Method for making insertional mutations

A technology of insertion mutation and synapse, which can be applied to other methods of inserting foreign genetic materials, mutant preparation, botanical equipment and methods, etc., and can solve the problems of complicated and unsatisfactory insertion mutation library analysis.

Inactive Publication Date: 2008-09-24
WISCONSIN ALUMNI RES FOUND
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This unwanted redundant transposition is undesirable and complicates the analysis of insertional mutant libraries

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
  • Method for making insertional mutations
  • Method for making insertional mutations
  • Method for making insertional mutations

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0035] In a 1 μl, 0.05 μg purified hyperactive transposase (EK54 / MA56 / LP372) reaction, the amino acid sequence disclosed in the international application PCT / US97 / 15941 cited herein was combined with 0.1 μg transposable polynucleotide, the transposable polynucleotide The locus polynucleotide contains an expression cassette encoding a protein that confers kanamycin resistance to target cells. This expression cassette is flanked by spliced ​​ends (as described in the same international application cited) and is shown in Figure 3. Separated The polynucleotide was provided in a reaction in , either as a supercoiled plasmid, a linearized plasmid, or as a fragment of the polynucleotide including the reverse sequence required for Tn5 transposase-mediated transposition at its terminus.

[0036] With or without magnesium ions (Mg ++ ) in reaction buffer for 1 hour. In the absence of magnesium ions, synaptic complexes formed in vitro but no transposition occurred.

[0037] After incuba...

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

A method for making insertional mutations at random or quasi-random locations in the chromosomal or extra-chromosomal nucleic acid of a target cell includes the step of combining, in the target cell, cellular nucleic acid with a synaptic complex that comprises (a) a Tn5 transposase protein and (b) a polynucleotide that comprises a pair of nucleotide sequences adapted for operably interacting with Tn5 transposase and a transposable nucleotide sequence therebetween, under conditions that mediate transpositions into the cellular DNA. In the method, the synaptic complex is formed in vitro under conditions that disfavor or prevent the synaptic complexes from undergoing productive transposition.

Description

[0001] There are no applicable cross-referenced related applications. [0002] No applicable jointly proposed research or development literature. Background of the invention [0003] Efficient insertion of exogenous nucleic acids into chromosomal and extrachromosomal nucleic acids of cells is a desired technique in the field of molecular biology to identify chromosomal regions involved in expressing peptides and proteins or regulating their expression. It can also be used advantageously in the development of novel therapeutics and pharmaceuticals as well. [0004] A commonly used method relies on in vivo Tn5 mutagenesis to insert a polynucleotide of interest into cellular DNA and construct a library of cells containing the inserted polynucleotide at random or quasi-random positions. The in vivo Tn5 mutagenesis approach requires the target cell to encode a transposase, whether native or produced from an introduced expression construct. In addition, it may be necessary to cons...

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): C12N15/10C12N15/55C12N15/90C12N9/22G01N33/50C12N9/00C12N15/00C12N15/01C12N15/09C12Q1/02G01N33/15G01N33/566
CPCC12N15/102C12N15/90C12N9/22
Inventor W·S·列兹尼科夫I·Y·戈雷申
Owner WISCONSIN ALUMNI RES FOUND
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap