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Reagent kit for detecting 1586T>G mutation of large vestibular aqueduct related gene SLC26A4

A SLC26A4, kit technology, applied in recombinant DNA technology, microbial assay/inspection, DNA/RNA fragments, etc., can solve problems such as changes in membrane labyrinth structure

Inactive Publication Date: 2008-08-20
GENERAL HOSPITAL OF PLA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

And due to toxic mechanisms of altered osmotic pressure and altered composition lead to altered membrane labyrinth structure

Method used

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  • Reagent kit for detecting 1586T>G mutation of large vestibular aqueduct related gene SLC26A4
  • Reagent kit for detecting 1586T>G mutation of large vestibular aqueduct related gene SLC26A4
  • Reagent kit for detecting 1586T>G mutation of large vestibular aqueduct related gene SLC26A4

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0067] [Example 1] Detection method for 109G>T heterozygous mutation of SLC26A4 gene

[0068] 1. Preparation of blood sample DNA of the subject to be tested

[0069] 1. Research objects: 89 patients with enlarged vestibular aqueduct collected from the deaf outpatient clinic, and 80 normal controls. All participants were investigated in detail about their medical history and family history, and a physical examination was performed on them. The otological examination included otoscopy and audiological evaluation. After signing the informed consent form, 5-10ml blood samples were collected from each person.

[0070] 2. Genomic DNA extraction: using phenol-chloroform extraction method.

[0071] first day

[0072] 1) Anticoagulant blood was diluted 1-fold with PBS.

[0073] 2) Add 2 times the volume of lymphatic separation solution (18°C-28°C) into the centrifuge tube, spread a layer of 1 times the volume of diluted blood on top, centrifuge at 1000×g at room temperature for 20 ...

Embodiment 2

[0150] [Example 2] Research on the evolution of mutation sites

[0151] Mutation analysis: sequence comparison analysis was performed using SeqmanTM software in the DNAStar5.0 (Lasergene Inc.) software package. The sequence obtained by sequencing was compared with the standard sequence retrieved by NCBI to find out the mutant sequence and the mutation site (109G>T, E37X).

[0152] Evolutionary study: The 109G>T mutation is located at the amino terminal of Pendrin, which terminates the amino acid code at position 37, and the subsequent 734 amino acids are lost. This mutation must affect the structure and function of Pendrin.

[0153] Detection of 1586T>G heterozygous mutation in SLC26A4 gene

[0154] A patient with an enlarged vestibular aqueduct was used as the research object. Through the screening of the exons in the coding region of the SLC26A4 gene in 89 family members of the disease and 80 normal controls, it was found that a patient with an enlarged vestibular aqueduct...

Embodiment 3

[0155] [Example 3] Detection method for 1586T>G heterozygous mutation of SLC26A4 gene

[0156] See Example 1 for basic methods and steps. The PCR amplification primer sequence for exon 14 of SLC26A4 gene is:

[0157] Upstream primers:

[0158] PDS14-F: 5'-TGCTCATTATTTCTCTCA-3'(nt37174-nt37191)

[0159] Downstream primers:

[0160] PDS14-R: 5'-TTTTCTCCCTTTGGCTAC-3'(nt37555-nt37572)

[0161] Note: SLC26A4 gene sequence retrieval number: Gene ID: 5172

[0162] The PCR reaction process is shown in FIG. 8 ; the agarose gel electrophoresis pattern of electrophoresis and quantification of the PCR products is shown in FIG. 9 ; and the sequencing map is shown in FIG. 10 .

[0163] Enzyme digestion reaction detection of mutation sites

[0164] The composition of the enzyme digestion reaction system is shown in Table 4, and the reaction condition is 37°C water bath for 3 hours. For detection by agarose electrophoresis, refer to the electrophoresis quantification in Example 1 for t...

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Abstract

The invention relates to a detection method, whether a sample from an individual to be tested has the SLC26A4 gene mutation or not is detected, so as to diagnose the occurrence and the type of the large vestibular aqueduct of the individual to be tested, wherein, the SLC26A4 gene mutation is the heterozygous mutation of 1586T which is larger than G of a gene exon 14 which is positioned at SLC26A4. The invention also relates to a detection kit for detecting whether the sample from the individual to be tested has the SLC26A4 gene mutation and an application of theSLC26A4 gene mutation in the diagnosis and / or the treatment of the diseases which are related to the large vestibular aqueduct. The gene mutation and the detection method can be beneficial to the clinical development of the SLC26A4 gene mutation screening work of the deaf patients, thus providing the services for the diagnosis and the treatment of the deaf patients.

Description

[0001] This application is a divisional application of Chinese patent application 200510132214.5. technical field [0002] The invention relates to a kit for detecting SLC26A4 mutation gene. Background technique [0003] The SLC26A4 gene is located at 7q31, which was originally located by Everett et al., and found that the mutation of this gene can lead to an autosomal recessive genetic disease: Pendred syndrome, clinical manifestations of goitre, and combined vestibular aqueduct enlargement or Mondini malformation ( Enlarged vestibular aqueduct combined with cochlear hypoplasia) sensorineural deafness. Later, Usami et al. screened the SLC26A4 gene in 6 families with simple vestibular aqueduct enlargement, showing that the mutation of this gene can also lead to simple vestibular aqueduct enlargement, and its genetic mode is also recessive inheritance. It can be seen that the SLC26A4 gene mutation Can cause vestibular aqueduct enlargement - pure vestibular aqueduct enlargeme...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68C12N15/11
Inventor 王秋菊赵亚丽
Owner GENERAL HOSPITAL OF PLA
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