Evidence map›Paper›PMID 10713167›Full record

ArticleMolecular and cellular biology2000

Nucleotide excision repair/TFIIH helicases RAD3 and SSL2 inhibit short-sequence recombination and Ty1 retrotransposition by similar mechanisms.

B S Lee, L Bi, D J Garfinkel, A M Bailis

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. 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
1.7field-weighted citation impact, top 16% 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, 45 citations in OpenAlex.

  1. Article
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  9. Retrotransposition is associated with genome instability during chronological aging.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
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  13. Review
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  15. Review
  16. Article
  17. The DNA repair genes XPB and XPD defend cells from retroviral infection.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  18. Article
  19. Article
  20. Activation of a LTR-retrotransposon by telomere erosion.Proceedings of the National Academy of Sciences of the United States of America · 2003
    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 3 institutions in 1 country.

B S LeeGene Regulation and Chromosome Biology Laboratory, National Cancer Institute-Frederick Cancer Research and Development Center, National Institutes of Health, Frederick, Maryland 21702-1201, USA.
L Bi
D J Garfinkel
A M Bailis
City Of Hope National Medical Center · USFrederick National Laboratory for Cancer Research · USNational Institutes of Health · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Ty Element Retrotransposition in S. cerevisiaeZ01BC010340 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GARFINKEL, DAVID J. · 2000 to 2008
$2.6M
GENOME STABILITY IN RAD MUTANTSR01GM057484 · NIGMS · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI BAILIS, ADAM M · 1998 to 2006
$2.0M
NCI NIH HHS CA33572NCI NIH HHS P30 CA033572NIGMS NIH HHS GM57484NIGMS NIH HHS R01 GM057484
6 · The paper itself

Abstract

Eukaryotic genomes contain potentially unstable sequences whose rearrangement threatens genome structure and function. Here we show that certain mutant alleles of the nucleotide excision repair (NER)/TFIIH helicase genes RAD3 and SSL2 (RAD25) confer synthetic lethality and destabilize the Saccharomyces cerevisiae genome by increasing both short-sequence recombination and Ty1 retrotransposition. The rad3-G595R and ssl2-rtt mutations do not markedly alter Ty1 RNA or protein levels or target site specificity. However, these mutations cause an increase in the physical stability of broken DNA molecules and unincorporated Ty1 cDNA, which leads to higher levels of short-sequence recombination and Ty1 retrotransposition. Our results link components of the core NER/TFIIH complex with genome stability, homologous recombination, and host defense against Ty1 retrotransposition via a mechanism that involves DNA degradation.

Indexed as

Recombination, GeneticSaccharomyces cerevisiae ProteinsTATA-Binding Protein Associated FactorsTranscription Factors, TFIITranscription Factor TFIIDAdenosine TriphosphatasesDeoxyribonucleases, Type II Site-SpecificDNADNA HelicasesDNA RepairFungal ProteinsGenes, FungalMutagenesis, InsertionalMutationPlasmidsRetroelementsAdenosine TriphosphatasesDeoxyribonucleases, Type II Site-SpecificDNADNA HelicasesFungal ProteinsRad3 protein, S cerevisiaeRetroelementsSaccharomyces cerevisiae ProteinsSCEI protein, S cerevisiaeSSL2 protein, S cerevisiaeTAF6 protein, S cerevisiaeTATA-Binding Protein Associated FactorsTranscription FactorsTranscription Factors, TFIITranscription Factor TFIIDTranscription Factor TFIIH

Identifiers

PMID10713167
PMCPMC85430
OpenAlexW2114405122

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.