Evidence map›Paper›PMID 23938469›Full record

ArticleMolecular & cellular proteomics : MCP2013

Regulation of stress-inducible phosphoprotein 1 nuclear retention by protein inhibitor of activated STAT PIAS1.

Iaci N Soares, Fabiana A Caetano, Jordan Pinder, Bruna Roz Rodrigues, Flavio H Beraldo, Valeriy G Ostapchenko, Chantal Durette, Grace Schenatto Pereira, Marilene H Lopes, Nicolle Queiroz-Hazarbassanov and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-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

16 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Heat Shock Proteins in Glioblastoma Biology: Where Do We Stand?International journal of molecular sciences · 2019
    Review
  8. SUMOylation in Glioblastoma: A Novel Therapeutic Target.International journal of molecular sciences · 2019
    Review
  9. Article
  10. Article
  11. Review
  12. Cholinergic Regulation of hnRNPA2/B1 Translation by M1 Muscarinic Receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  13. Article
  14. Article
  15. Article
  16. Review
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

20 authors at 7 institutions in 2 countries.

Iaci N SoaresRobarts Research Institute, The University of Western Ontario, London, ON, Canada;
Fabiana A Caetano
Jordan Pinder
Bruna Roz Rodrigues
Flavio H Beraldo
Valeriy G Ostapchenko
Chantal Durette
Grace Schenatto Pereira
Marilene H Lopes
Nicolle Queiroz-Hazarbassanov
Isabela W Cunha
Paulo I Sanematsu
Sergio Suzuki
Luiz F Bleggi-Torres
Caroline Schild-Poulter
Pierre Thibault
Graham Dellaire
Vilma R Martins
Vania F Prado
Marco A M Prado
National Council for Scientific and Technological Development · BRUniversidade Federal de Minas Gerais · BRWestern University · CAAC Camargo Hospital · BRDalhousie University · CAInstitute for Research in Immunology and Cancer · CAPontifícia Universidade Católica do Paraná · BR

Funding

Canadian Institutes of Health Research MOP-84260Canadian Institutes of Health Research MOP 93651
6 · The paper itself

Abstract

Stress-inducible phosphoprotein 1 (STI1), a cochaperone for Hsp90, has been shown to regulate multiple pathways in astrocytes, but its contributions to cellular stress responses are not fully understood. We show that in response to irradiation-mediated DNA damage stress STI1 accumulates in the nucleus of astrocytes. Also, STI1 haploinsufficiency decreases astrocyte survival after irradiation. Using yeast two-hybrid screenings we identified several nuclear proteins as STI1 interactors. Overexpression of one of these interactors, PIAS1, seems to be specifically involved in STI1 nuclear retention and in directing STI1 and Hsp90 to specific sub-nuclear regions. PIAS1 and STI1 co-immunoprecipitate and PIAS1 can function as an E3 SUMO ligase for STI. Using mass spectrometry we identified five SUMOylation sites in STI1. A STI1 mutant lacking these five sites is not SUMOylated, but still accumulates in the nucleus in response to increased expression of PIAS1, suggesting the possibility that a direct interaction with PIAS1 could be responsible for STI1 nuclear retention. To test this possibility, we mapped the interaction sites between PIAS1 and STI1 using yeast-two hybrid assays and surface plasmon resonance and found that a large domain in the N-terminal region of STI1 interacts with high affinity with amino acids 450-480 of PIAS1. Knockdown of PIAS1 in astrocytes impairs the accumulation of nuclear STI1 in response to irradiation. Moreover, a PIAS1 mutant lacking the STI1 binding site is unable to increase STI1 nuclear retention. Interestingly, in human glioblastoma multiforme PIAS1 expression is increased and we found a significant correlation between increased PIAS1 expression and STI1 nuclear localization. These experiments provide evidence that direct interaction between STI1 and PIAS1 is involved in the accumulation of nuclear STI1. This retention mechanism could facilitate nuclear chaperone activity.

Indexed as

AnimalsAstrocytesCell DeathCell NucleusCells, CulturedDNA DamageGamma RaysGene Knockdown TechniquesHaploinsufficiencyHeat-Shock ProteinsHEK293 CellsHumansMiceMice, Inbred C57BLMice, KnockoutProtein Inhibitors of Activated STATHeat-Shock ProteinsPias1 protein, mouseProtein Inhibitors of Activated STATRecombinant Fusion ProteinsStip1 protein, mouse

Identifiers

PMID23938469
PMCPMC3820937
OpenAlexW2128151927

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.