Preparation method of ddx27 gene deleted zebra fish mutant

A ddx27f1, gene deletion technology, applied in the field of obtaining ddx27 gene deletion zebrafish mutants, can solve the problem of less description of properties and specific functions

Active Publication Date: 2018-11-06
SHANGHAI OCEAN UNIV
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AI Technical Summary

Problems solved by technology

The DExD / H-box family plays an important role in almost all cellular processes involving RNA, such as gene transcription, pre-mRNA splicing, mRNA export, ribosome production, translation initiation, organelle gene expression, RNA degradation, etc., affecting RNA production and RNA polymorphisms, but the properties and specific functions of these enzymes in vivo are still seldom described

Method used

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  • Preparation method of ddx27 gene deleted zebra fish mutant
  • Preparation method of ddx27 gene deleted zebra fish mutant
  • Preparation method of ddx27 gene deleted zebra fish mutant

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Experimental program
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Embodiment

[0058] 1 Materials and equipment

[0059] 1.1 Experimental fish

[0060] The zebrafish used in this experiment were all AB strains, which were purchased from the Zebrafish Platform of the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences.

[0061] 1.2 Plasmid

[0062] The pUC19-gRNAscaffold plasmid is derived from the literature: Chang N, Sun C, Gao L, Zhu D, Xu X, ZhuX, Xiong JW, Xi JJ. Genome editing with RNA-guided Cas9nuclease in zebrafishembryos, Cell Res, 2013, 23(4) :465-472.

[0063] The pUC19-gRNAscaffold plasmid template sequence used in gRNA product synthesis is:

[0064] GTTTTAGAGCTAGAAATAGCAAGTTAAAATAAGGCTAGTCCGTTATCAACTTGAAAAAGTGGCACCGAGTCGGTGCTTTTTTT (SEQ ID NO. 7).

[0065] 1.3 Main reagents

[0066] DNAClean&Contentrator-5 (ZYMO RESEARCH, D4004), common DNA purification kit (TIANGEN, DP204-03), T7in vitro Transcription Kit (Ambion, AM1314), ethanol (absolute ethanol) (Sinopharm Chemical ...

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Abstract

The invention discloses a preparation method of a ddx27 gene deleted zebra fish mutant. The method comprises steps as follows: the target with a ddx27 gene knocked out is located on the sixth exon ofa ddx27 gene of zebra fish, and a gRNA sequence is designed; Puc19--gRNA scaffold plasmid is used as a template, and primers T7-ddx27-sfd and tracr rev are used for PCR amplification; gRNA is obtainedthrough purification and in-vitro transcription of a PCR product; gRNA and Cas9 protein are imported into the zebra fish, culture is performed, and a stably inherited ddx27gene mutant is obtained. Besides, the invention also discloses a phenotype of the ddx27 gene deleted zebra fish mutant, which plays an important role in research of biological function of the mutant.

Description

technical field [0001] The invention belongs to the field of molecular biology, and in particular relates to a specific method for obtaining ddx27 gene-deficient zebrafish mutants by using CRISPR / Cas9 gene editing technology. Background technique [0002] The CRISPR / Cas system belongs to the adaptive immune defense mechanism of bacteria and archaea. It is produced during the continuous evolution of organisms to protect its own genome from the interference of foreign nucleic acids. In 1987, researchers at Osaka University discovered clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-related genes (CRISPR- associated genes, Cas gene). CRISPR RNA (crRNA) guides the Cas protein in the form of base complementation to recognize the invading foreign genome and cut its DNA. According to the sequence and structure of the Cas protein, the CRISPR / Cas system can be divided into type I, type II and type III. Type I and II CRISPR-Cas systems can degrade exog...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/90C12N15/113A01K67/027
CPCA01K67/0276C12N15/113C12N15/902C07K14/47C12N2310/20A01K2227/40A01K2217/075A01K2267/0331C07K14/461C12N15/1137C12Y306/04013C12N9/90A01K2207/15A01K2217/056A01K2267/03
Inventor 张庆华时灿岳倩文祖尧李伟明
Owner SHANGHAI OCEAN UNIV
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