{"title":"一个原发痛风家系的全基因组测序结果和初步分析","authors":"Xiaoyu Cheng, R. Sun, Tian Liu, Lidan Ma, Ying Xin, Ying Chen, Changgui Li, Zhao-tong Jia","doi":"10.3760/CMA.J.ISSN.1000-6699.2020.02.003","DOIUrl":null,"url":null,"abstract":"Objective \nTo screen gene mutation information of gout pedigree through whole genome sequencing and to carry out preliminary analysis. \n \n \nMethods \nOne typical gout pedigree was selected as the study subjects. The clinical data and the peripheral blood samples were collected and constructed charts of the pedigree. DNAs were extracted from peripheral blood and analyzed by the whole genome sequencing, and by the software analysis and comparison, screening out the pathogenic genes and related mutations. Then the verifications were conducted in the family members and the controls. Bioinformatics software was applied to predict the effect of mutation on gene expression. \n \n \nResults \nBased on the sequencing results, advanced informational analysis was performed to screen out the mutations 1040-8 A> G near the 5 ′end near the exon 8 of the PLAA gene. The results showed that all the gout patients in the family had 1040 -8 A> G sites, and none of the mutants were found in the non-gout group and 200 controls; bioinformatics analysis suggested that the mutation could affect PLAA gene expression, but not affecting PLAA mRNA structure. \n \n \nConclusion \nPLAA gene 1040-8 A> G mutation is separated from patients in the gout pedigree, and the newly discovered PLAA gene may act as a gout pathogenic gene. \n \n \nKey words: \nGout; Pedigree; Whole genome sequencing; Gene","PeriodicalId":10120,"journal":{"name":"中华内分泌代谢杂志","volume":"36 1","pages":"106-110"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A whole genome sequencing result and preliminary analysis of a primary gout pedigree\",\"authors\":\"Xiaoyu Cheng, R. Sun, Tian Liu, Lidan Ma, Ying Xin, Ying Chen, Changgui Li, Zhao-tong Jia\",\"doi\":\"10.3760/CMA.J.ISSN.1000-6699.2020.02.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo screen gene mutation information of gout pedigree through whole genome sequencing and to carry out preliminary analysis. \\n \\n \\nMethods \\nOne typical gout pedigree was selected as the study subjects. The clinical data and the peripheral blood samples were collected and constructed charts of the pedigree. DNAs were extracted from peripheral blood and analyzed by the whole genome sequencing, and by the software analysis and comparison, screening out the pathogenic genes and related mutations. Then the verifications were conducted in the family members and the controls. Bioinformatics software was applied to predict the effect of mutation on gene expression. \\n \\n \\nResults \\nBased on the sequencing results, advanced informational analysis was performed to screen out the mutations 1040-8 A> G near the 5 ′end near the exon 8 of the PLAA gene. The results showed that all the gout patients in the family had 1040 -8 A> G sites, and none of the mutants were found in the non-gout group and 200 controls; bioinformatics analysis suggested that the mutation could affect PLAA gene expression, but not affecting PLAA mRNA structure. \\n \\n \\nConclusion \\nPLAA gene 1040-8 A> G mutation is separated from patients in the gout pedigree, and the newly discovered PLAA gene may act as a gout pathogenic gene. \\n \\n \\nKey words: \\nGout; Pedigree; Whole genome sequencing; Gene\",\"PeriodicalId\":10120,\"journal\":{\"name\":\"中华内分泌代谢杂志\",\"volume\":\"36 1\",\"pages\":\"106-110\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中华内分泌代谢杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1000-6699.2020.02.003\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华内分泌代谢杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1000-6699.2020.02.003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
摘要
目的通过全基因组测序筛选痛风家系基因突变信息并进行初步分析。方法选择1个典型的痛风家系作为研究对象。收集临床资料和外周血标本,建立家系图。提取外周血dna进行全基因组测序分析,通过软件分析比较,筛选出致病基因及相关突变。然后在家庭成员和对照组中进行验证。应用生物信息学软件预测突变对基因表达的影响。结果基于测序结果,进行了深入的信息分析,筛选出PLAA基因8外显子5′端附近的1040-8 A> G突变。结果表明,家族中所有痛风患者均有1040 ~ 8个A>个G位点,非痛风组和200个对照组均未发现突变体;生物信息学分析表明该突变可影响PLAA基因表达,但不影响PLAA mRNA结构。结论在痛风家系患者中分离到PLAA基因1040- 8a >g突变,新发现的PLAA基因可能是痛风致病基因。关键词:痛风;血统;全基因组测序;基因
A whole genome sequencing result and preliminary analysis of a primary gout pedigree
Objective
To screen gene mutation information of gout pedigree through whole genome sequencing and to carry out preliminary analysis.
Methods
One typical gout pedigree was selected as the study subjects. The clinical data and the peripheral blood samples were collected and constructed charts of the pedigree. DNAs were extracted from peripheral blood and analyzed by the whole genome sequencing, and by the software analysis and comparison, screening out the pathogenic genes and related mutations. Then the verifications were conducted in the family members and the controls. Bioinformatics software was applied to predict the effect of mutation on gene expression.
Results
Based on the sequencing results, advanced informational analysis was performed to screen out the mutations 1040-8 A> G near the 5 ′end near the exon 8 of the PLAA gene. The results showed that all the gout patients in the family had 1040 -8 A> G sites, and none of the mutants were found in the non-gout group and 200 controls; bioinformatics analysis suggested that the mutation could affect PLAA gene expression, but not affecting PLAA mRNA structure.
Conclusion
PLAA gene 1040-8 A> G mutation is separated from patients in the gout pedigree, and the newly discovered PLAA gene may act as a gout pathogenic gene.
Key words:
Gout; Pedigree; Whole genome sequencing; Gene
中华内分泌代谢杂志Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
0.60
自引率
0.00%
发文量
7243
期刊介绍:
The Chinese Journal of Endocrinology and Metabolism was founded in July 1985. It is a senior academic journal in the field of endocrinology and metabolism sponsored by the Chinese Medical Association. The journal aims to be the "Chinese broadcaster of new knowledge on endocrinology and metabolism worldwide". It reports leading scientific research results and clinical diagnosis and treatment experience in endocrinology and metabolism and related fields, as well as basic theoretical research that has a guiding role in endocrinology and metabolism clinics and is closely integrated with clinics. The journal is a core journal of Chinese science and technology (a statistical source journal of Chinese science and technology papers), and is included in Chinese and foreign statistical source journal databases such as the Chinese Science and Technology Papers and Citation Database, Chemical Abstracts, and Scopus.