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Dynamic look at DNA unwinding by a replicative helicase
Author(s) -
SeungJae Lee,
Salman Syed,
Eric J. Enemark,
Stephen Schuck,
Arne Stenlund,
Taekjip Ha,
Leemor JoshuaTor
Publication year - 2014
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1322254111
Subject(s) - helicase , minichromosome maintenance , dna replication , control of chromosome duplication , biology , rna helicase a , replication protein a , dna , primase , genetics , dnab helicase , microbiology and biotechnology , replisome , origin recognition complex , computational biology , eukaryotic dna replication , dna binding protein , gene , transcription factor , rna , reverse transcriptase
A prerequisite for DNA replication is the unwinding of duplex DNA catalyzed by a replicative hexameric helicase. Despite a growing body of research, key elements of helicase mechanism remain under substantial debate. In particular, the number of DNA strands encircled by the helicase ring during unwinding and the ring orientation at the replication fork completely contrast in contemporary mechanistic models. Here we use single-molecule and ensemble assays to address these questions for the papillomavirus E1 helicase. We find that E1 unwinds DNA with a strand-exclusion mechanism, with the N-terminal side of the helicase ring facing the replication fork. We show that E1 generates strikingly heterogeneous unwinding patterns stemming from varying degrees of repetitive movements, which is modulated by the DNA-binding domain. Together, our studies reveal previously unrecognized dynamic facets of replicative helicase unwinding mechanisms.

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