@article {987,
	title = {Activation of the Sarcophaga lectin gene promoter in transgenic Drosophila},
	volume = {50},
	year = {Submitted},
	note = {08-10-200906-02-2012NormalDepartment of Cell Biochemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo, Bunkyo-ku, Tokyo, Japan.enghttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve\&db=pubmed\&dopt=Abstract\&list_uids=12111973},
	pages = {131 - 138},
	publisher = {Copyright 2002 Wiley-Liss, Inc.},
	abstract = {We established transgenic Drosophila strains in which the lacZ gene was expressed under the control of the 5{\textquoteright}-upstream regulatory region of the Sarcophaga lectin gene promoter (3.1 kbp). The reporter gene was expressed in the fat bodies of the transgenic larvae when they were immunized by body pricking or treatment with Escherichia coli, which was the same as the Sarcophaga lectin gene expression in Sarcophaga larvae. However, the same reporter gene was found to be expressed constitutively in the digestive tracts of the transgenic larvae even without immunization.},
	keywords = {*Depsipeptides, *Insect Proteins, *Lectins, C-Type, *Peptides, *Promoter Regions, Genetic, *Transcriptional Activation, Animals, Animals, Genetically Modified, Anti-Bacterial Agents/immunology, beta-Galactosidase/genetics, Cell Line, Diptera/genetics/*metabolism, Drosophila melanogaster/genetics/immunology, Escherichia coli/immunology, Genes, Reporter, Lectins/*genetics, Staphylococcus aureus/immunology, Tissue Distribution, Transgenes},
	author = {Tanji, T. and Kobayashi, A. and Natori, S.}
}
