Promoter for specifically expressing gene in poultry skeletal muscle and application
A promoter and skeletal muscle technology, applied in the direction of using vectors to introduce foreign genetic material, peptides, DNA/RNA fragments, etc., can solve the problem of not having the ability to target gene expression regulation, limiting the application of tissue-specific promoters, and specific initiation Problems such as the small number of children
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Embodiment 1
[0044] In the embodiment of the present invention, a fragment from 1000 bp upstream of the transcription initiation point of CARP to 203 bp downstream of the transcription initiation point is amplified by PCR method (i.e. -1000 to +203 bp, (-): indicates upstream of transcription initiation, (+): indicates Downstream of transcription initiation), Gene ID of CARP gene: 378926. This fragment was cloned into the luciferase reporter vector pGL3-basic (Promega). Using a series of primers with restriction sites, a series of vectors with 5' deletion structures were constructed by PCR. P-386(-1000~+203bp), P-386(-386~+203bp), P-355(-355~+203bp), P-337(-337~+203bp), P-319( -319~+203bp), P-286(-286~+203bp), P-269(-269~+203bp), P257(-257~+203bp), P227(-227~+203bp), P-189 (-189~+203bp), (-): indicates upstream of transcription initiation, (+): indicates downstream of transcription initiation, for example: P-337 (-337~+203bp) is upstream of the transcription initiation point linked to CA...
Embodiment 2
[0047] The vector of Example 1 was transfected into CFM, chicken fibroblasts and DT40 cells, and CFM, chicken fibroblasts and DT40 cells were cultured in DMEM containing 10% fetal bovine serum and 1% double antibody, and placed in Containing 5% carbon dioxide, 37°C incubator. Transfection experiments were performed with lip2000 (Invitrogen, USA) when the cell density reached 70%.
Embodiment 3
[0049] Carry out the luciferase reporter assay on the CFM, chicken fibroblasts and DT 40 cells that have been transfected in Example 2, the steps are as follows: inoculate CFM, chicken fibroblasts and DT 40 cells in a 12-well plate, transfect with Lip2000 After 24 h, the luciferase activity was detected with a luciferase reporter system (Promega, USA). All transfections were performed in triplicate, and firefly luciferase activity was normalized to kidney luciferase activity for each sample, and data are presented as mean ± standard deviation and included at least three separate experiments. Two independent samples were compared using t test. All analyzes were conducted with two-tailed test, and the difference was significant (Pfigure 1 as shown, figure 1 It can be seen that in CFM cells, the deletion of -1 kb to -373 base pairs (bp) has no significant effect on the activity of the CARP promoter. However, deletion of this region from -337bp to -227bp resulted in a significan...
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