Dataset GMR_Brain_exp_1
| General Information | |||
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| Name | GMR_Brain_exp_1 | Species | D. melanogaster |
| Dataset type | construct collection | FlyBase ID | FBlc0000201 |
| Source & Content | |||
| Consists of |
Fly stocks carrying GAL4 transgenic constructs designed to be expressed in adult brain.
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| Created by | |||
| Available from | |||
| Strain |
iso-1
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Stage & tissue | |
| Cell Line |
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Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Description & Members
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| Description |
Collection of stocks carrying GAL4 transgenes fused to defined putative enhancer fragments from selected D. melanogaster genes;
a targeted insertion site is used. The goal is to establish a collection of enhancers driving expression in small subsets
of cells in adult brain.
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| Component collection(s) |
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Experimental protocol
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| Vector | |||
| Sample preparation |
925 genes for which available expression data or predicted function implied expression in a subset of cells in the adult brain
were selected. Spanning the flanking upstream and downstream intergenic regions of these genes, as well as any of their introns
larger than 300 bp, regions were selected for testing that averaged 3 kb in length and overlapped (in regions that could not
be covered by a single fragment) by approximately 1 kb.
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| Collection preparation |
The fragment of genomic DNA to be tested for enhancer activity was generated by PCR, cloned into a Gateway donor vector, and
verified by DNA sequencing. Site-specific recombination was used to transfer the fragment into the integration vector pBPGUw or pBPGw. Constructs in pBPGUw use a Drosophila synthetic core promoter (DSCP). Constructs in pBPGw use the putative endogenous promoter of the selected gene. Constructs were inserted into the P{CaryP}attP2 target element by phiC31 site-specific integration.
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| Mode of assay |
Expression of GAL4 was detected either directly by in situ hybridization to the GAL4 mRNA or by assaying expression of a UAS-GFP
fusion gene.
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| Assay platform | |||
| Data analysis |
Eventual goal is to select lines directing expression in small subsets of cells (typically 10-200 cells) in the adult brain.
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Additional data
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Synonyms & Secondary IDs
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| Reported As | |||
| Symbol Synonym |
GMR_Brain_exp_1
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| Secondary FlyBase IDs | |||
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References
( 1 )
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| Research paper |
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Recent Updates
Description & Members