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Zscan4 regulates telomere elongation and genomic stability in ES cellsopen access

Authors
Zalzman, M.Falco, G.Sharova, L.V.Nishiyama, A.Thomas, M.Lee, S.-L.Stagg, C.A.Hoang, H.G.Yang, H.-T.Indig, F.E.Wersto, R.P.Ko, M.S.H.
Issue Date
2010
Citation
Nature, v.464, no.7290, pp 858 - 863
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
Nature
Volume
464
Number
7290
Start Page
858
End Page
863
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/25994
DOI
10.1038/nature08882
ISSN
0028-0836
1476-4687
Abstract
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. ? 2010 Macmillan Publishers Limited. All rights reserved.
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