Application of mutated gene PRPF4 in preparation of hereditary retinal disease diagnosis reagent

A technology for retinal diseases and diagnostic reagents, which is applied in the field of preparation of diagnostic reagents for hereditary retinal diseases, can solve the problems of screening out disease-causing genes, failing to locate disease-causing sites, and difficult to analyze small families and sporadic cases, etc., to achieve The effect of wide screening area and high screening efficiency

Active Publication Date: 2014-08-27
赵晨
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  • Abstract
  • Description
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AI Technical Summary

Problems solved by technology

The positional cloning strategy based on linkage analysis is a classic method to identify the causative genes of single-gene genetic diseases, but it also faces some difficulties: ① usually requires multi-generation families, and it is difficult to analyze small families and sporadic cases
②Sometimes multi-generational families cannot locate the pathogenic locus
③ It is difficult to screen out the correct disease-causing gene in the linkage region

Method used

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  • Application of mutated gene PRPF4 in preparation of hereditary retinal disease diagnosis reagent
  • Application of mutated gene PRPF4 in preparation of hereditary retinal disease diagnosis reagent
  • Application of mutated gene PRPF4 in preparation of hereditary retinal disease diagnosis reagent

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] experimental method:

[0049] 1. Establishment of HRDs genetic resource bank.

[0050] 1.1 Collect the clinical data and blood samples of the following three types of patients:

[0051] 1.1.13 or more generations of autosomal dominant, autosomal recessive, and X-linked recessive families, including RP, Leber congenital amaurosis, congenital static night blindness, and yolk-like macular dystrophy , Stargardt disease.

[0052] 1.1.2 Collect small hereditary families of various HRDs.

[0053] 1.1.3 Collect sporadic cases of various HRDs without family history.

[0054] 1.2 Genomic DNA extraction:

[0055] Using TIANamp Blood DNA Extraction Kit (Tiangen Biotech Co. Ltd, Beijing, China), the patient's genomic DNA was extracted from the collected patient's peripheral blood according to the protocol provided by the manufacturer.

[0056] 2. Mining new pathogenic genes / new mutations of known pathogenic genes in HRDs (see figure 2 ).

[0057] 2.1 Design and customize HRDs...

Embodiment 2

[0092] Functional research was carried out on the pathogenic gene detected in Example 1. Here, the new mutation p.P315L of the above-mentioned PRPF4 gene was taken as an example.

[0093] experimental method:

[0094] 1. Conservative analysis:

[0095] Using NCBI HomoloGene database ( http: / / www.ncbi.nlm.nih.gov / homologene ) Conservative prediction of the screened mutations in multiple species.

[0096] 2. Predict the pathogenicity of mutations based on SIFT and PolyPhen values:

[0097] Using two mainstream online prediction software: PolyPhen-2 (Polymorphism Phenotyping, version2; http: / / genetics.bwh.harvard.edu / pph2 / ) and SIFT Human Protein DB ( http: / / sift.bii.a-star.edu.sg / ), to predict the impact of missense mutations and nonsense mutations on protein levels, thereby predicting the pathogenicity of mutations.

[0098] 3. Research on protein crystal structure changes:

[0099] Since the PRPF4 gene is involved in the formation of the U4 / U6 complex, and the mutat...

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Abstract

The invention discloses an application of mutated gene PRPF4 in the preparation of a hereditary retinal disease diagnosis reagent. A method for screening HRDs virulence gene comprises the following steps: 1, establishing an HRDs genetic resource library; 2, designing and synthesizing the gene chip hybridization probe of the HRDs virulence gene, and integrating the gene chip hybridization probe to a gene chip; 3, capturing a target area by using the made gene chip, and carrying out deep sequencing; 4, carrying out bioinformatics analysis on sequenced data, and screening candidate gene chip virulence gene; and 5, carrying out function predication on new found shear gene mutation sites. In the invention, the high-efficiency HRDs target gene capturing technology is established, the deep sequencing is adopted to confirm the HRDs chip capturing efficiency, and an efficient and trusted bioinformation analysis model is established.

Description

[0001] Case Description [0002] This application is a divisional application of a Chinese invention patent application filed on January 7, 2013 with the application number 2013100052529, titled a method for screening pathogenic mutations in HRDs and related gene chip hybridization probe design methods. technical field [0003] The invention belongs to the field of biomedicine and relates to the application of mutated gene PRPF4 in the preparation of diagnostic reagents for hereditary retinal diseases. Background technique [0004] Hereditary retinal diseases (HRDs) are a group of progressive retinal degenerative diseases caused by genetic defects, and are common and serious hereditary blinding diseases in clinical practice. As the number one blindness disease among working-age people worldwide, the incidence of HRDs is about 1 / 3000 in Europe and the United States, and as high as 1 / 1000 in my country. my country is a country with a large number of HRDs genetic resources, bu...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68
CPCC12Q1/6811C12Q1/6869C12Q1/6883C12Q2600/156C12Q2565/519C12Q2535/122
Inventor 赵晨陈雪赵堪兴陈雪娟潘鑫源蒋超
Owner 赵晨
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