利用全外显子组测序法筛选Leber先天性黑矇一家系候选致病基因的实验研究  

Experimental study on using whole exome sequencing method for screening Leber congenital amaurosis in a family of candidate genes

作　　者：赵军[1] 黄晓生[1] 彭诗茗 祝天辉 贺温玲[1] 曾映虾 范先明[1] 范宝剑[2] Zhao Jun Huang Xiaosheng Peng Shiming Zhu Tianhui He Wenling Zeng Yingxia Fan Xianming Fan Baojian(Shenzhen Eye Hospital Affiliated to Jinan University, Shenzhen Key Laboratory of Ophthalmology, Shenzhen, 518040, China Massachusetts Eye and Ear Infirmary, Harvard Medical School, Ocular Genomics Institute, Boston 02114, United States of America)

机构地区：[1]广东省深圳市眼科医院暨南大学附属深圳眼科医院深圳眼科学重点实验室,518040 [2]哈佛医学院附属麻省眼耳医院眼科基因组学研究所,美国02114

出　　处：《中华眼科医学杂志（电子版）》2017年第1期18-24,共7页Chinese Journal of Ophthalmologic Medicine(Electronic Edition)

基　　金：广东省自然科学基金(S2013010013464);广东省医学科研基金(A2014518);深圳市科技计划项目(JCYJ20140415174819509);深圳市科技计划项目(GJHZ20160229170608241)

摘　　要：目的利用全外显子组测序法筛选Leber先天性黑矇(LCA)一个家系的候选致病基因,为补充或验证LCA致病基因的研究奠定基础。方法采用横断面研究方法。收集一个在深圳市眼科医院就诊的中国汉族LCA家系的临床资料。详细询问并记录全部家系成员的疾病史、家族史及婚育史,并对全部家系成员进行全面的身体检查。其中,眼部检查项目包括视力、眼位、眼压、验光、眼球运动情况、眼前段、眼底照相、光学相干断层扫描及视网膜电图检查等。提取先证者、另外1例患者及其父母的静脉血基因组DNA,采用磁珠提取法对DNA进行提纯。使用高通量测序平台对质量检测通过的DNA文库进行测序。在进行生物信息学分析时,对采集的数据行标准信息分析流程处理,同时对数据进行质控检测。采用GATK基因组分析网络工具库检索单核苷酸多态性位点和缺失标记位点的数量。测序结果经生物信息学分析工具Seattle Seq Annotation138注释后,与人类HAPMAP、db SNP138、Exome Sequencing Project及Exome Aggregation Consortium数据库进行比对。过滤掉已报道的常见变异后,再过滤掉位于非编码区的变异和同义突变,并进一步筛选出该LCA家系的候选致病基因。结果该家系成员共有3代16人。其中,3名LCA患者均为第Ⅱ代成员,第Ⅰ代及第Ⅲ代成员均无发病者,符合常染色体隐性遗传规律。经测序及分析后,得到17个LCA的候选致病基因,分别为ACTN1、C1QTNF3、FAN1、MMP28、MYO9B、NAV1、NUP62、PHLDB3、PRDM12、SLC24A4、ST3GAL3、TCIRG1、TP53、USP54、YIF1B、ZDHHC17及ZNF107。这些基因均与目前已报道的24个LCA相关的致病基因不同。结论对该家系的DNA进行分析后,发现了17个新的LCA候选致病基因,可为进一步明确该家系LCA致病基因的研究奠定了基础。Objective To screen a Leber congenital amaurosis （LCA） pedigree for candidate genes and to provide the research foundation for identification of the pathogenic gene in this pedigree. Methods A cross-sectional study was designed. Clinical data of a Chinese family with LCA collected from Chinese HaM population in Shenzhen Eye Hospital. A detailed inquiry and record all the family members with disease history, family history and obstetrical history, and conduct a comprehensive physical examination of all family members. Among them, the eye examination including visual acuity, eye position, eye movement, anterior segment examination, fundus examination, non-contact intraocular pressure, refraction, fundus photography, optical coherence tomography and electroretinogram. Venous blood genomic DNA was extracted from proband, one patients and their parents. The DNA was purified by magnetic beads extraction method. Sequencing of DNA libraries for quality detection using high-throughput sequencing platforms. Carries on the bioinformatics analysis, collects the data to carry on the standard information analysis processing, concurrently carries on the quality control examination to the data, The number of single nucleotide polymorphism and the number of deletion markers were retrieved using GATK genomic analysis network tool library. The sequencing results were annotated with SeattleSeq Annotation138, and compared with public databases of human HAPMAP, dbSNP138, Exome Sequencing Project and Exome Aggregation Consortium. The candidate genes were identified after common variants, non-coding variants and synonymous mutations were filtered out. Results The LCA pedigree had 3 generations and 16 family members. All patients with LCA were only in the second generation, in accordance with an autosomal recessive inheritance pattern. Seventeen candidate genes were identified, including ACTNI, C1QTNF3, FAN1, MMP28, MYO9B, NAV1, NUP62, PI4LDB3, PRDM12, SLC24A4, ST3CAL3, TCIRG1, TP53, USP54, YIF1B, ZDHHC17 and ZNF107. None of these ca

关 键 词：Leber先天性黑矇 家系 全外显子组测序 候选致病基因 

分 类 号：R774[医药卫生—眼科]