WO2018170624A1 - Méthode de réduction des expressions de mir-185 et de mir-424 - Google Patents
Méthode de réduction des expressions de mir-185 et de mir-424 Download PDFInfo
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- WO2018170624A1 WO2018170624A1 PCT/CN2017/077174 CN2017077174W WO2018170624A1 WO 2018170624 A1 WO2018170624 A1 WO 2018170624A1 CN 2017077174 W CN2017077174 W CN 2017077174W WO 2018170624 A1 WO2018170624 A1 WO 2018170624A1
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- 230000014509 gene expression Effects 0.000 title claims abstract description 30
- 108091030938 miR-424 stem-loop Proteins 0.000 title claims abstract description 27
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- 238000000034 method Methods 0.000 title claims abstract description 15
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Definitions
- the present invention relates to the field of life sciences, and more particularly to a method of reducing the expression of microRNA-185 and microRNA-424.
- MicroRNA-185 (miR-185) is a 22 nt miRNA located in human chromosome 22ql l.
- DNMT1 methylation-related tumor suppressor miRNA that can be directly targeted.
- the expression of DNMT1 affects the methylation level of the whole genome, which in turn regulates the methylation status of certain genes, affecting gene expression; microRNA
- miR-424 (miR-424) is a miRNA discovered in recent years, which affects the biological effects and development of tumor cells by acting on target genes in various tumors, thereby affecting the biological effects and development of tumor cells.
- miR-424 is a multifunctional miRNA, which is associated with cell invasion and metastasis of cervical cancer, pancreatic cancer, etc.; it is associated with the expression of inflammatory factors such as IL-6 and TNF- ⁇ ; since the miR-424 promoter region has CpG islands It is also associated with methylation-induced gene silencing.
- miRNA silencing is the presentation of artificially synthesized oligonucleotide small molecules into cells, and endogenous miRNAs.
- a heteroduplex allows the miRNA to reduce the inhibition of the target gene to achieve regulation of gene function.
- Silencing of miRNAs is currently difficult to achieve.
- Commonly used methods for silencing miRNA mainly include anti-miR, antagomiR, miRNA sponge, etc. These methods have short effects such as short inter-turn, poor stability, complex construction, high requirements on instrument conditions, and complicated technical operations, which are difficult to achieve, simple, and effective. The effect of miR-185 and miR-424 expression was reduced.
- the object of the present invention is to provide a method for reducing the expression of miR-185 and miR-424, which is simple in design, easy to operate, and can easily and effectively down-regulate the expression of miR-185 and miR-424, Overcoming the deficiencies of the prior art.
- a method for the present invention a method for down-regulating expression of miR-185 and miR-424, and constructing eukaryotic expression targeting miR-185 and miR-424 on a eukaryotic vector pRI-GFP/Neo containing a HI promoter Vector pRI-185-424, which regulates the expression of miR-185 and miR-424 in eukaryotic cells; after transfecting the vector into eukaryotic cells in vitro, the expression of miR-185 and miR-424 was detected by real-time PCR Level.
- the sequences of pRI-GFP/Neo and Tud-185-424 were double-digested with Xho I and Bgl II, and the recovered fragments were purified and ligated overnight at 4 ° C. After ligation, single colonies were picked and inoculated. In LB medium containing l (Vg/ml kanamycin, 12 hours later, the bacterial solution was extracted and sent to Shanghai Yingjun for sequencing. The correctly sequenced vector was the successfully constructed recombinant plasmid pRI-185-424.
- the present invention utilizes a molecular biology technique to construct a eukaryotic expression vector containing Tud-185-424 based on a eukaryotic vector containing a CMV promoter, thereby down-regulating the expression of miR-185 and miR-424; After the vector was transfected into eukaryotic cells in vitro, the expression of miR-185 and miR-424 was detected by a real-time PCR instrument.
- the invention is not only suitable for transfection of cells, but also for the production of whole horizontal transgenic animals.
- FIG. 1 is a schematic diagram showing the structure of the pRI-GFP/Neo vector
- FIG. 2 is a quantitative PCR method for detecting the expression level of miRNA, wherein a. miR-185 expression, b. miR-424 expression.
- Tud RNA targeting hsa-miR-185 and hsa-miR-424 was designed according to the design principle of Tough Decoy RNA (Tud RNA).
- Tud RNA Tough Decoy RNA
- Tud-185-424 The enzyme was digested to obtain the desired Tud-185-424 sequence.
- the nucleotide sequence of Tud-185-424 is shown as SE Q ID No 1.
- 16HBE cells were seeded in a 6-well plate at a density of 30,000/ml, and 10
- Plasmid pRI-185-424 was transfected with Lipofectamine 2000 and continuously cultured at 5% CO 2 at 37 ° C. After 48 sputum, total RNA was extracted from each group, using Realtime.
- miR-185 and miR-424 were detected by PCR, and the results showed that the expression levels of m iR-185 and miR-424 were significantly down-regulated in the pRI-185-424 transfection group (Fig. 2), suggesting that the vector can be used for The expression of miR-185 and miR-424 was reduced.
- the present invention utilizes a molecular biology technique to construct a eukaryotic expression vector containing Tud-185-424 based on a eukaryotic vector containing a CMV promoter, thereby down-regulating the expression of miR-185 and miR-424; After the vector was transfected into eukaryotic cells in vitro, the expression of miR-185 and miR-424 was detected by a real-time PCR instrument.
- the invention is not only suitable for transfection of cells, but also for the production of whole horizontal transgenic animals.
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Abstract
L'invention concerne une méthode de réduction des expressions de miR-185 et de miR-424. La méthode comprend la construction d'un vecteur d'expression eucaryote pRI-185-424 ciblant miR-185 et miR-424 sur un vecteur eucaryote pRI-GFP/Neo qui contient un promoteur H1, régulant ainsi négativement les expressions de miR-185 et de miR-424.
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PCT/CN2017/077174 WO2018170624A1 (fr) | 2017-03-18 | 2017-03-18 | Méthode de réduction des expressions de mir-185 et de mir-424 |
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PCT/CN2017/077174 WO2018170624A1 (fr) | 2017-03-18 | 2017-03-18 | Méthode de réduction des expressions de mir-185 et de mir-424 |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101368213A (zh) * | 2008-10-13 | 2009-02-18 | 南京大学 | 血清微小核糖核酸试剂盒及其在乙肝早期诊断中的应用 |
CN101755208A (zh) * | 2007-07-25 | 2010-06-23 | 路易斯维尔大学研究基金会公司 | 作为诊断标记物的外来体相关微rna |
WO2010138263A2 (fr) * | 2009-05-28 | 2010-12-02 | University Of Massachusetts | Nouveaux virus adéno-associés (aav) et leurs utilisations |
CN102218144A (zh) * | 2010-04-13 | 2011-10-19 | 江苏命码生物科技有限公司 | 一种调节生物体内微小核糖核酸含量的方法及其用途 |
CN103920164A (zh) * | 2014-05-05 | 2014-07-16 | 山东大学 | MiR-424-5p在抑制转移性肝癌中的应用 |
-
2017
- 2017-03-18 WO PCT/CN2017/077174 patent/WO2018170624A1/fr active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101755208A (zh) * | 2007-07-25 | 2010-06-23 | 路易斯维尔大学研究基金会公司 | 作为诊断标记物的外来体相关微rna |
CN101368213A (zh) * | 2008-10-13 | 2009-02-18 | 南京大学 | 血清微小核糖核酸试剂盒及其在乙肝早期诊断中的应用 |
WO2010138263A2 (fr) * | 2009-05-28 | 2010-12-02 | University Of Massachusetts | Nouveaux virus adéno-associés (aav) et leurs utilisations |
CN102218144A (zh) * | 2010-04-13 | 2011-10-19 | 江苏命码生物科技有限公司 | 一种调节生物体内微小核糖核酸含量的方法及其用途 |
CN103920164A (zh) * | 2014-05-05 | 2014-07-16 | 山东大学 | MiR-424-5p在抑制转移性肝癌中的应用 |
Non-Patent Citations (1)
Title |
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XING-HUA LIAO ET AL.: "Human Cytomegalovirus Immediate Early Protein 2 Enhances Myocardin-mediated Survival of Rat Aortic Smooth Muscle Cells", VIRUS RESEARCH, vol. 192, 23 August 2014 (2014-08-23), pages 85 - 91, XP029071011, ISSN: 1872-7492 * |
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