The Rel signal transduction pathway is of fundamental importance in biological processes as diverse as Drosophila development and vertebrate immunity. This project is designed to study the function of zygotic cact, and specifically test if zygotic dl is the biological target of zygotic cact or whether it regulates the function of some other Rel protein. The specific goals of this study are: (1) To determine the spatial and temporal pattern of expression of the zygotic cactus protein in the late embryo as well as during larval stages. To establish its function, we will ask whether the expression of cactus is tissue restricted or if it is ubiquitously expressed, and whether this expression is coincidental with that of dl. (2) To define the structural requirements essential for optimal cactus function. The maternal and zygotic cact proteins are very similar in structure and the maternal target of cact is known. Molecular analysis of zygotic alleles of cact, when compared with that of the maternal effect alleles will shed light on the mechanism of specificity of interaction with dorsal or another zygotic partner. (3) To define and analyze new components that interact with zygotic cactus. Histochemical, genetic and molecular methods will be used to address these question. The functional analysis of cactus in other stages of development and tissues of drosophila will provide information about, and access to, key biological processes regulated by similar signal transduction systems that use the inhibitory functions of the zygotic cact. Since Drosophila is genetically accessible, it serves as an excellent system for a thorough functional analysis of proteins in vivo. Our studies on cact structure governs its function will have a direct bearing on the two central issues of signal transduction: mechanism and specificity.

Project Start
Project End
Budget Start
Budget End
Support Year
12
Fiscal Year
1996
Total Cost
Indirect Cost
Das, Bidyut; Shi, Lingyan; Budansky, Yury et al. (2018) Alzheimer mouse brain tissue measured by time resolved fluorescence spectroscopy using single- and multi-photon excitation of label free native molecules. J Biophotonics 11:
Nicolas, Laura; Cols, Montserrat; Choi, Jee Eun et al. (2018) Generating and repairing genetically programmed DNA breaks during immunoglobulin class switch recombination. F1000Res 7:458
Juarez, Michelle T; Kenet, Chloe M (2018) Translating Research as an Approach to Enhance Science Engagement. Int J Environ Res Public Health 15:
Zheng, Simin; Kusnadi, Anthony; Choi, Jee Eun et al. (2018) NME proteins regulate class switch recombination. FEBS Lett :
Nicholl, Iain D; Matsui, Tsutomu; Weiss, Thomas M et al. (2018) ?-Catenin Structure and Nanoscale Dynamics in Solution and in Complex with F-Actin. Biophys J 115:642-654
Orlova, Natalia; Gerding, Matthew; Ivashkiv, Olha et al. (2017) The replication initiator of the cholera pathogen's second chromosome shows structural similarity to plasmid initiators. Nucleic Acids Res 45:3724-3737
Akula, Hari K; Kokatla, Hariprasad; Andrei, Graciela et al. (2017) Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products. Org Biomol Chem 15:1130-1139
Khalil, Reem; Levitt, Jonathan B (2017) Use of Synaptic Zinc Histochemistry to Reveal Different Regions and Laminae in the Developing and Adult Brain. J Vis Exp :
Shi, Lingyan; Lindwasser, Lukas; Wang, Wubao et al. (2017) Propagation of Gaussian and Laguerre-Gaussian vortex beams through mouse brain tissue. J Biophotonics 10:1756-1760
Shi, Lingyan; Lu, Luyao; Harvey, George et al. (2017) Label-Free Fluorescence Spectroscopy for Detecting Key Biomolecules in Brain Tissue from a Mouse Model of Alzheimer's Disease. Sci Rep 7:2599

Showing the most recent 10 out of 298 publications