| 强直性脊柱炎一家系全外显子组测序分析 |
|
摘要点击次数: 2567
全文下载次数: 918
投稿时间：2019-08-21
|
| 作者 | Author | 单位 | Address | E-Mail |
| 任伟凡 |
REN Wei-fan |
杭州市萧山区中医院, 浙江 杭州 311201 |
Xiaoshan District Hospital of Traditional Chinese Medicine in Hangzhou City, Hangzhou 311201, Zhejiang, China |
|
| 胡劲涛 |
HU Jing-tao |
浙江中医药大学, 浙江 杭州 310053 |
|
|
| 高炀 |
GAO Yang |
浙江中医药大学, 浙江 杭州 310053 |
|
|
| 杜伟斌 |
DU Wei-bin |
杭州市萧山区中医院, 浙江 杭州 311201 |
Xiaoshan District Hospital of Traditional Chinese Medicine in Hangzhou City, Hangzhou 311201, Zhejiang, China |
|
| 章何陋 |
ZHANG He-lou |
浙江中医药大学, 浙江 杭州 310053 |
|
|
| 吴奕江 |
WU Yi-jiang |
浙江中医药大学, 浙江 杭州 310053 |
|
|
| 吴风晴 |
WU Feng-qing |
浙江中医药大学, 浙江 杭州 310053 |
|
|
| 柴乐 |
CHAI Le |
浙江中医药大学, 浙江 杭州 310053 |
|
|
| 全仁夫 |
QUAN Ren-fu |
杭州市萧山区中医院, 浙江 杭州 311201 |
Xiaoshan District Hospital of Traditional Chinese Medicine in Hangzhou City, Hangzhou 311201, Zhejiang, China |
quanrenfu@126.com |
|
| 期刊信息：《中国骨伤》2020年，第33卷，第7期，第672-676页 |
| DOI：10.12200/j.issn.1003-0034.2020.07.017 |
| 基金项目:浙江省科技计划项目（编号：2014C03031） |
|
中文摘要:
目的： 对一强直性脊柱炎（ankylosing spondylitis，AS）家系进行全外显子测序，筛选该家系的易感基因，为其发病机制提供理论依据。
方法： 收集1组AS家系成员的临床资料，其中男性患者2例，年龄分别为48岁和18岁，病程分别为23年和4年。提取相关家系成员外周血DNA进行全外显子测序，测序结果与人类数据库比对，过滤掉同义突变及高频突变，整合家系成员单核苷酸非同义突变，寻找致病基因。
结果： 家系成员共得原始数据80 G，数据具有较高质量值，通过对家系患者与正常人测序结果比对分析，同时经过多个生物数据库数据过滤，发现JAK2基因12号外显子上存在的杂合突变c.1709A>G（p.Tyr570Cys）为该家系的可能致病基因突变。另外，该家系MUC3A基因c.1151T>C突变可能是该家系患病成员肠道症状的原因之一。
结论： 运用全基因组外显子测序寻找AS易感基因是可行的，JAK2基因c.1709A>G突变可能是导致该家系AS的致病突变及位点。 |
| 【关键词】脊柱炎,强制性 全外显子组测序 病史采集 |
| |
| Whole-exome sequencing in a pedigree with ankylosing spondylitis |
|
ABSTRACT
Objective: To choose the disease-causing gene in a Chinese pedigree with ankylosing spondylitis (AS) by whole-exome sequencing(WES),and provide theory basis for mechanism of disease.
Methods: Clinical data of AS pedigree were collected,including 2 males,the age were 48 and 18 years old,the course of disease were 23 and 4 years. Whole blood genomic DNA of AS was extracted to perform whole-exome sequencing,the results were compared with human databases,common variations which had been reported were wiped out,then non-synonymous single nucleotide variants(SNVs) from the family members were combined,and candidate genes was selected initially.
Results: Totally 80 G data was obtained from AS family with high quality. By comparing results between patient and normal subject,and filtering with number of biological database,the result showed heterozygous mutation of JAK2 gene 12 exon c.1709 A>G (p.Tyr570Cys) may be the potential disease-causing gene. The variant c.1151T>C of MUC3A gene may be one of the causes of intestinal symptoms in the family members.
Conclusion: It is feasible to find t candidate gene mutations of AS by Exon sequencing. The mutation c.1709 A>G in gene JAK2 identified by whole-exome sequencing might be the pathogenic mutation in this AS pedigree. |
| KEY WORDS Spondylitis,ankylosing Whole exome sequencing Medical history taking |
| |
| 引用本文，请按以下格式著录参考文献： |
| 中文格式: | 任伟凡,胡劲涛,高炀,杜伟斌,章何陋,吴奕江,吴风晴,柴乐,全仁夫.强直性脊柱炎一家系全外显子组测序分析[J].中国骨伤,2020,33(7):672~676 |
| 英文格式: | REN Wei-fan,HU Jing-tao,GAO Yang,DU Wei-bin,ZHANG He-lou,WU Yi-jiang,WU Feng-qing,CHAI Le,QUAN Ren-fu.Whole-exome sequencing in a pedigree with ankylosing spondylitis[J].zhongguo gu shang / China J Orthop Trauma ,2020,33(7):672~676 |
|
| 阅读全文 下载 查看/发表评论 下载PDF阅读器 |
| 关闭 |
|
|
|
