The aim of the research is to understand how cell-cell interactions regulate the formation of a critical cell type in the developing retina. Cell-cell interactions mediated by extracellular factors play a major role in the determination of cell type during development. They are the main factor in cell determination in both vertebrate and Drosophila retina. Drosophila can be studied by identifying genes through mutations that affect development, and characterizing how the genes function through developmental and molecular studies. Therefore the determination of R8 photoreceptor cells in Drosophila retina will be studied as a model to understand mechanisms of cell-cell interaction. In this system the behavior of individual calls can be studied, genetic techniques used"""""""" to identify and study gene products that are involved. R8 photoreceptor cells are the first cells to differentiate in the retina. The pattern of R8 photoreceptor cells is determined by a process involving lateral inhibition. Determination of cells in other parts of the Drosophila nervous system appears to be similar and requires some of the same genes. Lateral inhibition is also used to determine various cell types in other organisms. Two mutations known to affect the pattern of R8 photoreceptor cells are scabrous and Notch. scabrous encodes a putative secreted protein. Notch encodes a transmembrane protein. Notch is the Drosophila homologue of TAN-1 , a human proto-oncogene. scabrous and Notch also regulate cell determination in other parts of the Drosophila nervous system. To study cell-cell interactions in R8 photoreceptor determination, further important genes will be identified using a novel genetic screen based on properties of scabrous and Notch mutations. The roles of previously known genes will be investigated using scabrous expression as a sensitive assay for determination in their mutants. To test if Notch or other proteins is a receptor for scabrous, the nature of the scabrous protein products and Notch scabrous binding will be investigated biochemically.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM047892-02
Application #
3307300
Study Section
Genetics Study Section (GEN)
Project Start
1992-08-01
Project End
1997-07-31
Budget Start
1993-08-01
Budget End
1994-07-31
Support Year
2
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Baker, Nicholas E; Brown, Nadean L (2018) All in the family: proneural bHLH genes and neuronal diversity. Development 145:
Li, Ke; Baker, Nicholas E (2018) Regulation of the Drosophila ID protein Extra macrochaetae by proneural dimerization partners. Elife 7:
Wang, Lan-Hsin; Baker, Nicholas E (2018) Spatial regulation of expanded transcription in the Drosophila wing imaginal disc. PLoS One 13:e0201317
Baker, Nicholas E (2017) Patterning the eye: A role for the cell cycle? Dev Biol 430:263-265
Bhattacharya, Abhishek; Li, Ke; Quiquand, Manon et al. (2017) The Notch pathway regulates the Second Mitotic Wave cell cycle independently of bHLH proteins. Dev Biol 431:309-320
Wang, Lan-Hsin; Baker, Nicholas E (2015) Salvador-Warts-Hippo pathway in a developmental checkpoint monitoring helix-loop-helix proteins. Dev Cell 32:191-202
Wang, Lan-Hsin; Baker, Nicholas E (2015) E Proteins and ID Proteins: Helix-Loop-Helix Partners in Development and Disease. Dev Cell 35:269-80
Baker, Nicholas E; Li, Ke; Quiquand, Manon et al. (2014) Eye development. Methods 68:252-9
Baker, Nicholas E (2013) Developmental regulation of nucleolus size during Drosophila eye differentiation. PLoS One 8:e58266
Bhattacharya, Abhishek; Baker, Nicholas E (2012) The role of the bHLH protein hairy in morphogenetic furrow progression in the developing Drosophila eye. PLoS One 7:e47503

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