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Pathogenic mutation of genetic Usher syndrome and detection reagent thereof

A syndromic and genetic technology, applied in the field of biomedicine, can solve problems such as no reports and few studies.

Active Publication Date: 2016-11-23
赵晨
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The Centrosomal protein of 78 kDa (CEP78) gene is located on chromosome 9. This gene contains 16 exons. The Cep78 protein encoded by it is a centrosomal protein containing 722 amino acids. At present, there are few studies on the function of Cep78 protein. There is no report on the relationship between CEP78 gene mutation and diseases, especially Usher syndrome

Method used

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  • Pathogenic mutation of genetic Usher syndrome and detection reagent thereof
  • Pathogenic mutation of genetic Usher syndrome and detection reagent thereof
  • Pathogenic mutation of genetic Usher syndrome and detection reagent thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0040] Detection of CEP78 gene mutation in a consanguineous Usher syndrome family.

[0041] experimental method:

[0042] 1. Collection of clinical resources of the family and establishment of a genetic resource bank:

[0043] The clinical data and blood samples of the patients in this family were collected, see the family chart figure 1. Clinical data mainly include personal medical history, family history, best corrected visual acuities (BCVAs), slit lamp examination, fundus photography, color vision examination, visual field examination (Humphrey perimetry), full field electroretinography (ERG) ), fundus fluorescein angiography (FFA) and optical coherence tomography (optical coherence tomography; OCT), etc. The blood genomic DNA of each family member was extracted with a blood genomic DNA extraction kit (Qiagen, Hilden, Germany).

[0044] 2. Discover the disease-causing mutation of the patient with the help of high-throughput next-generation sequencing:

[0045] 2.1 De...

Embodiment 2

[0075] Prediction of splicing abnormalities that may be caused by the pathogenic mutation CEP78 c.1629-2A>G detected in Example 1.

[0076] experimental method:

[0077] 1. Prediction of cut site changes:

[0078] The mutation we found is located near the receptor splice site of the intron between exon 14 and exons 13 and 14. For the relationship between the mutation and the normal splice site, see Figure 4 . We used a series of splice site prediction websites to predict possible splice site changes, including:

[0079] (1) Human Splicing Finder, website: http: / / www.umd.be / HSF3 / HSF.html ;

[0080] (2) NetGene2 Server, URL: http: / / www.cbs.dtu.dk / services / NetGene2 / ;

[0081] (3) Splicing Regulation Online Graphical Engine, URL: http: / / sroogle.tau.ac.il / ;

[0082] (4) Berkeley Drosophila Genome Project, website: http: / / www.fruitfly.org / seq_tools / splice.html ;

[0083] (5) SplicePort, URL: http: / / spliceport.cbcb.umd.edu / .

[0084] Experimental results:

...

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Abstract

The invention discloses a pathogenic mutation of a genetic Usher syndrome and a detection reagent thereof. A CEP78 gene for detecting the genetic Usher syndrome is adopted, and the mutation site is the homozygous mutation CEP78c.1629-2A>G of the splice site. The mutation can cause disappearance of a normal splice site and causes changing of the Cep78 protein structure encoded by the CEP78 gene, the CEP78 gene is a new disease-causing gene of the genetic Usher syndrome, and the c.1629-2A>G is a new mutation site, and can be used for preparing the reagent for detecting the genetic Usher syndrome.

Description

technical field [0001] The invention belongs to the field of biomedicine and relates to a pathogenic mutation of hereditary Usher syndrome and a detection reagent thereof. Background technique [0002] Usher syndrome, also known as hereditary deafness retinitis pigmentosa syndrome, retinitis pigmentosa sensorineural deafness syndrome, is an autosomal recessive genetic disease. The main manifestations of Usher syndrome are congenital sensorineural deafness, progressive retinitis pigmentosa, and vision loss. Clinically, Usher syndrome is mainly divided into the following three types: type Ⅰ is congenital severe deep sensorineural deafness, the patient's vestibular response disappears, and retinitis pigmentosa occurs around the age of 10; type Ⅱ is congenital moderate to severe sensorineural deafness Deafness, the vestibular response is normal, and retinitis pigmentosa occurs at the age of 18 to 20; type III is progressive sensorineural deafness, the vestibular response is unc...

Claims

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Application Information

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IPC IPC(8): C12Q1/68C12N15/12
Inventor 赵晨陈雪计江东盛迅伦孙仙桃
Owner 赵晨
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