signaling mediated at cell-cell contacts. Bioessays 37:25-33
Yu, Dan; Baird, Michelle A; Allen, John R et al. (2015) A naturally monomeric infrared fluorescent protein for protein labeling in vivo. Nat Methods 12:763-5
Rao, Prashanth R; Lin, Li; Huang, Hai et al. (2015) Developmental compartments in the larval trachea of Drosophila. Elife 4:
Huang, Hai; Kornberg, Thomas B (2015) Myoblast cytonemes mediate Wg signaling from the wing imaginal disc and Delta-Notch signaling to the air sac primordium. Elife 4:e06114
Yu, Dan; Gustafson, William Clay; Han, Chun et al. (2014) An improved monomeric infrared fluorescent protein for neuronal and tumour brain imaging. Nat Commun 5:3626

Showing the most recent 10 out of 24 publications