Method for detecting gene polymorphism SNP (single nucleotide polymorphism) site by utilizing cyclization of RNase H (ribonuclease H)

A gene polymorphism and site technology, applied in biochemical equipment and methods, microbial measurement/inspection, etc., can solve problems such as inactivation and instability, and achieve intuitive data, easy analysis, and fast and accurate results

Inactive Publication Date: 2011-09-14
SHANGHAI JIAO TONG UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the disadvantage of linear RNase H is that it tends to becom

Method used

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  • Method for detecting gene polymorphism SNP (single nucleotide polymorphism) site by utilizing cyclization of RNase H (ribonuclease H)
  • Method for detecting gene polymorphism SNP (single nucleotide polymorphism) site by utilizing cyclization of RNase H (ribonuclease H)
  • Method for detecting gene polymorphism SNP (single nucleotide polymorphism) site by utilizing cyclization of RNase H (ribonuclease H)

Examples

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Embodiment 1

[0044] Identification of the 274th Nucleotide of Human Leukocyte Antigen (HLA)

[0045] In this embodiment, the SNP site to be tested is the 274th nucleotide species of the human leukocyte antigen HLA, the cyclized RNaseH is APE RNase HII, and the probes in the example are C probes and mismatches that match the DNA to be tested. the U probe.

[0046] The first step is to purify the linear APE RNaseHII containing oligoglycine at the N-terminal and the recognition sequence of transpeptidase SortaseA at the C-terminal. The specific steps include:

[0047] 1.1) Design specific primers to mutate the multiple cloning site of the expression vector pTWIN, and mutate the amino acid sequence before the restriction site Not I to oligoglycine;

[0048] 1.2) Design specific primers to introduce the recognition sequence LPXTG of transpeptidase Sortase A into the C-terminus of the protein to be cyclized by PCR amplification;

[0049] 1.3) Select the double restriction sites Not I\Bam H I i...

Embodiment 2

[0060] Thermal Stability Analysis of Circularized Green Fluorescent Protein GFP

[0061] In this example, the activity of transpeptidase Sortase A is utilized to cyclize the green fluorescent protein GFP containing oligoglycine at the N-terminus and the SortaseA recognition sequence LPETG at the C-terminus.

[0062] The first step is to purify the linear GFP containing oligoglycine at the N-terminal and the recognition sequence of transpeptidase Sortase A at the C-terminal. The specific steps include:

[0063] 1.1) Design specific primers to introduce the recognition sequence LPXTG of transpeptidase Sortase A into the C-terminus of the protein to be cyclized by PCR amplification;

[0064] Forward primer: GGGGGGAATTCATGAGTAAAGGAGAAGAACT

[0065] Reverse primer: GGGGGGGATCCTCATCCGGTTTCTGGTAATTTGTATAGTTCATCC

[0066] ATGCC

[0067] 1.2) Select the double restriction sites Not I\Bam H I in the mutant vector pTWIN to construct a protein subclone containing the Sortase A recognit...

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Abstract

The invention relates to a method for detecting a gene polymorphism SNP (single nucleotide polymorphism) site by utilizing cyclization of RNase H (ribonuclease H), which belongs to the technical field of molecular biology. Transpeptidase Sortase A is utilized for cyclization of the linear RNase H, and a probe in the loop-stem structure, a DNA (deoxyribonucleic acid) fragment to be detected, a forward primer and a reverse primer of DNA specificity to be detected, a Vent DNA polymerase and cyclized APERNase H II are further utilized for measuring the specific site SNP of the DNA fragment to be detected, thereby improving the heat stability of the RNase H.

Description

technical field [0001] The invention relates to a method in the field of molecular biology technology, in particular to a method for detecting gene polymorphism SNP sites by using cyclized RNase H. Background technique [0002] Single nucleotide polymorphism (SNP) refers to the polymorphism of the gene sequence caused by the variation of a single nucleotide in the genome. SNPs are widely distributed in the genome, and recent studies have shown that they occur once every 300 base pairs in the human genome. SNP has important application value in the discovery of high-risk groups, the identification of disease-related genes, the design and testing of drugs, and the basic research of biology. Currently, various SNP detection techniques have been developed. However, the existing SNP detection technology is either cumbersome to operate [BioTechniques, 2009, 46: 201-208], or has poor sensitivity [BMC Genomics 2010, 11: 641], or requires expensive detection equipment [Nucleic Acid...

Claims

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Application Information

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IPC IPC(8): C12Q1/68C12Q1/44
Inventor 张琳候敬丽
Owner SHANGHAI JIAO TONG UNIV
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