Evidence map›Paper›PMID 19917723›Full record

ArticleMolecular and cellular biology2010

Alternative mechanisms for coordinating polymerase alpha and MCM helicase.

Chanmi Lee, Ivan Liachko, Roxane Bouten, Zvi Kelman, Bik K Tye

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

29 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Four decades of Eukaryotic DNA replication: From yeast genetics to high-resolution cryo-EM structures of the replisome.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. MCM10: one tool for all-Integrity, maintenance and damage control.Seminars in cell & developmental biology · 2014
    Review
  19. Article
  20. Enigmatic roles of Mcm10 in DNA replication.Trends in biochemical sciences · 2013
    Review
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

5 authors at 2 institutions in 1 country.

Chanmi LeeDepartment of Molecular Biology & Genetics, Cornell University, Ithaca, New York 14853, USA.
Ivan Liachko
Roxane Bouten
Zvi Kelman
Bik K Tye
Cornell University · USBiotechnology Institute · US

Funding

Regulator of DNA Replication & Gene Expression in YeastR01GM072557 · NIGMS · CORNELL UNIVERSITY · PI TYE, BIK-KWOON · 2006 to 2009
$1.2M
NIGMS NIH HHS GM0722557NIGMS NIH HHS R01 GM072557
6 · The paper itself

Abstract

Functional coordination between DNA replication helicases and DNA polymerases at replication forks, achieved through physical linkages, has been demonstrated in prokaryotes but not in eukaryotes. In Saccharomyces cerevisiae, we showed that mutations that compromise the activity of the MCM helicase enhance the physical stability of DNA polymerase alpha in the absence of their presumed linker, Mcm10. Mcm10 is an essential DNA replication protein implicated in the stable assembly of the replisome by virtue of its interaction with the MCM2-7 helicase and Polalpha. Dominant mcm2 suppressors of mcm10 mutants restore viability by restoring the stability of Polalpha without restoring the stability of Mcm10, in a Mec1-dependent manner. In this process, the single-stranded DNA accumulation observed in the mcm10 mutant is suppressed. The activities of key checkpoint regulators known to be important for replication fork stabilization contribute to the efficiency of suppression. These results suggest that Mcm10 plays two important roles as a linker of the MCM helicase and Polalpha at the elongating replication fork--first, to coordinate the activities of these two molecular motors, and second, to ensure their physical stability and the integrity of the replication fork.

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA HelicasesDNA Polymerase IDNA ReplicationMinichromosome Maintenance ProteinsMutationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA HelicasesDNA Polymerase IMCM10 protein, S cerevisiaeMCM2 protein, S cerevisiaeMinichromosome Maintenance ProteinsPOL1 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID19917723
PMCPMC2798462
OpenAlexW2130717106

What OpenQuestion holds

Textmetadata
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.