Unknown

Dataset Information

0

Structures and operating principles of the replisome.


ABSTRACT: Visualization in atomic detail of the replisome that performs concerted leading- and lagging-DNA strand synthesis at a replication fork has not been reported. Using bacteriophage T7 as a model system, we determined cryo-electron microscopy structures up to 3.2-angstroms resolution of helicase translocating along DNA and of helicase-polymerase-primase complexes engaging in synthesis of both DNA strands. Each domain of the spiral-shaped hexameric helicase translocates sequentially hand-over-hand along a single-stranded DNA coil, akin to the way AAA+ ATPases (adenosine triphosphatases) unfold peptides. Two lagging-strand polymerases are attached to the primase, ready for Okazaki fragment synthesis in tandem. A ? hairpin from the leading-strand polymerase separates two parental DNA strands into a T-shaped fork, thus enabling the closely coupled helicase to advance perpendicular to the downstream DNA duplex. These structures reveal the molecular organization and operating principles of a replisome.

SUBMITTER: Gao Y 

PROVIDER: S-EPMC6681829 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Structures and operating principles of the replisome.

Gao Yang Y   Cui Yanxiang Y   Fox Tara T   Lin Shiqiang S   Wang Huaibin H   de Val Natalia N   Zhou Z Hong ZH   Yang Wei W  

Science (New York, N.Y.) 20190124 6429


Visualization in atomic detail of the replisome that performs concerted leading- and lagging-DNA strand synthesis at a replication fork has not been reported. Using bacteriophage T7 as a model system, we determined cryo-electron microscopy structures up to 3.2-angstroms resolution of helicase translocating along DNA and of helicase-polymerase-primase complexes engaging in synthesis of both DNA strands. Each domain of the spiral-shaped hexameric helicase translocates sequentially hand-over-hand a  ...[more]

Similar Datasets

| S-EPMC2667182 | biostudies-literature
| S-EPMC3705962 | biostudies-literature
2023-07-06 | GSE218307 | GEO
2023-07-07 | GSE218306 | GEO
2023-07-07 | GSE218305 | GEO
| S-EPMC5466818 | biostudies-literature
2023-07-07 | GSE218304 | GEO
| S-EPMC6000178 | biostudies-literature
| S-EPMC6294490 | biostudies-literature
2017-03-07 | GSE80280 | GEO