Freshwater shrimp opsin gene, protein encoded by same and application
A technology of gene encoding and opsin, applied in the fields of application, genetic engineering, plant gene improvement, etc., can solve the problem that opsin gene silencing expression has not been reported yet, and achieve the effect of reducing the expression of vitellogenin gene
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Embodiment 1
[0017] The acquisition of the full-length cDNA of embodiment 1 freshwater shrimp opsin gene
[0018] Total RNA extraction: select 3-4 mature female shrimp, aseptically dissect and remove the eye tissue, clip the eye stalk pigment in RNA preservation solution (TaKaRaBioInc.Japan), rinse and pre-treat, use TaKaRa Trizol kit Extract the total RNA of eye stalk of freshwater shrimp, and refer to the instruction manual of the kit for the specific operation steps.
[0019] The integrity of the total RNA was detected by 1.2% agarose gel electrophoresis, and the concentration and OD value of the extracted RNA were measured by a BioPhotometer ultraviolet spectrophotometer. Usually, the A260 / A280 was between 1.8 and 2.0, which met the experimental requirements.
[0020] First-strand cDNA synthesis: refer to the Takara M-MLV reverse transcription kit to synthesize the first-strand cDNA from the above total RNA.
[0021] Obtaining the full-length cDNA of the freshwater shrimp opsin gene: ...
Embodiment 2
[0031] The synthesis of embodiment 2 freshwater shrimp Opsin gene dsRNA
[0032] According to the nucleotide sequence of SEQ ID NO:1, use NCBI online dsRNA primer design software (http: / / www.flyrnai.org / cgi-bin / RNAi_find_primers.pl) to design and prepare double strands within the open reading frame of the nucleotide sequence RNA primers (SEQ ID NO: 3-SEQ ID NO: 4), using the total cDNA of freshwater shrimp as a template, performed in vitro transcription to synthesize dsRNA according to the instructions of the TranscriptAidTMT7 High Yield Transcription kit (Fermentas, Inc., USA). The prepared dsRNA was dissolved in DEPC water, its purity was detected on 1.5% agarose gel and its concentration was measured by a spectrophotometer. Female freshwater shrimps in the early stages of ovarian development (just after ovulation) were equally divided into two groups (experimental group and control group). The experimental group was injected with dsRNA solution at a dose of 4ug / g, and the c...
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