Evidence map›Paper›PMID 17938197›Full record

ArticleMolecular and cellular biology2007

UBE2T, the Fanconi anemia core complex, and FANCD2 are recruited independently to chromatin: a basis for the regulation of FANCD2 monoubiquitination.

Arno Alpi, Frederic Langevin, Georgina Mosedale, Yuichi J Machida, Anindya Dutta, Ketan J Patel

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. The role of ubiquitin-conjugating enzyme in the process of spermatogenesis.Reproductive biology and endocrinology : RB&E · 2024
    Review
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Arno AlpiLaboratory of Molecular Biology, Medical Research Council, Cambridge, United Kingdom.
Frederic Langevin
Georgina Mosedale
Yuichi J Machida
Anindya Dutta
Ketan J Patel
Medical Research Council · GBMRC Laboratory of Molecular Biology · GBUniversity of Virginia · US

Funding

Medical Research Council MC_U105178811
6 · The paper itself

Abstract

The Fanconi anemia (FA) nuclear core complex and the E2 ubiquitin-conjugating enzyme UBE2T are required for the S phase and DNA damage-restricted monoubiquitination of FANCD2. This constitutes a key step in the FA tumor suppressor pathway, and much attention has been focused on the regulation at this point. Here, we address the importance of the assembly of the FA core complex and the subcellular localization of UBE2T in the regulation of FANCD2 monoubiquitination. We establish three points. First, the stable assembly of the FA core complex can be dissociated of its ability to function as an E3 ubiquitin ligase. Second, the actual E3 ligase activity is not determined by the assembly of the FA core complex but rather by its DNA damage-induced localization to chromatin. Finally, UBE2T and FANCD2 access this subcellular fraction independently of the FA core complex. FANCD2 monoubiquitination is therefore not regulated by multiprotein complex assembly but by the formation of an active E2/E3 holoenzyme on chromatin.

Indexed as

UbiquitinationAnimalsCatalytic DomainCell CycleCell LineChickensChromatinDNA DamageFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group L ProteinHumansProtein BindingUbiquitin-Conjugating EnzymesChromatinFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group L ProteinUbiquitin-Conjugating Enzymes

Identifiers

PMID17938197
PMCPMC2169426
OpenAlexW2145079065

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.