Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/4097
Title: SMC proteins, new players in the maintenance of genomic stability
Keywords: Sister chromatid exchange
Double-strand break repair
Homologous Recombination
Break-induced replication
Collapsed replication forks
Cohesins
MRX/MRN complex
Smc5-Smc6
SMC complexes
Publisher: Landes Bioscience
Description: PMID: 17404505.-- Previously published online as a Cell Cycle E-publication: http://www.landesbioscience.com/journals/cc/abstract.php?id=4107
Homologous recombination (HR) is one of the key mechanisms responsible for the repair of DNA double-strand breaks (DSBs), including those that occur during DNA replication. Recent studies in yeast and mammals have uncovered that the SMC complexes cohesins and Smc5-Smc6 are recruited to induced DSBs, and play a role in the maintenance of genome stability by favouring SCR as the main recombinational DSB repair mechanism. These new results raise intriguing questions such as whether SMC proteins might play a functional role at collapsed replication forks, which may represent the main source of spontaneous recombinogenic damage. A deeper knowledge of the role of SMC proteins in DSB repair should contribute to a better understanding of chromosome dynamics and stability.
Peer reviewed
URI: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/4097
Other Identifiers: Cell Cycle 6(8): 914-918 (2007)
1538-4101 (Print)
1551-4005 (Online)
http://hdl.handle.net/10261/4097
10.4161/cc.6.8.4107
Appears in Collections:Digital Csic

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