The long-term goal of this research is to understand in molecular detail how cells choose to form a particular organ and how they carry out this decision. The Principal Investigator proposes to address these questions by a systematic analysis of formation of a simple tissue, the salivary glands, in a genetically-tractable organism, the fruit fly, Drosophila melanogaster. In the past several years, the Principal Investigator has identified the factors that control where salivary glands will form and the number of cells committed to a salivary gland fate. In the next few years, the proposed studies will provide information on how these factors work in combination to control expression of salivary gland genes. The Principal Investigator also has perhaps the largest single collection of genes expressed in a specific tissue. Her goal is to pinpoint and characterize the genes that function very early in salivary gland development, particularly genes that coordinate the major morphogenetic movements required to internalize the salivary glands and to form functional epithelial tubes. To achieve these goals, four specific aims are proposed.
In Aim 1, studies are proposed to test if activation of three early salivary gland genes by the transcription factors SCR, EXD and HTH is direct and, if so, will learn how TSH, ABD-B and DPP-signaling block activation.
In Aim 2, studies are proposed to address the role of two early transcription factors, FKH and HKB, in salivary gland internalization. Fkh mutants fail to complete internalization of the salivary gland and show extensive salivary cell death. Hkb mutants initiate internalization at the wrong place and form abnormally shaped salivary glands.
In Aim 3, studies are proposed to address the role of two genes, rib and D-SemaII, in positioning the salivary gland. Rib mutants have defects in directed migration of salivary gland cells and in D-SemaII mutants the distal portion of the salivary gland is abnormally positioned.
In Aim 4, studies are proposed to find new genes required for salivary gland morphogenesis. These new genes will be identified both from the Principal Investigator's collection of genes known to be expressed in the developing salivary gland and from an EMS saturation screen. The proposed studies will provide a working blueprint for the early events of organ formation in all higher organisms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE013899-02
Application #
6497905
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Program Officer
Kousvelari, Eleni
Project Start
2001-02-01
Project End
2006-01-31
Budget Start
2002-02-01
Budget End
2003-01-31
Support Year
2
Fiscal Year
2002
Total Cost
$271,819
Indirect Cost
Name
Johns Hopkins University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Wells, Michael B; Villamor, Jordan; Andrew, Deborah J (2017) Salivary gland maturation and duct formation in the African malaria mosquito Anopheles gambiae. Sci Rep 7:601
Chung, SeYeon; Kim, Sangjoon; Andrew, Deborah J (2017) Uncoupling apical constriction from tissue invagination. Elife 6:
Manning, Lathiena; Sheth, Jinal; Bridges, Stacey et al. (2017) A hormonal cue promotes timely follicle cell migration by modulating transcription profiles. Mech Dev 148:56-68
Hanlon, Caitlin D; Andrew, Deborah J (2016) Drosophila FoxL1 non-autonomously coordinates organ placement during embryonic development. Dev Biol 419:273-284
Fox, Rebecca M; Andrew, Deborah J (2015) Changes in organelle position and epithelial architecture associated with loss of CrebA. Biol Open 4:317-30
Wells, Michael B; Andrew, Deborah J (2015) ""Salivary gland cellular architecture in the Asian malaria vector mosquito Anopheles stephensi"". Parasit Vectors 8:617
Hanlon, Caitlin D; Andrew, Deborah J (2015) Outside-in signaling--a brief review of GPCR signaling with a focus on the Drosophila GPCR family. J Cell Sci 128:3533-42
Fox, Rebecca M; Andrew, Deborah J (2015) Transcriptional regulation of secretory capacity by bZip transcription factors. Front Biol (Beijing) 10:28-51
Andrew, Deborah J; Yelon, Deborah (2015) Editorial overview: Developmental mechanisms, patterning and organogenesis. Curr Opin Genet Dev 32:v-viii
Chung, Seyeon; Andrew, Deborah J (2014) Cadherin 99C regulates apical expansion and cell rearrangement during epithelial tube elongation. Development 141:1950-60

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