Evidence map›Paper›PMID 24300032›Full record

ArticleCell cycle (Georgetown, Tex.)2014

The tail that wags the dog: p12, the smallest subunit of DNA polymerase δ, is degraded by ubiquitin ligases in response to DNA damage and during cell cycle progression.

Marietta Y W T Lee, Sufang Zhang, Szu Hua Sharon Lin, Xiaoxiao Wang, Zbigniew Darzynkiewicz, Zhongtao Zhang, Ernest Y C Lee

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

28 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Canonical binding ofFrontiers in molecular biosciences · 2023
    Article
  9. Beyond the Lesion: Back to High Fidelity DNA Synthesis.Frontiers in molecular biosciences · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Models of Replicator Proliferation Involving Differential Replicator Subunit Stability.Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life · 2018
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Marietta Y W T LeeDepartment of Biochemistry and Molecular Biology; New York Medical College; Valhalla, NY USA.
Sufang ZhangDepartment of Biochemistry and Molecular Biology; New York Medical College; Valhalla, NY USA.
Szu Hua Sharon LinDepartment of Biochemistry and Molecular Biology; New York Medical College; Valhalla, NY USA.
Xiaoxiao WangDepartment of Biochemistry and Molecular Biology; New York Medical College; Valhalla, NY USA.
Zbigniew DarzynkiewiczDepartment of Pathology; Brander Cancer Research Institute; New York Medical College; Valhalla, NY USA.
Zhongtao ZhangDepartment of Biochemistry and Molecular Biology; New York Medical College; Valhalla, NY USA.
Ernest Y C LeeDepartment of Biochemistry and Molecular Biology; New York Medical College; Valhalla, NY USA.
Catalyst Foundation · USNew York Medical College · US

Funding

BIOCHEMICAL STUDIES OF POLYMERASE DELTAR01GM031973 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LEE, MARIETTA Y. · 1985 to 2012
$5.8M
Modification of DNA Polymerase Delta by a Novel Mechanism During Replication StreR01ES014737 · NIEHS · NEW YORK MEDICAL COLLEGE · PI LEE, MARIETTA Y., ZHANG, ZHONGTAO · 2008 to 2017
$3.5M
NIEHS NIH HHS ES14737NIEHS NIH HHS R01 ES014737NIGMS NIH HHS GM31973NIGMS NIH HHS R01 GM031973
6 · The paper itself

Abstract

DNA polymerase δ (Pol δ) is a key enzyme in eukaryotic DNA replication. Human Pol δ is a heterotetramer whose p12 subunit is degraded in response to DNA damage, leading to the in vivo conversion of Pol δ4 to Pol δ3. Two E3 ubiquitin ligases, RNF8 and CRL4(Cdt2), participate in the DNA damage-induced degradation of p12. We discuss how these E3 ligases integrate the formation of Pol δ3 and ubiquitinated PCNA for DNA repair processes. CRL4(Cdt2) partially degrades p12 during normal cell cycle progression, thereby generating Pol δ3 during S phase. This novel finding extends the current view of the role of Pol δ3 in DNA repair and leads to the hypothesis that it participates in DNA replication. The coordinated regulation of licensing factors and Pol δ3 by CRL4(Cdt2) now opens new avenues for control of DNA replication. A parallel study of Pol δ4 and Pol δ3 in Okazaki fragment processing provides evidence for a role of Pol δ3 in DNA replication. We discuss several new perspectives of the role of the 2 forms of Pol δ in DNA replication and repair, as well the significance of the integration of p12 regulation in DNA repair and cell cycle progression.

Indexed as

Cell CycleDNADNA DamageDNA Polymerase IIIDNA RepairDNA ReplicationHeLa CellsHumansProtein SubunitsProteolysisUbiquitinUbiquitin-Protein LigasesDNADNA Polymerase IIIOkazaki fragmentsPOLD4 protein, humanProtein SubunitsUbiquitinUbiquitin-Protein Ligasescell cyclecell cycle progressionCRL4Cdt2DNA damageDNA polymerase δDNA replicationp12 subunitRNF8

Identifiers

PMID24300032
PMCPMC3925730
OpenAlexW2001237591

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.