Evidence map›Paper›PMID 24857844›Full record

ArticleMolecular & cellular proteomics : MCP2014

Using in vivo biotinylated ubiquitin to describe a mitotic exit ubiquitome from human cells.

Mingwei Min, Ugo Mayor, Gunnar Dittmar, Catherine Lindon

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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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 3 countries.

Mingwei MinFrom the ‡Department of Genetics, University of Cambridge, Downing St., Cambridge CB2 3EH, UK;
Ugo Mayor§CIC Biogune, Bizkaia Teknology Park, 48160 Derio, Basque Country, Spain; ¶Ikerbasque, Basque Foundation for Science, 48011, Bilbao, Spain;
Gunnar Dittmar‖Max Delbrück Center for Molecular Medicine, 13125 Berlin, Germany.
Catherine LindonFrom the ‡Department of Genetics, University of Cambridge, Downing St., Cambridge CB2 3EH, UK; c.lindon@gen.cam.ac.uk.
University of Cambridge · GBCIC bioGUNE · ESMax Delbrück Center · DE

Funding

Cancer Research UK C3/A10239
6 · The paper itself

Abstract

Mitotic division requires highly regulated morphological and biochemical changes to the cell. Upon commitment to exit mitosis, cells begin to remove mitotic regulators in a temporally and spatially controlled manner to bring about the changes that reestablish interphase. Ubiquitin-dependent pathways target these regulators to generate polyubiquitin-tagged substrates for degradation by the 26S proteasome. However, the lack of cell-based assays to investigate in vivo ubiquitination limits our knowledge of the identity of substrates of ubiquitin-mediated regulation in mitosis. Here we report an in vivo ubiquitin tagging system used in human cells that allows efficient purification of ubiquitin conjugates from synchronized cell populations. Coupling purification with mass spectrometry, we have identified a series of mitotic regulators targeted for polyubiquitination in mitotic exit. We show that some are new substrates of the anaphase-promoting complex/cyclosome and validate KIFC1 and RacGAP1/Cyk4 as two such targets involved respectively in timely mitotic spindle disassembly and cell spreading. We conclude that in vivo biotin tagging of ubiquitin can provide valuable information about the role of ubiquitin-mediated regulation in processes required for rebuilding interphase cells.

Indexed as

BiotinylationCell Line, TumorGTPase-Activating ProteinsHumansKinesinsMitosisProtein Interaction MappingProteomicsUbiquitinUbiquitinationGTPase-Activating ProteinsKIFC1 protein, humanKinesinsmgcRacGAPUbiquitin

Identifiers

PMID24857844
PMCPMC4159658
OpenAlexW2149203132

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.