Building a lineage from single cells: genetic techniques for cell lineage tracking

被引:178
作者
Woodworth, Mollie B. [1 ,2 ,3 ,4 ,5 ]
Girskis, Kelly M. [1 ,2 ,3 ,4 ,5 ]
Walsh, Christopher A. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Boston Childrens Hosp, Manton Ctr Orphan Dis, Div Genet & Gen, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
[5] Broad Inst MIT & Harvard, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
COPY-NUMBER VARIATION; GENOME AMPLIFICATION; CLONAL ANALYSIS; IN-VIVO; L1; RETROTRANSPOSITION; SEQUENCING ANALYSIS; SOMATIC MUTATIONS; TUMOR EVOLUTION; RADIAL GLIA; STEM-CELL;
D O I
10.1038/nrg.2016.159
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Resolving lineage relationships between cells in an organism is a fundamental interest of developmental biology. Furthermore, investigating lineage can drive understanding of pathological states, including cancer, as well as understanding of developmental pathways that are amenable to manipulation by directed differentiation. Although lineage tracking through the injection of retroviral libraries has long been the state of the art, a recent explosion of methodological advances in exogenous labelling and single-cell sequencing have enabled lineage tracking at larger scales, in more detail, and in a wider range of species than was previously considered possible. In this Review, we discuss these techniques for cell lineage tracking, with attention both to those that trace lineage forwards from experimental labelling, and those that trace backwards across the life history of an organism.
引用
收藏
页码:230 / 244
页数:15
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