Cellular barcoding: lineage tracing, screening and beyond

被引:133
作者
Kebschull, Justus M. [1 ,2 ]
Zador, Anthony M. [2 ]
机构
[1] Watson Sch Biol Sci, Cold Spring Harbor, NY USA
[2] Cold Spring Harbor Lab, POB 100, Cold Spring Harbor, NY 11724 USA
基金
美国国家卫生研究院;
关键词
SACCHAROMYCES-CEREVISIAE GENOME; HIGH-THROUGHPUT; CEREBRAL-CORTEX; IN-SITU; NEURONAL CLONES; SINGLE CELLS; CAENORHABDITIS-ELEGANS; FUNCTIONAL GENOMICS; RNA; DISPERSION;
D O I
10.1038/s41592-018-0185-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cellular barcoding is a technique in which individual cells are labeled with unique nucleic acid sequences, termed barcodes, so that they can be tracked through space and time. Cellular barcoding can be used to track millions of cells in parallel, and thus is an efficient approach for investigating heterogeneous populations of cells. Over the past 25 years, cellular barcoding has been used for fate mapping, lineage tracing and high-throughput screening, and has led to important insights into developmental biology and gene function. Driven by plummeting sequencing costs and the power of synthetic biology, barcoding is now expanding beyond traditional applications and into diverse fields such as neuroanatomy and the recording of cellular activity. In this review, we discuss the fundamental principles of cellular barcoding, including the underlying mathematics, and its applications in both new and established fields.
引用
收藏
页码:871 / 879
页数:9
相关论文
共 100 条
[1]   A Multiplexed Single-Cell CRISPR Screening Platform Enables Systematic Dissection of the Unfolded Protein Response [J].
Adamson, Britt ;
Norman, Thomas M. ;
Jost, Marco ;
Cho, Min Y. ;
Nunez, James K. ;
Chen, Yuwen ;
Villalta, Jacqueline E. ;
Gilbert, Luke A. ;
Horlbeck, Max A. ;
Hein, Marco Y. ;
Pak, Ryan A. ;
Gray, Andrew N. ;
Gross, Carol A. ;
Dixit, Atray ;
Parnas, Oren ;
Regev, Aviv ;
Weissman, Jonathan S. .
CELL, 2016, 167 (07) :1867-+
[2]   Whole-organism clone tracing using single-cell sequencing [J].
Alemany, Anna ;
Florescu, Maria ;
Baron, Chloe S. ;
Peterson-Maduro, Josi ;
van Oudenaarden, Alexander .
NATURE, 2018, 556 (7699) :108-+
[3]   A large-scale RNAi screen in human cells identifies new components of the p53 pathway [J].
Berns, K ;
Hijmans, EM ;
Mullenders, J ;
Brummelkamp, TR ;
Velds, A ;
Heimerikx, M ;
Kerkhoven, RM ;
Madiredjo, M ;
Nijkamp, W ;
Weigelt, B ;
Agami, R ;
Ge, W ;
Cavet, G ;
Linsley, PS ;
Beijersbergen, RL ;
Bernards, R .
NATURE, 2004, 428 (6981) :431-437
[4]   Studying clonal dynamics in response to cancer therapy using high-complexity barcoding [J].
Bhang, Hyo-eun C. ;
Ruddy, David A. ;
Radhakrishna, Viveksagar Krishnamurthy ;
Caushi, Justina X. ;
Zhao, Rui ;
Hims, Matthew M. ;
Singh, Angad P. ;
Kao, Iris ;
Rakiec, Daniel ;
Shaw, Pamela ;
Balak, Marissa ;
Raza, Alina ;
Ackley, Elizabeth ;
Keen, Nicholas ;
Schlabach, Michael R. ;
Palmer, Michael ;
Leary, Rebecca J. ;
Chiang, Derek Y. ;
Sellers, William R. ;
Michor, Franziska ;
Cooke, Vesselina G. ;
Korn, Joshua M. ;
Stegmeier, Frank .
NATURE MEDICINE, 2015, 21 (05) :440-U207
[5]  
Brenner S, 1995, US patent, Patent No. [US5763175A, 5763175A]
[6]  
Brenner S., 2007, WO patent application, Patent No. [WO2007087312A3, 2007087312A3]
[7]   Wiring specificity in the direction-selectivity circuit of the retina [J].
Briggman, Kevin L. ;
Helmstaedter, Moritz ;
Denk, Winfried .
NATURE, 2011, 471 (7337) :183-U67
[8]  
Cai D, 2013, NAT METHODS, V10, P540, DOI [10.1038/NMETH.2450, 10.1038/nmeth.2450]
[9]   A method for counting PCR template molecules with application to next-generation sequencing [J].
Casbon, James A. ;
Osborne, Robert J. ;
Brenner, Sydney ;
Lichtenstein, Conrad P. .
NUCLEIC ACIDS RESEARCH, 2011, 39 (12) :e81
[10]  
Chen X., 2018, BIORXIV