Mosaicism in health and disease - clones picking up speed

被引:197
作者
Forsberg, Lars A. [1 ,2 ]
Gisselsson, David [3 ,4 ]
Dumanski, Jan P. [1 ,2 ]
机构
[1] Uppsala Univ, Dept Immunol Genet & Pathol, SE-75108 Uppsala, Sweden
[2] Uppsala Univ, Sci Life Lab, SE-75108 Uppsala, Sweden
[3] Lund Univ, Skane Reg & Univ Labs, Dept Clin Genet, SE-22184 Lund, Sweden
[4] Lund Univ, Skane Reg & Univ Labs, Dept Oncol Pathol, SE-22184 Lund, Sweden
基金
瑞典研究理事会; 欧洲研究理事会;
关键词
Y-CHROMOSOME LOSS; COPY-NUMBER-VARIATION; CONFINED PLACENTAL MOSAICISM; TURNER-SYNDROME; SOMATIC MOSAICISM; PERIPHERAL-BLOOD; L1; RETROTRANSPOSITION; UNIPARENTAL DISOMY; CLINICAL-SIGNIFICANCE; FETAL MICROCHIMERISM;
D O I
10.1038/nrg.2016.145
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Post-zygotic variation refers to genetic changes that arise in the soma of an individual and that are not usually inherited by the next generation. Although there is a paucity of research on such variation, emerging studies show that it is common: individuals are complex mosaics of genetically distinct cells, to such an extent that no two somatic cells are likely to have the exact same genome. Although most types of mutation can be involved in post-zygotic variation, structural genetic variants are likely to leave the largest genomic footprint. Somatic variation has diverse physiological roles and pathological consequences, particularly when acquired variants influence the clonal trajectories of the affected cells. Post-zygotic variation is an important confounder in medical genetic testing and a promising avenue for research: future studies could involve analyses of sorted and single cells from multiple tissue types to fully explore its potential.
引用
收藏
页码:128 / 142
页数:15
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