Article ID Journal Published Year Pages File Type
1998095 Molecular Cell 2006 6 Pages PDF
Abstract

As the replication fork progresses, synthesis of the discontinuous lagging strand requires frequent priming and cycling of the lagging strand polymerase to the new primers. It appears that this mechanism also permits bypass of template lesions on both strands, leaving the damage behind in a single-strand gap and precluding fork stalling or collapse.

Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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