Vector for efficiently labeling zebra fish PGC, and preparation method and use of transgenic fish
A zebrafish, transgenic technology, applied in the direction of using vectors to introduce foreign genetic material, applications, fish farming, etc., can solve the problem of failing to construct transgenic lines and other issues
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Embodiment 1
[0056] Embodiment 1: A kind of preparation method of the transgenic fish of highly efficient labeling zebrafish primordial germ cells, its steps are:
[0057] 1. Preparation of transgenic lines based on the Gal4 / UAS system using mRFP to mark zebrafish primordial germ cells, see the strategy diagram figure 1 shown. Then design the primers needed to amplify each fragment in the transgenic vector. The primer sequences are shown in the table below:
[0058]
[0059]
[0060] 2. Construct the transgenic vector pTol2 (kop: KalTA4-UTRnos1, CMV: EGFP-S V40) of the activated strain Tg (kop: KalTA4).
[0061] (1) Construct the vector pMD-18T-UTRnos1.
[0062]Using the plasmid kop-new-F-EGFP-UTRnos1 as a template (Blaser, H., Eisenbeiss, S., Neumann, M., Reichman-Fried, M., Thisse, B., Thisse, C.and Raz, E .(2005) "Transition from non-motile be haviour to directed migration during early PGC development in zebrafish." J Cell Sci 118, 4027-4038), nos13'UTR-F and nos13'UTR-R we...
Embodiment 2
[0081] Embodiment 2: The application of a transgenic fish that efficiently marks zebrafish primordial germ cells in fish bioengineering, the process is:
[0082] 1. KalTA4mRNA is specifically expressed in primordial germ cells in embryos of activated strain Tg (kop:KalTA4).
[0083] (1) KalTA4 probe preparation.
[0084] A. Template preparation and purification.
[0085] Using plasmid pTol2 (kop: KalTA4-UTRnos1, CMV: EGFP-SV40) as template, Probe-KalTA4-F and T3-nos13'UTR-R (with T3 promoter sequence) as primers, PCR amplified template DNA, refer to Axygen's PCR clean up kit recovered the PCR products and used them as probes for synthetic probes.
[0086] B. Probe synthesis and recovery.
[0087]RNA probes were transcribed and synthesized according to Promega's T3 RNA polymerase instructions, and the probes were recovered according to the instructions of sigma spin post-reaction chean-up columns.
[0088] (2) In situ hybridization was used to detect the expression of KalTA...
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