There have been rapid advances in our understanding of pattern formation in Drosophila. A number of developmental genes encode regulators that interact in a cascade of transcriptional regulation in which genes are expressed in patterns of ever increasing detail. These localized regulators control the subsequent development of morphological pattern. This proposal is motivated by the premise that an increased understanding of the regulators involved and the sites at which they act will help define the mechanisms and circuitry of this pattern-forming cascade. We have focused on homeodomain regulators because these operate at many points in the cascade, and because the extraordinary evolutionary conservation of this domain suggests that this class of regulators is universally important. In a general approach to identify and characterize functional domains in these regulators, we will use in vitro mutagenesis to create variants of engrailed and fushi tarazu and will assay function at three levels - DNA binding activity and specificity will be assayed in vitro, transcriptional regulation will be tested by transient transfection of tissue culture cells, and functional integration in the cascade of pattern formation will be examined by P-element transformation of flies. In addition to this broad screen for new functional domains, we will conduct a more directed mutational dissection of homeodomain sequences and the DNA target sequences to which they bind based on our current knowledge of the DNA binding. This analysis will assess the degree to which these homologous regulators distinguish the target sites at which they act, reveal the biochemical basis of this discrimination, and examine the importance of site discrimination to the individual roles of these regulators in the embryo. Because of the rapid progress of our knowledge of the genetic control of early pattern formation in Drosophila our biochemical dissections can be integrated in a biological perspective of growing detail.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM037193-04
Application #
3292334
Study Section
Molecular Biology Study Section (MBY)
Project Start
1986-07-01
Project End
1994-06-30
Budget Start
1989-07-01
Budget End
1990-06-30
Support Year
4
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Yuan, Kai; Seller, Charles A; Shermoen, Antony W et al. (2016) Timing the Drosophila Mid-Blastula Transition: A Cell Cycle-Centered View. Trends Genet 32:496-507
Yuan, Kai; O'Farrell, Patrick H (2016) TALE-light imaging reveals maternally guided, H3K9me2/3-independent emergence of functional heterochromatin in Drosophila embryos. Genes Dev 30:579-93
Yuan, Kai; O'Farrell, Patrick H (2015) Cyclin B3 is a mitotic cyclin that promotes the metaphase-anaphase transition. Curr Biol 25:811-816
O'Farrell, Patrick H (2015) Growing an Embryo from a Single Cell: A Hurdle in Animal Life. Cold Spring Harb Perspect Biol 7:
Farrell, Jeffrey A; O'Farrell, Patrick H (2014) From egg to gastrula: how the cell cycle is remodeled during the Drosophila mid-blastula transition. Annu Rev Genet 48:269-94
Yuan, Kai; Shermoen, Antony W; O'Farrell, Patrick H (2014) Illuminating DNA replication during Drosophila development using TALE-lights. Curr Biol 24:R144-5
Farrell, Jeffrey A; O'Farrell, Patrick H (2013) Mechanism and regulation of Cdc25/Twine protein destruction in embryonic cell-cycle remodeling. Curr Biol 23:118-26
El Amine, Nour; Kechad, Amel; Jananji, Silvana et al. (2013) Opposing actions of septins and Sticky on Anillin promote the transition from contractile to midbody ring. J Cell Biol 203:487-504
Kechad, Amel; Jananji, Silvana; Ruella, Yvonne et al. (2012) Anillin acts as a bifunctional linker coordinating midbody ring biogenesis during cytokinesis. Curr Biol 22:197-203
Yuan, Kai; Farrell, Jeffrey A; O'Farrell, Patrick H (2012) Different cyclin types collaborate to reverse the S-phase checkpoint and permit prompt mitosis. J Cell Biol 198:973-80

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