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Loss of Geminin induces rereplication in the presence of functional p53
M Melixetian, A Ballabeni, L Masiero, P Gasparini, R Zamponi, J Bartek, J Lukas, K Helin
Jazyk angličtina Země Spojené státy americké
NLK
Free Medical Journals
od 1962 do Před 6 měsíci
Freely Accessible Science Journals
od 1962 do Před 6 měsíci
PubMed Central
od 1962 do Před 6 měsíci
Europe PubMed Central
od 1962 do Před 6 měsíci
Open Access Digital Library
od 1955-01-25
Open Access Digital Library
od 1959-01-01
Open Access Digital Library
od 1962-01-01
PubMed
15159417
Knihovny.cz E-zdroje
- MeSH
- buněčná smrt genetika MeSH
- buněčné jádro genetika metabolismus MeSH
- buněčný cyklus * genetika MeSH
- CDC geny fyziologie MeSH
- DNA vazebné proteiny genetika metabolismus MeSH
- geminin MeSH
- histony genetika metabolismus MeSH
- jaderné proteiny genetika metabolismus MeSH
- lidé MeSH
- mitóza genetika MeSH
- nádorová transformace buněk genetika MeSH
- nádorové buněčné linie MeSH
- nádorový supresorový protein p53 genetika metabolismus MeSH
- nestabilita genomu * genetika MeSH
- polyploidie MeSH
- proteinkinasy genetika metabolismus MeSH
- proteiny buněčného cyklu genetika metabolismus MeSH
- rekombinasa Rad51 MeSH
- replikace DNA * genetika MeSH
- Check Tag
- lidé MeSH
Strict regulation of DNA replication is essential to ensure proper duplication and segregation of chromosomes during the cell cycle, as its deregulation can lead to genomic instability and cancer. Thus, eukaryotic organisms have evolved multiple mechanisms to restrict DNA replication to once per cell cycle. Here, we show that inactivation of Geminin, an inhibitor of origin licensing, leads to rereplication in human normal and tumor cells within the same cell cycle. We found a CHK1-dependent checkpoint to be activated in rereplicating cells accompanied by formation of gammaH2AX and RAD51 nuclear foci. Abrogation of the checkpoint leads to abortive mitosis and death of rereplicated cells. In addition, we demonstrate that the induction of rereplication is dependent on the replication initiation factors CDT1 and CDC6, and independent of the functional status of p53. These data show that Geminin is required for maintaining genomic stability in human cells.
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- $a Strict regulation of DNA replication is essential to ensure proper duplication and segregation of chromosomes during the cell cycle, as its deregulation can lead to genomic instability and cancer. Thus, eukaryotic organisms have evolved multiple mechanisms to restrict DNA replication to once per cell cycle. Here, we show that inactivation of Geminin, an inhibitor of origin licensing, leads to rereplication in human normal and tumor cells within the same cell cycle. We found a CHK1-dependent checkpoint to be activated in rereplicating cells accompanied by formation of gammaH2AX and RAD51 nuclear foci. Abrogation of the checkpoint leads to abortive mitosis and death of rereplicated cells. In addition, we demonstrate that the induction of rereplication is dependent on the replication initiation factors CDT1 and CDC6, and independent of the functional status of p53. These data show that Geminin is required for maintaining genomic stability in human cells.
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