Dorsal is a maternal regulatory factor that initiates dorsoventral patterning of the precellular Drosophila embryo. It is a member of the Rel family of transcription factors that is initially distributed throughout the cytoplasm of unfertilized eggs, but shortly after fertilization it translocates into nuclei. This nuclear transport process is regulated by the Toll signaling pathway, which is employed in a variety of processes, including insect immunity and acute/inflammatory responses in mammals. The resulting Dorsal nuclear gradient specifies the embryonic mesoderm, neurogenic ectoderm, and dorsal ectoderm, through the differential regulation of target genes such as snail, sog, and dpp. The snail gene encodes a zinc finger repressor that establishes the boundary between the presumptive mesoderm and neurogenic ectoderm. It is a short-range repressor that must bind within 100 bp of either upstream activators or the core promoter in order to inhibit gene expression. Dpp is a member of the TGF-beta family, and a Dpp activity gradient subdivides the dorsal ectoderm into the amnioserosa and dorsal epidermis. The Dpp gradient depends on sog, which encodes a secreted inhibitory protein that binds Dpp. High levels of Sog are thought to inhibit Dpp signaling, while low levels enhance signaling. The proposed study represents a continuation of our efforts to determine how the Toll-Dorsal signaling pathway controls the dorsoventral patterning of the early Drosophila embryo. The research plan includes three specific aims: (i) determine how Snail functions as a repressor; (ii) identify the components of the Toll signaling pathway that diffuse in precellular embryos to create the Dorsal nuclear gradient; and, (iii) determine how Sog- Dpp interactions create a peak Dpp signaling threshold that specifies the amnioserosa.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM046638-12
Application #
6386275
Study Section
Molecular Biology Study Section (MBY)
Program Officer
Greenberg, Judith H
Project Start
1991-07-01
Project End
2003-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
12
Fiscal Year
2001
Total Cost
$270,134
Indirect Cost
Name
University of California Berkeley
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Lim, Bomyi; Levine, Michael; Yamazaki, Yuji (2017) Transcriptional Pre-patterning of Drosophila Gastrulation. Curr Biol 27:286-290
Esposito, Emilia; Lim, Bomyi; Guessous, Ghita et al. (2016) Mitosis-associated repression in development. Genes Dev 30:1503-8
Fukaya, Takashi; Lim, Bomyi; Levine, Michael (2016) Enhancer Control of Transcriptional Bursting. Cell 166:358-368
Farley, Emma K; Olson, Katrina M; Zhang, Wei et al. (2015) Suboptimization of developmental enhancers. Science 350:325-8
Farley, Emma K; Olson, Katrina M; Levine, Michael S (2015) Regulatory Principles Governing Tissue Specificity of Developmental Enhancers. Cold Spring Harb Symp Quant Biol 80:27-32
Levine, Michael; Cattoglio, Claudia; Tjian, Robert (2014) Looping back to leap forward: transcription enters a new era. Cell 157:13-25
Levine, Michael (2014) The contraction of time and space in remote chromosomal interactions. Cell 158:243-244
Boettiger, Alistair Nicol; Levine, Michael (2013) Rapid transcription fosters coordinate snail expression in the Drosophila embryo. Cell Rep 3:8-15
Lagha, Mounia; Bothma, Jacques P; Esposito, Emilia et al. (2013) Paused Pol II coordinates tissue morphogenesis in the Drosophila embryo. Cell 153:976-87
Lagha, Mounia; Bothma, Jacques P; Levine, Michael (2012) Mechanisms of transcriptional precision in animal development. Trends Genet 28:409-16

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