Evidence map›Paper›PMID 10097147›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1.

A Bellacosa, L Cicchillitti, F Schepis, A Riccio, A T Yeung, Y Matsumoto, E A Golemis, M Genuardi, G Neri

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 1 pooled it
10.4field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 1 synthesis or guideline pooled it, 264 citations in OpenAlex.

  1. Meta-analysis of the association betweenThe Journal of international medical research · 2024
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Prognostic Significance ofPhenomics (Cham, Switzerland) · 2024
    Article
  8. Integrated mutational landscape analysis of poorly differentiated high-grade neuroendocrine carcinoma of the uterine cervix.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Article
  11. Base Excision DNA Repair in Plants:International journal of molecular sciences · 2023
    Review
  12. Article
  13. Article
  14. Noncatalytic Domains in DNA Glycosylases.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

46 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

A BellacosaDivisions of Population Science, Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, PA 19111, USA. A_Bellacosa@fccc.edu
L Cicchillitti
F Schepis
A Riccio
A T Yeung
Y Matsumoto
E A Golemis
M Genuardi
G Neri
Fox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
The MED1 Protein in DNA Damage Response and RepairR01CA078412 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI BELLACOSA, ALFONSO · 2004 to 2014
$3.7M
NEW HUMAN DNA REPAIR ENDONUCLEASER29CA078412 · NCI · FOX CHASE CANCER CENTER · PI BELLACOSA, ALFONSO · 1998 to 2002
$619k
NCI NIH HHS CA06927NCI NIH HHS CA78412-01NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA078412NCI NIH HHS R29 CA078412
6 · The paper itself

Abstract

The DNA mismatch repair (MMR) is a specialized system, highly conserved throughout evolution, involved in the maintenance of genomic integrity. To identify novel human genes that may function in MMR, we employed the yeast interaction trap. Using the MMR protein MLH1 as bait, we cloned MED1. The MED1 protein forms a complex with MLH1, binds to methyl-CpG-containing DNA, has homology to bacterial DNA repair glycosylases/lyases, and displays endonuclease activity. Transfection of a MED1 mutant lacking the methyl-CpG-binding domain (MBD) is associated with microsatellite instability (MSI). These findings suggest that MED1 is a novel human DNA repair protein that may be involved in MMR and, as such, may be a candidate eukaryotic homologue of the bacterial MMR endonuclease, MutH. In addition, these results suggest that cytosine methylation may play a role in human DNA repair.

Indexed as

Base Pair MismatchDNA RepairAdaptor Proteins, Signal TransducingAmino Acid SequenceBase SequenceCarrier ProteinsCell LineCloning, MolecularEndodeoxyribonucleasesHumansKineticsMicrosatellite RepeatsMolecular Sequence DataMutL Protein Homolog 1Neoplasm ProteinsNuclear ProteinsAdaptor Proteins, Signal TransducingCarrier ProteinsEndodeoxyribonucleasesMBD4 protein, humanMLH1 protein, humanMutL Protein Homolog 1Neoplasm ProteinsNuclear ProteinsOligodeoxyribonucleotidesRecombinant Fusion ProteinsRecombinant Proteins

Identifiers

PMID10097147
PMCPMC22404
OpenAlexW1992159506

What OpenQuestion holds

Texttitle and abstract
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.