Function-based small molecular weight compound screening system in drosophila melanogaster
AssigneeThe Genetics Company, Inc.
InventorErnst Hafen
Life of this patent
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Abstract
A methodology for screening libraries of compounds for desirable biological/therapeutic activities, preferably using an automated system for the microinjection of compound(s) of interest into the open circulatory system (i.e., hemolymph) of Drosophila larvae genetically modified to sensitize a particular signaling pathway related to a human disease either by expression of a human disease gene or by the activation of a Drosophila gene that in the adult fly results in the development of an easily detectable phenotypes such that compounds that selectively interfere with this specific signaling pathway will modify or suppress the phenotype and can be identified rapidly and efficiently.
Claims26
A method of screening for a non-mutagenic compound, said method comprising:
- (a) providing at least one larva from a Drosophila so, wherein said Drosophila strain is characterized by a genetic modification affecting at least one detectable phenotype of at least one adult structure derived from an i f disk, wherein said phenotype is modified by the number of functional copies of at least one gene present in said larva, such that altered levels of the protein expressed by the functional copy of the gene in the larva affects said phenotype;
- (b) microinjecting at least one candidate non-mutagenic compound, alone or in combination, into the open circulatory system (hemolymph) of at least one genetically modified Drosophila larva;
- (c) allowing said microinjected Drosophila larva to undergo pupation to develop into an adult organism comprising the adult structure formed from the imaginal disk and
- (d) analyzing the phenotype of at least one adult structure of the treated Drosophila larva and compare said phenotype to that in at least one untreated larva;
- wherein a difference in the visible phenolpic effect between the treated and untreated Drosophila indicates that the non-mutagenic compound modulates activity of at least one protein involved in establishing the adult sure.
The method of claim 17, wherein said genetic modification of Drosophila is comprised of modification of one or more gene(s) selected from the group comprising:
- a Raf gene;
- a Ras proto-oncogene system or pathway;
- a WNT tumor suppressor system or pathway;, a hedgehog development regulator (HH) system or pathway;
- a sonic hedgehog development regulator (SHH) system or pathway;
- a retinoblastoma tumor suppressor (Rb) system or pathway;
- an activated Drosophila protein kinase B (PKB/AKT) gene;
- an activated human PKB/AKT gene;
- an activated insulin receptor gene;
- an insulin receptor substrates (IRS) gene or pathway;
- c-src proto-oncogene or pathway;
- c-Jun proto-oncogene or pathway;
- c-myc proto-oncogene or pathway, p53;
- Janus kinases (JAK/STAT pathway);
- nitric oxide (NO);
- calmodulin;
- cAMP dependent protein We (PKA) or pathway;
- Ca2+ dependent protein kinase (PKC) or pathway, growth factors such as GH, TGF, PDGF and the like;
- receptor tyrosine kinases (RTKs) and pathways;
- interferons (IFN) or pathways;
- lipid metabolites or pathway;
- steroid hormones or pathway, phosphatidylinositol or pathway;
- G-protein coupled receptors or pathways;
- c-abl proto-oncogene or pathway;
- TGF-β and Smad gene family members;
- interleukins or pathway;
- GTPases or pathway;
- and ionophores or pathway.
A method of screening for a non-mutagenic compound, said method comprising:
- (a) providing at least one larva from a Drosophila strain, wherein said Drosophila strain is characterized by a genetic modification affecting at least one undetectable phenotype of at least one adult structure derived from an imaginal disk wherein said phenotype is modified by the number of functional copies of at least one gene present i said larva, such that altered levels of the protein expressed by the functional copy of the gene in the larva affects said phenotype;
- (b) microinjecting at least one candidate non-mutagenic compound, alone or in combination, into the open circulatory system (hemolymph) of at least one genetically modified Drosophila larva;
- (c) allowing said microinjected Drosophila larva to undergo pupation to develop into an adult organism comprising the adult structure formed from the imaginal disk;
- and
- (d) analyzing the phenotype of at least one adult structure of the treated Drosophila larva and comparing said phenotype to that in at least one untreated larva;
- wherein a difference in the visible phenotypic effect between the treated and untreated Drosophila indicates that the non-mutagenic compound modulates activity of at least one protein involved in establishing the adult structure.
Dependencies are inferred from the claim text.