Author
Listed:
- Bo Sun
(Cornell University
Cornell University
ShanghaiTech University)
- Anupam Singh
(Robert Wood Johnson Medical School, Rutgers University)
- Shemaila Sultana
(Robert Wood Johnson Medical School, Rutgers University)
- James T. Inman
(Cornell University
Cornell University)
- Smita S. Patel
(Robert Wood Johnson Medical School, Rutgers University)
- Michelle D. Wang
(Cornell University
Cornell University)
Abstract
To ensure accurate DNA replication, a replisome must effectively overcome numerous obstacles on its DNA substrate. After encountering an obstacle, a progressing replisome often aborts DNA synthesis but continues to unwind. However, little is known about how DNA synthesis is resumed downstream of an obstacle. Here, we examine the consequences of a non-replicating replisome collision with a co-directional RNA polymerase (RNAP). Using single-molecule and ensemble methods, we find that T7 helicase interacts strongly with a non-replicating T7 DNA polymerase (DNAP) at a replication fork. As the helicase advances, the associated DNAP also moves forward. The presence of the DNAP increases both helicase’s processivity and unwinding rate. We show that such a DNAP, together with its helicase, is indeed able to actively disrupt a stalled transcription elongation complex, and then initiates replication using the RNA transcript as a primer. These observations exhibit T7 helicase’s novel role in replication re-initiation.
Suggested Citation
Bo Sun & Anupam Singh & Shemaila Sultana & James T. Inman & Smita S. Patel & Michelle D. Wang, 2018.
"Helicase promotes replication re-initiation from an RNA transcript,"
Nature Communications, Nature, vol. 9(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04702-x
DOI: 10.1038/s41467-018-04702-x
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