期刊
CELL REPORTS
卷 7, 期 2, 页码 575-587出版社
CELL PRESS
DOI: 10.1016/j.celrep.2014.03.030
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资金
- Ligue contre le Cancer (Comite de Paris)
- Marie Curie IRG fellowship [PIRG07-GA-2010-268448]
- Association pour la Recherche contre le Cancer (ARC)
- Institut National du Cancer (INCa)
- Groupement des Entreprises Francaises dans la Lutte contre le Cancer (GEFLUC)
- Agence Nationale de la Recherche (ANR) [ANR-11-LABX-0071, ANR-11-IDEX-0005-01]
- Medical Research Council of South Africa
- National Research Foundation of South Africa
- National Basic Research Program [2012CB910702, 2011CB910802]
- National Natural Science Foundation Project [31125010, 81221004]
- INCa
- ANR
- ARC
Faithful DNA replication is essential for the maintenance of genome integrity. Incomplete genome replication leads to DNA breaks and chromosomal rearrangements, which are causal factors in cancer and other human diseases. Despite their importance, the molecular mechanisms that control human genome stability are incompletely understood. Here, we report a pathway that is required for human genome replication and stability. This pathway has three components: an E3 ubiquitin ligase, a transcriptional repressor, and a replication protein. The E3 ubiquitin ligase RBBP6 ubiquitinates and destabilizes the transcriptional repressor ZBTB38. This repressor negatively regulates transcription and levels of the MCM10 replication factor on chromatin. Cells lacking RBBP6 experience reduced replication fork progression and increased damage at common fragile sites due to ZBTB38 accumulation and MCM10 downregulation. Our results uncover a pathway that ensures genome-wide DNA replication and chromosomal stability.
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