학술논문

Characterization of Large Structural Genetic Mosaicism in Human Autosomes
Document Type
article
Author
Machiela, Mitchell JZhou, WeiyinSampson, Joshua NDean, Michael CJacobs, Kevin BBlack, AmandaBrinton, Louise AChang, I-ShouChen, ChuChen, ConstanceChen, KexinCook, Linda SBou, Marta CrousDe Vivo, ImmaculataDoherty, JenniferFriedenreich, Christine MGaudet, Mia MHaiman, Christopher AHankinson, Susan EHartge, PatriciaHenderson, Brian EHong, Yun-ChulHosgood, H DeanHsiung, Chao AHu, WeiHunter, David JJessop, LeaKim, Hee NamKim, Yeul HongKim, Young TaeKlein, RobertKraft, PeterLan, QingLin, DongxinLiu, JianjunLe Marchand, LoicLiang, XiaolinLissowska, JolantaLu, LingengMagliocco, Anthony MMatsuo, KeitaroOlson, Sara HOrlow, IrenePark, Jae YongPooler, LoreallPrescott, JenniferRastogi, RadhaiRisch, Harvey ASchumacher, FredrickSeow, AdelineSetiawan, Veronica WendyShen, HongbingSheng, XinShin, Min-HoShu, Xiao-OuBerg, David VanDenWang, Jiu-CunWentzensen, NicolasWong, Maria PikWu, ChenWu, TangchunWu, Yi-LongXia, LucyYang, Hannah PYang, Pan-ChyrZheng, WeiZhou, BaosenAbnet, Christian CAlbanes, DemetriusAldrich, Melinda CAmos, ChristopherAmundadottir, Laufey TBerndt, Sonja IBlot, William JBock, Cathryn HBracci, Paige MBurdett, LaurieBuring, Julie EButler, Mary ACarreón, TaniaChatterjee, NilanjanChung, Charles CCook, Michael BCullen, MichaelDavis, Faith GDing, TiDuell, Eric JEpstein, Caroline GFan, Jin-HuFigueroa, Jonine DFraumeni, Joseph FFreedman, Neal DFuchs, Charles SGao, Yu-TangGapstur, Susan MPatiño-Garcia, AnaGarcia-Closas, MontserratGaziano, J MichaelGiles, Graham GGillanders, Elizabeth M
Source
American Journal of Human Genetics. 96(3)
Subject
Biological Sciences
Genetics
Human Genome
Clinical Research
2.1 Biological and endogenous factors
Aetiology
Aged
Chromosome Aberrations
Female
Genome
Human
Genome-Wide Association Study
Genotype
Humans
Male
Middle Aged
Mosaicism
Neoplasms
Medical and Health Sciences
Genetics & Heredity
Biological sciences
Biomedical and clinical sciences
Health sciences
Language
Abstract
Analyses of genome-wide association study (GWAS) data have revealed that detectable genetic mosaicism involving large (>2 Mb) structural autosomal alterations occurs in a fraction of individuals. We present results for a set of 24,849 genotyped individuals (total GWAS set II [TGSII]) in whom 341 large autosomal abnormalities were observed in 168 (0.68%) individuals. Merging data from the new TGSII set with data from two prior reports (the Gene-Environment Association Studies and the total GWAS set I) generated a large dataset of 127,179 individuals; we then conducted a meta-analysis to investigate the patterns of detectable autosomal mosaicism (n = 1,315 events in 925 [0.73%] individuals). Restricting to events >2 Mb in size, we observed an increase in event frequency as event size decreased. The combined results underscore that the rate of detectable mosaicism increases with age (p value = 5.5 × 10(-31)) and is higher in men (p value = 0.002) but lower in participants of African ancestry (p value = 0.003). In a subset of 47 individuals from whom serial samples were collected up to 6 years apart, complex changes were noted over time and showed an overall increase in the proportion of mosaic cells as age increased. Our large combined sample allowed for a unique ability to characterize detectable genetic mosaicism involving large structural events and strengthens the emerging evidence of non-random erosion of the genome in the aging population.