Evidence map›Paper›PMID 38585807›Full record

ArticlebioRxiv : the preprint server for biology2024

Single-Molecule Imaging Reveals the Mechanism of Bidirectional Replication Initiation in Metazoa.

Riki Terui, Scott Berger, Larissa Sambel, Dan Song, Gheorghe Chistol

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Riki TeruiChemical and Systems Biology, Stanford School of Medicine, Stanford CA94305.ORCID 0000-0002-9795-4139
Scott BergerBiophysics Program, Stanford School of Medicine, Stanford CA94305.ORCID 0000-0003-3219-2310
Larissa SambelChemical and Systems Biology, Stanford School of Medicine, Stanford CA94305.ORCID 0000-0002-9437-944X
Dan SongCurrent Address: Eikon Therapeutics Inc.
Gheorghe ChistolChemical and Systems Biology, Stanford School of Medicine, Stanford CA94305.ORCID 0000-0003-4868-3667
Stanford Medicine · USHeron Therapeutics (United States) · US

Funding

Structure-Function Analysis of DNA Replication Initiation Factors Implicated in DiseaseR35GM147060 · NIGMS · STANFORD UNIVERSITY · PI Gheorghe Chistol · 2022 to 2026
$2.2M
NIGMS NIH HHS R35 GM147060
6 · The paper itself

Abstract

Metazoan genomes are copied bidirectionally from thousands of replication origins. Replication initiation entails the assembly and activation of two CMG (Cdc45•Mcm2-7•GINS) helicases at each origin. This requires several firing factors (including TopBP1, RecQL4, DONSON) whose exact roles remain unclear. How two helicases are correctly assembled and activated at every single origin is a long-standing question. By visualizing the recruitment of GINS, Cdc45, TopBP1, RecQL4, and DONSON in real time, we uncovered a surprisingly dynamic picture of initiation. Firing factors transiently bind origins but do not travel with replisomes. Two Cdc45 simultaneously arrive at each origin and two GINS are recruited together, even though neither protein can dimerize. The synchronized delivery of two GINS is mediated by DONSON, which acts as a dimerization scaffold. We show that RecQL4 promotes DONSON dissociation and facilitates helicase activation. The high fidelity of bidirectional origin firing can be explained by a Hopfield-style kinetic proofreading mechanism.

Identifiers

PMID38585807
PMCPMC10996697
OpenAlexW4393315770

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.