TY - JOUR
T1 - Timing, coordination, and rhythm: Acrobatics at the DNA replication fork
AU - Hamdan, Samir
AU - Van Oijen, Antoine M.
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2010/4/9
Y1 - 2010/4/9
N2 - In DNA replication, the antiparallel nature of the parental duplex imposes certain constraints on the activity of the DNA polymerases that synthesize new DNA. The leading-strand polymerase advances in a continuous fashion, but the lagging-strand polymerase is forced to restart at short intervals. In several prokaryotic systems studied so far, this problem is solved by the formation of a loop in the lagging strand of the replication fork to reorient the lagging-strand DNA polymerase so that it advances in parallel with the leading-strand polymerase. The replication loop grows and shrinks during each cycle of Okazaki fragment synthesis. The timing of Okazaki fragment synthesis and loop formation is determined by a subtle interplay of enzymatic activities at the fork. Recent developments in single-molecule techniques have enabled the direct observation of these processes and have greatly contributed to a better understanding of the dynamic nature of the replication fork. Here, we will review recent experimental advances, present the current models, and discuss some of the exciting developments in the field. 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
AB - In DNA replication, the antiparallel nature of the parental duplex imposes certain constraints on the activity of the DNA polymerases that synthesize new DNA. The leading-strand polymerase advances in a continuous fashion, but the lagging-strand polymerase is forced to restart at short intervals. In several prokaryotic systems studied so far, this problem is solved by the formation of a loop in the lagging strand of the replication fork to reorient the lagging-strand DNA polymerase so that it advances in parallel with the leading-strand polymerase. The replication loop grows and shrinks during each cycle of Okazaki fragment synthesis. The timing of Okazaki fragment synthesis and loop formation is determined by a subtle interplay of enzymatic activities at the fork. Recent developments in single-molecule techniques have enabled the direct observation of these processes and have greatly contributed to a better understanding of the dynamic nature of the replication fork. Here, we will review recent experimental advances, present the current models, and discuss some of the exciting developments in the field. 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
UR - http://hdl.handle.net/10754/334568
UR - http://www.jbc.org/lookup/doi/10.1074/jbc.R109.022939
UR - http://www.scopus.com/inward/record.url?scp=77953489802&partnerID=8YFLogxK
U2 - 10.1074/jbc.R109.022939
DO - 10.1074/jbc.R109.022939
M3 - Article
C2 - 20382733
SN - 0021-9258
VL - 285
SP - 18979
EP - 18983
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 25
ER -