Evidence map›Paper›PMID 26283374›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Screen for multi-SUMO-binding proteins reveals a multi-SIM-binding mechanism for recruitment of the transcriptional regulator ZMYM2 to chromatin.

Elisa Aguilar-Martinez, Xi Chen, Aaron Webber, A Paul Mould, Anne Seifert, Ronald T Hay, Andrew D Sharrocks

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. 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
2.4field-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

29 citing papers in PubMed, 62 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

7 authors at 2 institutions in 1 country.

Elisa Aguilar-MartinezFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom;
Xi ChenFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom;
Aaron WebberFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom;
A Paul MouldFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom;
Anne SeifertCentre for Gene Regulation and Expression, University of Dundee, Dundee DD1 5EH, United Kingdom.
Ronald T HayCentre for Gene Regulation and Expression, University of Dundee, Dundee DD1 5EH, United Kingdom.
Andrew D SharrocksFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom; a.d.sharrocks@manchester.ac.uk.
University of Manchester · GBUniversity of Dundee · GB

Funding

Medical Research Council G0701194Wellcome Trust 097945Wellcome Trust 098391Wellcome Trust 098391/Z/12/Z
6 · The paper itself

Abstract

Protein SUMOylation has emerged as an important regulatory event, particularly in nuclear processes such as transcriptional control and DNA repair. In this context, small ubiquitin-like modifier (SUMO) often provides a binding platform for the recruitment of proteins via their SUMO-interacting motifs (SIMs). Recent discoveries point to an important role for multivalent SUMO binding through multiple SIMs in the binding partner as exemplified by poly-SUMOylation acting as a binding platform for ubiquitin E3 ligases such as ring finger protein 4. Here, we have investigated whether other types of protein are recruited through multivalent SUMO interactions. We have identified dozens of proteins that bind to multi-SUMO platforms, thereby uncovering a complex potential regulatory network. Multi-SUMO binding is mediated through multi-SIM modules, and the functional importance of these interactions is demonstrated for the transcriptional corepressor ZMYM2/ZNF198 where its multi-SUMO-binding activity is required for its recruitment to chromatin.

Indexed as

ChromatinDNA-Binding ProteinsHEK293 CellsHumansProtein BindingSmall Ubiquitin-Related Modifier ProteinsTranscription FactorsChromatinDNA-Binding ProteinsSmall Ubiquitin-Related Modifier ProteinsTranscription FactorsZMYM2 protein, humanchromatinSIMSUMOZMYM2ZNF198

Identifiers

PMID26283374
PMCPMC4568223
OpenAlexW1923637409

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.