Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

siRNA-IR sequence and application of male Macrobrachium rosenbergii sex transition

A technology of Macrobrachium rosenbergii and sequence, applied in DNA/RNA fragments, recombinant DNA technology, biochemical equipment and methods, etc., can solve the problems of expensive synthesis kits, high injection dose, long sequences, etc., and reduce the immune response of larvae. The effect of stimulating response, small injection dose, and improving survival rate

Active Publication Date: 2021-04-06
HUAZHONG AGRI UNIV
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although this method can interfere with and inhibit gene expression, the injection dose is relatively high, the required sequence is relatively long, and the synthesis kit is relatively expensive and the cost is high.
For the application to production practice, this method still has some cost factors

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • siRNA-IR sequence and application of male Macrobrachium rosenbergii sex transition
  • siRNA-IR sequence and application of male Macrobrachium rosenbergii sex transition
  • siRNA-IR sequence and application of male Macrobrachium rosenbergii sex transition

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Embodiment 1 can interfere and suppress the siRNA screening of IR gene

[0022] According to the sequence of Macrobrachium rosenbergii IR gene (accession number: FJ409645), an interference sequence called siRNA-IR was designed and synthesized; the device was designed using online siRNA design software (https: / / www.invivogen.com / sirnawizard / design.php) Select the siRNA-IR sequence (see Table 1). Exclude fragments containing SNP sites and non-open reading frames from the alternative siRNA-IR, and remove sequences with too high and too low GC content, and finally perform Blast analysis and discard non-specific binding sequences. After obtaining the ideal siRNA-IR sequence, four oligos were designed according to the requirements of the TaKaRa siRNA in vitro transcription synthesis kit, named oligo 1, oligo 2, oligo 3 and oligo 4 (see Table 1). These four oligo sequences were entrusted to Wuhan Qingke Biotechnology Co., Ltd. to synthesize them.

[0023] Table 1 Sequences o...

Embodiment 2

[0026] Example 2 Preparation of siRNA-IR double-stranded Oligo DNA

[0027] Dissolve the synthesized single-stranded Oligo DNA with sterilized distilled water to prepare a 100 pmol / μl DNA solution, and prepare the Oligo DNA annealing reaction solution according to the components in Table 2 and Table 3. The prepared Oligo DNA annealing reaction solution was placed in a PCR amplification instrument, treated at 95°C for 2 minutes, cooled to 25°C over 45 minutes, and then kept at 25°C for 10 minutes. This step enables a stack of single-stranded oligo DNA to be annealed to form double-stranded oligo DNA. Eventually two sets of Oligo DNA will be obtained and named OligoA and Oligo B.

[0028] Table 2 Annealing reaction solution of Oligo A

[0029] Reagent dose 10X Annealing Buffer 2μl 100 pmol / μl Oligo 1 2μl 100 pmol / μl Oligo 2 2μl RNase free dH 2 o

14μl

[0030] Table 3 Annealing reaction solution of Oligo B

[0031] Rea...

Embodiment 3

[0032] Example 3 siRNA-IR in vitro transcription

[0033] The Oligo A and Oligo B formed by the annealing reaction were used to prepare the RNA in vitro transcription reaction solution according to the components in Table 4, mixed evenly and then centrifuged slightly so that the transcription reaction solution was collected at the bottom of the EP tube. The prepared transcription reaction solution was placed in a PCR amplification instrument and reacted at 42°C for 4 hours. After 4 hours, the transcription reaction solution was taken out, and 2 μl of RNasefree DNase I (5 U / μl) and 1 μl of RNase T1 (5 U / μl) were added to the original reaction tube. After mixing slightly, put it into a PCR amplification instrument and react at 37°C for 2 hours. After in vitro transcription, siRNA-IR will be purified. Add 23 μl of water-saturated acidic phenol / chloroform / isopropanol (25:24:1) to the in vitro transcription reaction solution, mix it upside down and centrifuge at 10,000 rpm at 25°...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a siRNA-IR sequence of male Macrobrachium rosenbergii sex transition and its application; it uses siRNA interference technology to inhibit the expression of IR gene, promotes the sex transition of male Macrobrachium rosenbergii, and obtains pseudo-female shrimp; The IR gene fragment of Macrobrachium rosenbergii was screened and obtained from the transcriptome of Macrobrachium rosenbergii, and siRNA was designed and synthesized according to the IR gene sequence of Macrobrachium rosenbergii, named siRNA‑IR. Before the sex differentiation period, it was introduced into Macrobrachium rosenbergii by microinjection method, interfered and inhibited the expression of IR gene in Macrobrachium rosenbergii, and promoted the sex transition of Macrobrachium rosenbergii. Compared with dsRNA interference technology, siRNA interference technology has a smaller injection dose, can reduce costs, can effectively reduce the immune stress response of postlarvae of Macrobrachium rosenbergii, and improve the survival rate of pseudo female shrimp.

Description

technical field [0001] The invention relates to the field of sex transformation of Macrobrachium rosenbergii, in particular to an siRNA-IR sequence for sex transformation of Macrobrachium rosenbergii and an application thereof. Background technique [0002] Macrobrachium rosenbergii (Macrobrachium rosenbergii) belongs to the phylum Arthropoda, Crustacea, Order Decapod, Gibrachidae, Macrobrachium genus, and is a large freshwater prawn. Macrobrachium rosenbergii belongs to tropical and subtropical shrimps. It is distributed in freshwater and brackish waters of the Indian Ocean and Pacific Ocean. It is mainly distributed in Asia, especially in Southeast Asian countries, such as India, Thailand, Myanmar, Indonesia, and Malaysia. Macrobrachium rosenbergii is one of the most important freshwater prawn species in the world. [0003] The androgenic gland (AG) is an endocrine organ unique to male crustaceans, which was first discovered in the blue crab (Callinectessapidus) [1] . F...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/113A01K67/033
CPCA01K67/0338A01K2207/05A01K2227/70C12N15/1138C12N2310/14
Inventor 王卫民陈健安
Owner HUAZHONG AGRI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com