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Dynamics of leading-strand lesion skipping by the replisome.

Molecular cell (2013-11-26)
Joseph T P Yeeles, Kenneth J Marians
ZUSAMMENFASSUNG

The E. coli replisome stalls transiently when it encounters a lesion in the leading-strand template, skipping over the damage by reinitiating replication at a new primer synthesized downstream by the primase. We report here that template unwinding and lagging-strand synthesis continue downstream of the lesion at a reduced rate after replisome stalling, that one replisome is capable of skipping multiple lesions, and that the rate-limiting steps of replication restart involve the synthesis and activation of the new primer downstream. We also find little support for the concept that polymerase uncoupling, where extensive lagging-strand synthesis proceeds downstream in the absence of leading-strand synthesis, involves physical separation of the leading-strand polymerase from the replisome. Instead, our data indicate that extensive uncoupled replication likely results from a failure of the leading-strand polymerase still associated with the DNA helicase and the lagging-strand polymerase that are proceeding downstream to reinitiate synthesis.

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Taq-DNA-Polymerase aus Thermus aquaticus, with 10× PCR reaction buffer containing MgCl2
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Taq-DNA-Polymerase aus Thermus aquaticus, with 10× PCR reaction buffer without MgCl2
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DNA-Polymerase I, Klenow-Fragment aus E. coli, buffered aqueous glycerol solution
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DNA-Polymerase I aus E. coli lysogen für NM 964, buffered aqueous glycerol solution