Zscan4 regulates telomere elongation and genomic stability in ES cells

被引:344
作者
Zalzman, Michal [1 ]
Falco, Geppino [1 ]
Sharova, Lioudmila V. [1 ]
Nishiyama, Akira [1 ]
Thomas, Marshall [1 ]
Lee, Sung-Lim [1 ]
Stagg, Carole A. [1 ]
Hoang, Hien G. [1 ]
Yang, Hsih-Te [1 ]
Indig, Fred E. [2 ]
Wersto, Robert P. [2 ]
Ko, Minoru S. H. [1 ]
机构
[1] NIA, Dev Genom & Aging Sect, Genet Lab, Baltimore, MD 21224 USA
[2] NIA, Res Resources Branch, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
EMBRYONIC STEM-CELLS; DOUBLE-STRAND BREAKS; DNA; EXPRESSION; LENGTH; LINES; RECOMBINATION; MAINTENANCE; MICE; IDENTIFICATION;
D O I
10.1038/nature08882
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exceptional genomic stability is one of the hallmarks of mouse embryonic stem (ES) cells. However, the genes contributing to this stability remain obscure. We previously identified Zscan4 as a specific marker for two-cell embryo and ES cells. Here we show that Zscan4 is involved in telomere maintenance and long-term genomic stability in ES cells. Only 5% of ES cells express Zscan4 at a given time, but nearly all ES cells activate Zscan4 at least once during nine passages. The transient Zscan4-positive state is associated with rapid telomere extension by telomere recombination and upregulation of meiosis-specific homologous recombination genes, which encode proteins that are colocalized with ZSCAN4 on telomeres. Furthermore, Zscan4 knockdown shortens telomeres, increases karyotype abnormalities and spontaneous sister chromatid exchange, and slows down cell proliferation until reaching crisis by passage eight. Together, our data show a unique mode of genome maintenance in ES cells.
引用
收藏
页码:858 / U66
页数:8
相关论文
共 54 条
[1]   Defining Developmental Potency and Cell Lineage Trajectories by Expression Profiling of Differentiating Mouse Embryonic Stem Cells [J].
Aiba, Kazuhiro ;
Nedorezov, Timur ;
Piao, Yulan ;
Nishiyama, Akira ;
Matoba, Ryo ;
Sharova, Lioudmila V. ;
Sharov, Alexei A. ;
Yamanaka, Shinya ;
Niwa, Hitoshi ;
Ko, Minoru S. H. .
DNA RESEARCH, 2009, 16 (01) :73-80
[2]   Frequent recombination in telomeric DNA may extend the proliferative life of telomerase-negative cells [J].
Bailey, SM ;
Brenneman, MA ;
Goodwin, EH .
NUCLEIC ACIDS RESEARCH, 2004, 32 (12) :3743-3751
[3]   CO-FISH reveals inversions associated with isochromosome formation [J].
Bailey, SM ;
Goodwin, EH ;
Meyne, J ;
Cornforth, MN .
MUTAGENESIS, 1996, 11 (02) :139-144
[4]  
Blelloch RH, 2004, P NATL ACAD SCI USA, V101, P13985, DOI 10.1073/pnas.0405015101
[5]   Karyotypic stability, genotyping, differentiation, feeder-free maintenance, and gene expression sampling in three human embryonic stem cell lines derived prior to August 9, 2001 [J].
Brimble, SN ;
Zeng, XM ;
Weiler, DA ;
Luo, YQ ;
Liu, Y ;
Lyons, IG ;
Freed, WJ ;
Robins, AJ ;
Rao, MS ;
Schulz, TC .
STEM CELLS AND DEVELOPMENT, 2004, 13 (06) :585-597
[6]   TELOMERE ELONGATION IN IMMORTAL HUMAN-CELLS WITHOUT DETECTABLE TELOMERASE ACTIVITY [J].
BRYAN, TM ;
ENGLEZOU, A ;
GUPTA, J ;
BACCHETTI, S ;
REDDEL, RR .
EMBO JOURNAL, 1995, 14 (17) :4240-4248
[7]   Evidence for an alternative mechanism for maintaining telomere length in human tumors and tumor-derived cell lines [J].
Bryan, TM ;
Englezou, A ;
DallaPozza, L ;
Dunham, MA ;
Reddel, RR .
NATURE MEDICINE, 1997, 3 (11) :1271-1274
[8]  
Callicott RJ, 2006, COMPARATIVE MED, V56, P17
[9]   An in situ hybridzation-based screen for heterogeneously expressed genes in mouse ES cells [J].
Carter, Mark G. ;
Stagg, Carole A. ;
Falco, Geppino ;
Yoshikawa, Toshiyuki ;
Bassey, Uwem C. ;
Aiba, Kazuhiro ;
Sharova, Lioudmila V. ;
Shaik, Nabeebi ;
Ko, Minoru S. H. .
GENE EXPRESSION PATTERNS, 2008, 8 (03) :181-198
[10]   Telomere measurement by quantitative PCR [J].
Cawthon, RM .
NUCLEIC ACIDS RESEARCH, 2002, 30 (10) :e47