Chromosome dynamic changes in two cultured chinese human embryonic stem cell lines: Single nucleotide polymorphism, copy number variation and loss of heterozygosity

被引:7
作者
Chen, Xue-Mei [1 ,2 ]
Kan, Quan-Cheng
Wang, Fang [1 ]
Kong, Hui-Juan [1 ]
Zhang, Yong-Yong [1 ]
Yu, Wen-Zhu [1 ]
Sun, Ying-Pu [1 ]
机构
[1] Zhengzhou Univ, Reprod Med Ctr, Affiliated Hosp 1, Zhengzhou 450052, Peoples R China
[2] Zhengzhou Univ, Dept Human Anat, Coll Basic Med Sci, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
HUMAN EMBRYONIC STEM CELLS; COPY NUMBER VARIATION; SINGLE NUCLEOTIDE POLYMORPHISM; LOSS OF HETEROZYGOSITY; KARYOTYPE; IN-VITRO CULTURE; TUMORS; AMPLIFICATION; HYBRIDIZATION; INTEGRITY; REVEALS; GENES;
D O I
10.1002/jcb.24229
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
The quality and safety of human embryonic stem cells (hESCs) in clinical application depend on gene stability. Two Chinese hESC lines, Zh1 and Zh21, were incubated over a long period. We observed and compared the gene stability in the passage numbers 20, 17 for Zh1 cell line and passage numbers 27, 60, 68 for Zh21 cell line. Single nucleotide polymorphisis analysis indicated that hESCs in early passages had relative gene stability; and with the increase in passage number, gene instability became strong. We also found that there were copy number variations (CNVs) in both Zh21 and Zh1. We analyzed the CNVs of Chinese Han Beijing man (CHB; normal Chinese people) and found that the all CNV forms were the loss in Zh21, Zh1, and CHB. We also analyzed and compared the related pathways of the mutant genes. We propose three steps to ensure hESC safety. Firstly, besides the conventional methods such as pluripotent genes, chromosome G-banding and teratoma, high-resolution DNA chip analysis should also be adopted; secondly, chromosomal properties are monitored every 10 passages in less than passage 50 and every 5 passages in more than passage 50; thirdly, the related pathways of mutant genes should be observed because only the mutant genes with variations of their related pathways may affected cell functions. J. Cell. Biochem. 113: 35203527, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:3520 / 3527
页数:8
相关论文
共 30 条
  • [11] Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivation
    Inzunza, J
    Sahlén, S
    Holmberg, K
    Strömberg, AM
    Teerijoki, H
    Blennow, E
    Hovatta, O
    Malmgren, H
    [J]. MOLECULAR HUMAN REPRODUCTION, 2004, 10 (06) : 461 - 466
  • [12] Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
    Kumar, Prateek
    Henikoff, Steven
    Ng, Pauline C.
    [J]. NATURE PROTOCOLS, 2009, 4 (07) : 1073 - 1082
  • [13] Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human ESCs and iPSCs during Reprogramming and Time in Culture
    Laurent, Louise C.
    Ulitsky, Igor
    Slavin, Ileana
    Tran, Ha
    Schork, Andrew
    Morey, Robert
    Lynch, Candace
    Harness, Julie V.
    Lee, Sunray
    Barrero, Maria J.
    Ku, Sherman
    Martynova, Marina
    Semechkin, Ruslan
    Galat, Vasiliy
    Gottesfeld, Joel
    Belmonte, Juan Carlos Izpisua
    Murry, Chuck
    Keirstead, Hans S.
    Park, Hyun-Sook
    Schmidt, Uli
    Laslett, Andrew L.
    Muller, Franz-Josef
    Nievergelt, Caroline M.
    Shamir, Ron
    Loring, Jeanne F.
    [J]. CELL STEM CELL, 2011, 8 (01) : 106 - 118
  • [14] Establishment of polycystic ovary syndrome-derived human embryonic stem cell lines
    Li, Peng-fen
    Wang, Fang
    Kong, Hui-juan
    Zhao, Fang
    Bai, Ai-hong
    Chen, Xue-mei
    Sun, Ying-pu
    [J]. GYNECOLOGICAL ENDOCRINOLOGY, 2012, 28 (01) : 25 - 28
  • [15] Genomic alterations in cultured human embryonic stem cells
    Maitra, A
    Arking, DE
    Shivapurkar, N
    Ikeda, M
    Stastny, V
    Kassauei, K
    Sui, GP
    Cutler, DJ
    Liu, Y
    Brimble, SN
    Noaksson, K
    Hyllner, J
    Schulz, TC
    Zeng, XM
    Freed, WJ
    Crook, J
    Abraham, S
    Colman, A
    Sartipy, P
    Matsui, SI
    Carpenter, M
    Gazdar, AF
    Rao, M
    Chakravarti, A
    [J]. NATURE GENETICS, 2005, 37 (10) : 1099 - 1103
  • [16] Identification and Classification of Chromosomal Aberrations in Human Induced Pluripotent Stem Cells
    Mayshar, Yoav
    Ben-David, Uri
    Lavon, Neta
    Biancotti, Juan-Carlos
    Yakir, Benjamin
    Clark, Amander T.
    Plath, Kathrin
    Lowry, William E.
    Benvenisty, Nissim
    [J]. CELL STEM CELL, 2010, 7 (04) : 521 - 531
  • [17] Preserving the genetic integrity of human embryonic stem cells
    Mitalipova, MM
    Rao, RR
    Hoyer, DM
    Johnson, JA
    Meisner, LF
    Jones, KL
    Dalton, S
    Stice, SL
    [J]. NATURE BIOTECHNOLOGY, 2005, 23 (01) : 19 - 20
  • [18] An Improved Technique for Chromosomal Analysis of Human ES and iPS Cells
    Moralli, Daniela
    Yusuf, Mohammed
    Mandegar, Mohammad A.
    Khoja, Suhail
    Monaco, Zoia L.
    Volpi, Emanuela V.
    [J]. STEM CELL REVIEWS AND REPORTS, 2011, 7 (02) : 471 - 477
  • [19] High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity
    Narva, Elisa
    Autio, Reija
    Rahkonen, Nelly
    Kong, Lingjia
    Harrison, Neil
    Kitsberg, Danny
    Borghese, Lodovica
    Itskovitz-Eldor, Joseph
    Rasool, Omid
    Dvorak, Petr
    Hovatta, Outi
    Otonkoski, Timo
    Tuuri, Timo
    Cui, Wei
    Brustle, Oliver
    Baker, Duncan
    Maltby, Edna
    Moore, Harry D.
    Benvenisty, Nissim
    Andrews, Peter W.
    Yli-Harja, Olli
    Lahesmaa, Riitta
    [J]. NATURE BIOTECHNOLOGY, 2010, 28 (04) : 371 - U103
  • [20] Restricted 12p amplification and RAS mutation in human germ cell tumors of the adult testis
    Roelofs, H
    Mostert, MC
    Pompe, K
    Zafarana, G
    van Oorschot, M
    van Gurp, RJHLM
    Gillis, AJM
    Stoop, H
    Beverloo, B
    Oosterhuis, JW
    Bokemeyer, C
    Looijenga, LHJ
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (04) : 1155 - 1166