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Record W2620071155 · doi:10.18632/oncotarget.18070

Lysine methylation of FEN1 by SET7 is essential for its cellular response to replicative stress

2017· article· en· W2620071155 on OpenAlexafffundabout
Palaniraja Thandapani, Anthony M. Couturier, Zhenbao Yu, Xing Li, Jean‐François Couture, Shawn Li, Jean‐Yves Masson, Stéphane Richard

Bibliographic record

VenueOncotarget · 2017
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicEpigenetics and DNA Methylation
Canadian institutionsWestern UniversityUniversity of OttawaUniversité LavalMcGill UniversityJewish General Hospital
FundersFonds de Recherche du Québec - SantéHealth Canada
KeywordsMethylationDNA repairBiologyOkazaki fragmentsMethyltransferaseDNA replicationHistoneDNA damageHistone methyltransferaseDNA methylationCell biologyHistone H4Molecular biologyBiochemistryDNAEukaryotic DNA replicationGene expression

Abstract

fetched live from OpenAlex

// Palaniraja Thandapani 1,2,* , Anthony M. Couturier 3,* , Zhenbao Yu 1,2 , Xing Li 4 , Jean-François Couture 5 , Shawn Li 3 , Jean-Yves Masson 3 and Stéphane Richard 1,2 1 Terry Fox Molecular Oncology Group and Bloomfield Center for Research on Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Québec, Canada 2 Departments of Oncology and Medicine, McGill University, Montréal, Québec, Canada 3 Genome Stability Laboratory, Laval University Cancer Research Center, CRCHU de Québec, Québec, Canada 4 Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada 5 Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, Ontario, Canada * These authors have contributed equally to this work Correspondence to: Jean-Yves Masson, email: // Stéphane Richard, email: // Keywords : lysine methylation, SET7, FEN1, DNA damage response, DNA replication Received : April 12, 2017 Accepted : April 18, 2017 Published : May 22, 2017 Abstract The DNA damage response (DDR) is central to the cell survival and it requires post-translational modifications, in part, to sense the damage, amplify the signaling response and recruit and regulate DNA repair enzymes. Lysine methylation of histones such as H4K20 and non-histone proteins including p53 has been shown to be essential for the mounting of the DDR. It is well-known that the lysine methyltransferase SET7 regulates the DDR, as cells lacking this enzyme are hypersensitive to chemotherapeutic drugs. To define addition substrates of SET7 involved in the DDR, we screened a peptide array encompassing potential lysine methylation sites from >100 key DDR proteins and identified peptides from 58 proteins to be lysine methylated defining a methylation consensus sequence of [S>K - 2 ; S>R - 1 ; K 0 ] consistent with previous findings. We focused on K377 methylation of the Flap endonuclease 1 (FEN1), a structure specific endonuclease with important functions in Okazaki fragment processing during DNA replication as a substrate of SET7. FEN1 was monomethylated by SET7 in vivo in a cell cycle dependent manner with levels increasing as cells progressed through S phase and decreasing as they exited S phase, as detected using K377me1 specific antibodies. Although K377me1 did not affect the enzymatic activity of FEN1, it was required for the cellular response to replicative stress by FEN1. These finding define FEN1 as a new substrate of SET7 required for the DDR.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.072
Threshold uncertainty score0.504

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.014
GPT teacher head0.321
Teacher spread0.307 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations12
Published2017
Admission routes3
Has abstractyes

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