How to count chromosomes in a cell: An overview of current and novel technologies

被引:35
作者
Bakker, Bjorn [1 ]
van den Bos, Hilda [1 ]
Lansdorp, Peter M. [1 ]
Foijer, Floris [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, European Res Inst Biol Ageing ERIBA, Groningen, Netherlands
关键词
aneuploidy; chromosomal instability; karyotyping; next generation sequencing; COPY-NUMBER VARIATION; COMPARATIVE GENOMIC HYBRIDIZATION; SINGLE-CELL; MOLECULAR CYTOGENETICS; ALZHEIMERS-DISEASE; HUMAN BRAIN; ANEUPLOIDY; CANCER; INSTABILITY; DNA;
D O I
10.1002/bies.201400218
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aneuploidy, an aberrant number of chromosomes in a cell, is a feature of several syndromes associated with cognitive and developmental defects. In addition, aneuploidy is considered a hallmark of cancer cells and has been suggested to play a role in neurodegenerative disease. To better understand the relationship between aneuploidy and disease, various methods to measure the chromosome numbers in cells have been developed, each with their own advantages and limitations. While some methods rely on dividing cells and thus bias aneuploidy rates to that population, other, more unbiased methods can only detect the average aneuploidy rates in a cell population, cloaking cell-to-cell heterogeneity. Furthermore, some techniques are more prone to technical artefacts, which can result in over- or underestimation of aneuploidy rates. In this review, we provide an overview of several traditional karyotyping methods as well as the latest high throughput next generation sequencing karyotyping protocols with their respective advantages and disadvantages.
引用
收藏
页码:570 / 577
页数:8
相关论文
共 78 条
[1]  
Bayani Jane, 2004, Curr Protoc Cell Biol, VChapter 22, DOI 10.1002/0471143030.cb2204s23
[2]   Applications of SKY in cancer cytogenetics [J].
Bayani, JM ;
Squire, JA .
CANCER INVESTIGATION, 2002, 20 (03) :373-386
[3]   High-resolution analysis of DNA copy number using oligonucleotide microarrays [J].
Bignell, GR ;
Huang, J ;
Greshock, J ;
Watt, S ;
Butler, A ;
West, S ;
Grigorova, M ;
Jones, KW ;
Wei, W ;
Stratton, MR ;
Futreal, PA ;
Weber, B ;
Shapero, MH ;
Wooster, R .
GENOME RESEARCH, 2004, 14 (02) :287-295
[4]   Hansemann, Boveri, chromosomes and the gametogenesis-related theories of tumours [J].
Bignold, Leon P. ;
Coghlan, Brian L. D. ;
Jersmann, Hubertus Pa. .
CELL BIOLOGY INTERNATIONAL, 2006, 30 (07) :640-644
[5]  
Boveri T, 1995, TRENDS CELL BIOL, V5, P384
[6]   Genomic microarrays: a technology overview [J].
Brady, Paul D. ;
Vermeesch, Joris R. .
PRENATAL DIAGNOSIS, 2012, 32 (04) :336-343
[7]   Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain [J].
Cai, Xuyu ;
Evrony, Gilad D. ;
Lehmann, Hillel S. ;
Elhosary, Princess C. ;
Mehta, Bhaven K. ;
Poduri, Annapurna ;
Walsh, Christopher A. .
CELL REPORTS, 2014, 8 (05) :1280-1289
[8]   Single-cell copy number variation detection [J].
Cheng, Jiqiu ;
Vanneste, Evelyne ;
Konings, Peter ;
Voet, Thierry ;
Vermeesch, Joris R. ;
Moreau, Yves .
GENOME BIOLOGY, 2011, 12 (08)
[9]   Molecular cytogenetics: recent developments and applications in cancer [J].
Das, K. ;
Tan, P. .
CLINICAL GENETICS, 2013, 84 (04) :315-325
[10]   Comprehensive human genome amplification using multiple displacement amplification [J].
Dean, FB ;
Hosono, S ;
Fang, LH ;
Wu, XH ;
Faruqi, AF ;
Bray-Ward, P ;
Sun, ZY ;
Zong, QL ;
Du, YF ;
Du, J ;
Driscoll, M ;
Song, WM ;
Kingsmore, SF ;
Egholm, M ;
Lasken, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) :5261-5266