GJB2单杂合突变非综合征型耳聋患者GJB2序列长度检测  被引量:2

Detection of GJB2 Gene Sequence Length in Patients with Nonsyndromic Deafness and Monoallelic GJB2 Gene Mutations

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作  者:王辉兵[1,2] 于飞[1] 戴朴[1,3] 单希征[2] 袁永一[1] 张昕[1] 康东洋[1] 韩东一[1] 

机构地区:[1]解放军总医院耳鼻咽喉头颈外科,解放军耳鼻咽喉科研究所,北京100853 [2]武警总医院耳鼻咽喉头颈外科,北京100039 [3]解放军总医院海南分院耳鼻咽喉头颈外科,海南572000

出  处:《中华耳科学杂志》2014年第1期54-56,共3页Chinese Journal of Otology

基  金:国家十二五支撑项目(2012BAI09B00,2012BAI12B01);国家自然科学基金重点项目(81230020);国家自然科学基金面上项目(81371096,81371098);国家自然科学基金青年项目(30801285);卫生部行业专项基金(201202005);北京市自然科学基金面上项目(7132177,7122172);北京市科技新星计划(2009B34,2010B081);国家高技术研究发展计划(“863”,2012AA020101)

摘  要:目的检测GJB2单杂合突变非综合征型耳聋患者GJB2全序列中是否有大片段的碱基插入或缺失,研究GJB2全序列长链PCR方法和电泳方法。方法应用长链PCR方法对201例GJB2单杂合突变非综合征型耳聋患者进行GJB2全序列长度检测,对照组为111例听力正常的成年人。应用两步法PCR,调整加入DNA模板量、PCR延伸时间、循环次数等,0.8%琼脂糖凝胶电泳检测PCR产物的长度和量,调整加样槽的宽度、加样量、电泳电压、电流、电泳时间得到清晰条带,若PCR产物存在大片段碱基插入或缺失,用限制性内切酶BamHI进行内切酶反应,初步判断插入或缺失的大致位置。结果 201例GJB2单杂合突变患者中,GJB2序列长度未见大片段碱基插入或缺失。对照组GJB2序列长度未见异常。结论 GJB2单杂合突变非综合征型耳聋患者中GJB2序列长度检测未见明显异常。Objective To detect whether or not does inse^ion or deletion of large fragment nucleotides exist in GJB2 gene for the NSHI (nonsyndromic hearing impairment) patients with monoallelic GJB2 Gene Mutations, and to study long chain PCR method and electrophoresis for the full sequence length of GJB2 gene. Methods We detected the sequence length of GJB2 gene for 201 patients with monoallelic GJB2 gene mutations and 111 cases of control group with normal hearing by long chain PCR method. The product amount of PCR was adjusted by the amount of the DNA template, the extension time and the cycles of PCR. The sequence length of PCR product of the GJB2 gene was detected by 0.8% agarose gel electrophoresis. To ob- tain a clear electrophoresis strip, we changed the width of the well, the volume of sample of PCR product, the electrophoresis voltage and current, electrophoresis time, etc. If the sequence length of PCR products had obviously increase or decrease, there could exist insertion or deletion of large fragment nucleotide in the GJB2 gene sequence. We determined the approximate loca- tion of the insertion or deletion by restriction enzyme reaction of BamHI enzyme. Results We didn' t detect obvious increase or decrease of the sequence length of GJB2 gene in 201 patients with monoallelic GJB2 gene mutations and in the control group. Conclusion Insertion or deletion of large fragment nucleotide in GJB2 gene sequence was not detected in NSHI pa- tients with monoallelic GJB2 gene mutations.

关 键 词:非综合征型耳聋 GJB2基因 单杂合突变 序列长度 

分 类 号:R764.43[医药卫生—耳鼻咽喉科] R764.04[医药卫生—临床医学]

 

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