Evidence map›Paper›PMID 27923055›Full record

ArticlePLoS genetics2016

A Novel Rrm3 Function in Restricting DNA Replication via an Orc5-Binding Domain Is Genetically Separable from Rrm3 Function as an ATPase/Helicase in Facilitating Fork Progression.

Salahuddin Syed, Claus Desler, Lene J Rasmussen, Kristina H Schmidt

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 17% of its field
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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  10. Role and Regulation of Pif1 Family Helicases at the Replication Fork.International journal of molecular sciences · 2022
    Review
  11. Article
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  16. Alterations in cellular metabolism triggered byProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Salahuddin SyedDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida, United States of America.
Claus DeslerCenter for Healthy Aging, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
Lene J RasmussenCenter for Healthy Aging, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
Kristina H SchmidtDepartment of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, Tampa, Florida, United States of America.
University of Copenhagen · DKUniversity of South Florida · US

Funding

Suppression of translocations by RecQ-like DNA helicasesR01GM081425 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI SCHMIDT, KRISTINA · 2008 to 2018
$2.6M
NIGMS NIH HHS R01 GM081425
6 · The paper itself

Abstract

In response to replication stress cells activate the intra-S checkpoint, induce DNA repair pathways, increase nucleotide levels, and inhibit origin firing. Here, we report that Rrm3 associates with a subset of replication origins and controls DNA synthesis during replication stress. The N-terminal domain required for control of DNA synthesis maps to residues 186-212 that are also critical for binding Orc5 of the origin recognition complex. Deletion of this domain is lethal to cells lacking the replication checkpoint mediator Mrc1 and leads to mutations upon exposure to the replication stressor hydroxyurea. This novel Rrm3 function is independent of its established role as an ATPase/helicase in facilitating replication fork progression through polymerase blocking obstacles. Using quantitative mass spectrometry and genetic analyses, we find that the homologous recombination factor Rdh54 and Rad5-dependent error-free DNA damage bypass act as independent mechanisms on DNA lesions that arise when Rrm3 catalytic activity is disrupted whereas these mechanisms are dispensable for DNA damage tolerance when the replication function is disrupted, indicating that the DNA lesions generated by the loss of each Rrm3 function are distinct. Although both lesion types activate the DNA-damage checkpoint, we find that the resultant increase in nucleotide levels is not sufficient for continued DNA synthesis under replication stress. Together, our findings suggest a role of Rrm3, via its Orc5-binding domain, in restricting DNA synthesis that is genetically and physically separable from its established catalytic role in facilitating fork progression through replication blocks.

Indexed as

Adenosine TriphosphatasesCell CycleCell Cycle ProteinsCell DivisionChromatinDNADNA-Binding ProteinsDNA DamageDNA HelicasesDNA ReplicationDNA TopoisomerasesOrigin Recognition ComplexPoint MutationReplication OriginSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsAdenosine TriphosphatasesCell Cycle ProteinsChromatinDNADNA-Binding ProteinsDNA HelicasesDNA TopoisomerasesMRC1 protein, S cerevisiaeORC5 protein, S cerevisiaeOrigin Recognition ComplexRAD5 protein, S cerevisiaeRDH54 protein, S cerevisiaeRrm3 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID27923055
PMCPMC5140057
OpenAlexW2559983447

What OpenQuestion holds

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Registered trials

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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.