研究报告

基于全基因组数据的AI-SNPs筛选及大陆次级区域内群体遗传结构差异研究

展开
  • 四川大学华西基础医学与法医学院,成都 610041
王浩宇,在读硕士研究生,专业方向:法医物证学。E-mail: wanghy0707@gmail.com;|胡渝涵,在读硕士研究生,专业方向:法医物证学。E-mail: huyuhan28@163.com; 王浩宇和胡渝涵并列第一作者。

收稿日期: 2021-05-26

  修回日期: 2021-07-23

  网络出版日期: 2021-08-04

基金资助

国家自然科学基金项目资助编号(81571861);国家自然科学基金项目资助编号(81630054)

AI-SNPs screening based on the whole genome data and research on genetic structure differences of subcontinent populations

Expand
  • West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu 610041, China

Received date: 2021-05-26

  Revised date: 2021-07-23

  Online published: 2021-08-04

Supported by

Supported by the National Natural Science Foundation of China Nos(81571861);Supported by the National Natural Science Foundation of China Nos(81630054)

摘要

在涉及多群体样本的医学研究中,群体遗传结构差异是不容忽视的影响因素之一。利用族源信息单核苷酸多态性遗传标记(ancestry-informative single nucleotide polymorphism, AI-SNP),通过分析群体遗传成分、推断个体遗传背景并对群体样本进行预筛选,可以有效降低群体遗传结构差异对医学研究影响。鉴于已发表的研究多为解析大陆间、大陆次级区域间的群体遗传结构差异,本研究拟基于千人基因组计划(GRCh37.p13)中东亚五群体:日本东京群体(Japanese in Tokyo, JPT)、北京汉族(Han Chinese in Beijing, CHB)、南方汉族(Southern Han Chinese, CHS)、西双版纳傣族(Chinese Dai in Xishuangbanna, CDX)、越南京族(Kinh in Ho Chi Minh City, KHV)的数据,以FST值为标准筛选AI-SNP并分析大陆次级区域内群体遗传结构差异。结果表明,研究涉及的东亚群体可分为三簇:JPT、CHB和CHS、CDX和KHV。利用AI-SNP可成功解析个体的遗传背景,而群体代表性遗传成分占比超过80%的个体具有良好的群体代表性。本研究表明,基于FST值筛选一组AI-SNP用于核验样本遗传背景、筛选群体代表性样本的方法在降低大陆次级区域内群体遗传结构差异对群体相关医学研究的影响中具有实际应用价值。

本文引用格式

王浩宇, 胡渝涵, 曹悦岩, 朱强, 黄雨果, 李茜, 张霁 . 基于全基因组数据的AI-SNPs筛选及大陆次级区域内群体遗传结构差异研究[J]. 遗传, 2021 , 43(10) : 938 -948 . DOI: 10.16288/j.yczz.21-185

Abstract

The genetic structure differences in population is one of the key elements in medical research involving multi-population samples. A set of ancestry-informative single nucleotide polymorphisms (AI-SNPs) can be utilized to analyze genetic component of a population, infer ancestral origin of individuals and pre-filter samples to reduce the impact of population genetic structure differences on medical research. However, most of the published studies were focused on revealing the differences between populations of continents or regions of a continent. In this paper, AI-SNPs were screened by calculating FST value in each pair of five East Asian populations: Japanese in Tokyo (JPT), Han Chinese in Beijing (CHB), Southern Han Chinese (CHS), Chinese Dai in Xishuangbanna (CDX) and Kinh in Ho Chi Minh City (KHV) in the 1000 Genomes Project phase 3 (GRCh37.p13) to analyze differences in subcontinent populations. The results demonstrate that the five East Asian populations in our study were assigned to three clusters: JPT, CHB and CHS, CDX and KHV. A set of AI-SNPs can be used for analysis of individual genetic composition and selection of representative individuals. Individuals with over 80% population representative genetic components have good representativeness of a population. This paper demonstrated the practical value of the method, which was performed to verify the ancestral composition and select representative samples with a panel of screened AI-SNPs by FST value, thereby reducing the influence of genetic structure differences in subcontinent populations on population-related medical research.

参考文献

[1] Hellwege JN, Keaton JM, Giri A, Gao XY, Velez Edwards DR, Edwards TL. Population stratification in genetic association studies. Curr Protoc Hum Genet, 2017, 95: 1.22.1-1.22.23.
[2] Schlebusch CM, Skoglund P, Sj?din P, Gattepaille LM, Hernandez D, Jay F, Li S, De Jongh M, Singleton A, Blum MG, Soodyall H, Jakobsson M . Genomic variation in seven Khoe-San groups reveals adaptation and complex African History. Science, 2012,338(6105):374-379.
[3] Price AL, Zaitlen NA, Reich D, Patterson N . New approaches to population stratification in genome-wide association studies. Nat Rev Genet, 2010,11(7):459-463.
[4] Gong X, Zhang C, Yiliyasi A, Shi Y, Yang XW, Nuersimanguli A, Guan YQ, Xu SH. A comparative analysis of genetic diversity of candidate genes associated with type 2 diabetes in worldwide populations. Hereditas (Beijing), 2016,38(6):544-565.
[4] 弓弦, 张超, 伊利亚斯·艾萨, 时瑛, 杨雪唯, 努尔斯曼古丽·奥斯曼, 关亚群, 徐书华. 2型糖尿病易感候选基因在世界不同人群中的多样性比较分析. 遗传, 2016,38(6):544-565.
[5] Dai R, Zhang C, Cheng YJ, Chen WL, Li Q, Wang YM. Pharmacogenomics genetic differences between Wa and Blang ethnic groups in Yunnan. J Kunming Med Univ, 2020,41(5):33-40.
[5] 代润, 张婵, 程瑜静, 陈婉璐, 李琦, 王玉明. 云南佤族和布朗族人群药物基因组学基因遗传差异. 昆明医科大学学报, 2020,41(5):33-40.
[6] Phillips C, Prieto L, Fondevila M, Salas A, Gómez-Tato A, Alvarez-Dios J, Alonso A, Blanco-Verea A, Brión M, Montesino M, Carracedo A, Lareu MV . Ancestry analysis in the 11-M Madrid bomb attack investigation. PLoS One, 2009,4(8):e6583.
[7] Tian C, Plenge RM, Ransom M, Lee A, Villoslada P, Selmi C, Klareskog L, Pulver AE, Qi LH, Gregersen PK, Seldin MF . Analysis and application of European genetic substructure using 300 K SNP information. PLoS Genet, 2008,4(1):e4.
[8] Enoch MA, Shen PH, Xu K, Hodgkinson C, Goldman D . Using ancestry-informative markers to define populations and detect population stratification. J Psychopharmacol, 2006,20(4):19-26.
[9] Pritchard JK, Stephens M, Rosenberg NA, Donnelly P . Association mapping in structured populations. Am J Hum Genet, 2000,67(1):170-181.
[10] Clarke L, Fairley S, Zheng-Bradley X, Streeter I, Perry E, Lowy E, Tassé AM, Flicek P . The international genome sample resource (IGSR): a worldwide collection of genome variation incorporating the 1000 genomes project data. Nucleic Acids Res, 2017,45(D1):D854-D859.
[11] 1000 Genomes Project Consortium, Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR . A global reference for human genetic variation. Nature, 2015,526(7571):68-74.
[12] Qin PF, Li ZQ, Jin WF, Lu DS, Lou HY, Shen JW, Jin L, Shi YY, Xu SH . A panel of ancestry informative markers to estimate and correct potential effects of population stratification in Han Chinese. Eur J Hum Genet, 2014,22(2):248-253
[13] Severe Covid-19 GWAS Group, Ellinghaus D, Degenhardt F, Bujanda L, Buti M, Albillos A, Invernizzi P, Fernández J, Prati D, Baselli G, Asselta R, Grimsrud MM, Milani C, Aziz F, K?ssens J, May S, Wendorff M, Wienbrandt L, Uellendahl-Werth F, Zheng TH, Yi XL, de Pablo R, Chercoles AG, Palom A, Garcia-Fernandez AE, Rodriguez- Frias F, Zanella A, Bandera A, Protti A, Aghemo A, Lleo A, Biondi A, Caballero-Garralda A, Gori A, Tanck A, Carreras Nolla A, Latiano A, Fracanzani AL, Peschuck A, Julià A, Pesenti A, Voza A, Jiménez D, Mateos B, Nafria Jimenez B, Quereda C, Paccapelo C, Gassner C, Angelini C, Cea C, Solier A, Pesta?a D, Mu?iz-Diaz E, Sandoval E, Paraboschi EM, Navas E, García Sánchez F, Ceriotti F, Martinelli-Boneschi F, Peyvandi F, Blasi F, Téllez L, Blanco-Grau A, Hemmrich-Stanisak G, Grasselli G, Costantino G, Cardamone G, Foti G, Aneli S, Kurihara H, ElAbd H, My I, Galván-Femenia I, Martín J, Erdmann J, Ferrusquía-Acosta J, Garcia-Etxebarria K, Izquierdo- Sanchez L, Bettini LR, Sumoy L, Terranova L, Moreira L, Santoro L, Scudeller L, Mesonero F, Roade L, Rühlemann MC, Schaefer M, Carrabba M, Riveiro-Barciela M, Figuera Basso ME, Valsecchi MG, Hernandez-Tejero M, Acosta-Herrera M, D'Angiò M, Baldini M, Cazzaniga M, Schulzky M, Cecconi M, Wittig M, Ciccarelli M, Rodríguez-Gandía M, Bocciolone M, Miozzo M, Montano N, Braun N, Sacchi N, Martínez N, ?zer O, Palmieri O, Faverio P, Preatoni P, Bonfanti P, Omodei P, Tentorio P, Castro P, Rodrigues PM, Blandino Ortiz A, de Cid R, Ferrer R, Gualtierotti R, Nieto R, Goerg S, Badalamenti S, Marsal S, Matullo G, Pelusi S, Juzenas S, Aliberti S, Monzani V, Moreno V, Wesse T, Lenz TL, Pumarola T, Rimoldi V, Bosari S, Albrecht W, Peter W, Romero-Gómez M, D'Amato M, Duga S, Banales JM, Hov JR, Folseraas T, Valenti L, Franke A, Karlsen TH . Genomewide association study of Severe Covid-19 with respiratory failure. N Engl J Med, 2020,383(16):1522-1534.
[14] Foo JN, Tan LC, Irwan ID, Au WL, Low HQ, Prakash KM, Ahmad-Annuar A, Bei JX, Chan AY, Chen CM, Chen YC, Chung SJ, Deng H, Lim SY, Mok V, Pang H, Pei Z, Peng R, Shang HF, Song K, Tan AH, Wu YR, Aung T, Cheng CY, Chew FT, Chew SH, Chong SA, Ebstein RP, Lee J, Saw SM, Seow A, Subramaniam M, Tai ES, Vithana EN, Wong TY, Heng KK, Meah WY, Khor CC, Liu H, Zhang F, Liu J, Tan EK . Genome-wide association study of Parkinson's disease in East Asians. Hum Mol Genet, 2017,26(1):226-232.
[15] Setakis E, Stirnadel H, Balding DJ . Logistic regression protects against population structure in genetic association studies. Genome Res, 2006,16(2):290-296.
[16] Gaspar HA, Breen G . Probabilistic ancestry maps: a method to assess and visualize population substructures in genetics. BMC Bioinformatics, 2019,20(1):116.
[17] Pritchard JK, Stephens M, Donnelly P . Inference of population structure using multilocus genotype data. Genetics, 2000,155(2):945-959.
[18] Alexander DH, Novembre J, Lange K . Fast model-based estimation of ancestry in unrelated individuals. Genome Res, 2009,19(9):1655-1664.
[19] Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D . Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet, 2006,38(8):904-909.
[20] Phillips C, Salas A, Sánchez JJ, Fondevila M, Gómez-Tato A, Alvarez-Dios J, Calaza M, de Cal MC, Ballard D, Lareu MV, Carracedo A; SNPforID Consortium. Inferring ancestral origin using a single multiplex assay of ancestry-informative marker SNPs. Forensic Sci Int Genet, 2007,1(3-4):273-80.
[21] Li CX, Pakstis AJ, Jiang L, Wei YL, Sun QF, Wu H, Bulbul O, Wang P, Kang LL, Kidd JR, Kidd KK . A panel of 74 AISNPs: improved ancestry inference within Eastern Asia. Forensic Sci Int Genet, 2016,23:101-110.
[22] Liu j, Liu CC, Ma M, Wang L, Zhao WT, Ma Q, Ji AQ, Liu J, Li CX. The ancestry inference of Chinese populations using 74-plex SNPs system. Hereditas (Beijing), 2020,42(3):296-308.
[22] 刘杨, 孙昌春, 马咪, 王玲, 赵雯婷, 马泉, 季安全, 刘京, 李彩霞. 74-plex SNPs复合检测体系在中国人群中的族群推断研究. 遗传, 2020,42(3):296-308.
[23] Qu SQ, Zhu J, Wang YJ, Yin L, Lv ML, Wang L, Jian H, Tan Y, Zhang RR, Liu YQ, Li F, Huang SC, Liang WB, Zhang L . Establishing a second-tier panel of 18 ancestry informative markers to improve ancestry distinctions among Asian populations. Forensic Sci Int Genet, 2019,41:159-167.
[24] Bulbul O, Speed WC, Gurkan C, Soundararajan U, Rajeevan H, Pakstis AJ, Kidd KK . Improving ancestry distinctions among Southwest Asian populations. Forensic Sci Int Genet, 2018,35:14-20.
[25] Shi CM, Liu Q, Zhao SL, Chen H . Ancestry informative SNP panels for discriminating the major East Asian populations: Han Chinese, Japanese and Korean. Ann Hum Genet, 2019,83(5):348-354
[26] Danecek P, Auton A, Abecasis G, Albers CA, Banks E, DePristo MA, Handsaker RE, Lunter G, Marth GT, Sherry ST, McVean G, Durbin R; 1000 Genomes Project Analysis Group. The variant call format and VCFtools. Bioinformatics, 2011,27(15):2156-2158.
[27] Weir BS, Cockerham CC . Estimating F-statistics for the analysis of population structure. Evolution, 1984,38(6):1358-1370.
[28] Falush D, Stephens M, Pritchard JK . Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. Genetics. 2003,164(4):1567-87.
[29] Earl DA, vonHoldt BM . Structure Harvester: a website and program for visualizing structure output and implementing the Evanno method. Conserv Genet Resour, 2012,4(2):359-361.
[30] Jakobsson M, Rosenberg NA . Clumpp: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure. Bioinformatics, 2007,23(14):1801-1806.
[31] Rosenberg NA . Distructd: a program for the graphical display of population structure. Mol Ecol Notes, 2004,4(1):137-138.
[32] Zhou CX, Li M, Huai C, He L, Qin SY. Study on hereditary susceptibility genetic markers to anti-tuberculosis drug induced liver injury in Chinese population. Hereditas (Beijing), 2020,42(4):374-379.
[32] 周晨希, 李沫, 怀聪, 贺林, 秦胜营. 中国人群中抗结核药物引发肝损伤的易感基因标记研究. 遗传, 2020,42(4):374-379.
[33] Sun YD, Tian ZZ, Zhou W, Li M, Huai C, He L, Qin SY. Genome-wide association study on liver function tests in Chinese. Hereditas(Beijing), 2021,43(3):249-260.
[33] 孙一丹, 田子钊, 周伟, 李沫, 怀聪, 贺林, 秦胜营. 中国人群肝功能检测指标全基因组关联分析研究. 遗传, 2021,43(3):249-260.
[34] Wright S . The genetical structure of populations. Nature, 1951,15(4):323-354.
[35] Holsinger KE, Weir BS . Genetics in geographically structured populations: defining, estimating and interpreting F(ST). Nat Rev Genet, 2009,10(9):639-650.
[36] Santos C, Phillips C, Gomez-Tato A, Alvarez-Dios J, Carracedo á, Lareu MV . Inference of ancestry in forensic analysis II: analysis of genetic data. Methods Mol Biol. 2016,1420:255-285.
文章导航

/