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Hereditas(Beijing) ›› 2018, Vol. 40 ›› Issue (8): 620-631.doi: 10.16288/j.yczz.18-091

• Reviews • Previous Articles     Next Articles

Comparison of different single cell whole genome amplification methods and MALBAC applications in assisted reproduction

Yaxin Yao1,Yongfu La2,Ran Di1,Qiuyue Liu1,Wenping Hu1,Xiangyu Wang1,Mingxing Chu1()   

  1. 1. Key Laboratory of Animal Genetics, Breeding and Reproduction of Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China
    2. College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China
  • Received:2018-04-07 Revised:2018-06-09 Online:2018-08-16 Published:2018-07-02
  • Contact: Chu Mingxing E-mail:mxchu@263.net
  • Supported by:
    Supported by the National Natural Science Foundation of China(31772580);Supported by the National Natural Science Foundation of China(31472078);Earmarked Fund for China Agriculture Research System(CARS-38);Central Public-interest Scientific Institution Basal Research Fund(Y2017JC24);Agricultural Science and Technology Innovation Program of China(ASTIP-IAS13);China Agricultural Scientific Research Outstanding Talents and Their Innovative Teams Program, China High-level Talents Special Support Plan Scientific and Technological Innovation Leading Talents Program

Abstract:

Single-cell whole genome amplification (WGA) is a new technology, which can amplify small amounts of DNA from single cell and obtain the high coverage whole genome DNA template for revealing cell heterogeneity. Single cell WGA methods mainly include primer extension preamplification PCR (PEP-PCR), degenerate oligonucleotide primed PCR (DOP-PCR), multiple displacement amplification (MDA), and multiple annealing and looping-based amplification cycles (MALBAC). In this review, we describe the principles and applications of different single cell genome wide amplification, and we evaluate and compare their amplification efficiency, including the coverage of genome, homogeneity, reproducibility, and detection power of single-nucleotide variants (SNV) and copy number variants (CNV). The results show that MALBAC have the highest amplification homogeneity, the lowest allelic gene knockdown rate, the best reproducibility, and the best detection effect on CNV and SNV. We also describe the applications of MALBAC in human single sperm meiosis, aneuploidy analysis, and human oocyte genome research.

Key words: single cell whole genome amplification, MALBAC, DOP-PCR, MDA, single cell