Evidence map›Paper›PMID 24077307›Full record

ArticleGenetics2013

Regulation of Toll signaling and inflammation by β-arrestin and the SUMO protease Ulp1.

Saima G Anjum, Wenjian Xu, Niusha Nikkholgh, Sukanya Basu, Yingchao Nie, Mary Thomas, Mridula Satyamurti, Bogdan A Budnik, Y Tony Ip, Alexey Veraksa

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Mutations ofInternational journal of molecular sciences · 2022
    Article
  5. Article
  6. International journal of molecular sciences · 2021
    Article
  7. Article
  8. The role of SUMOylation during development.Biochemical Society transactions · 2020
    Review
  9. Article
  10. Frontiers in cellular and infection microbiology · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. The immune signaling pathways of Manduca sexta.Insect biochemistry and molecular biology · 2015
    Article
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

10 authors at 3 institutions in 1 country.

Saima G AnjumDepartment of Biology, University of Massachusetts Boston, Boston, Massachusetts 02125.
Wenjian Xu
Niusha Nikkholgh
Sukanya Basu
Yingchao Nie
Mary Thomas
Mridula Satyamurti
Bogdan A Budnik
Y Tony Ip
Alexey Veraksa
University of Massachusetts Boston · USUniversity of Massachusetts Chan Medical School · USHarvard University · US

Funding

UMass Boston-DF/HCC U54 Partnership (2 of 2)U54CA156734 · NCI · UNIVERSITY OF MASSACHUSETTS BOSTON · PI ADAN COLON-CARMONA, Jill A. Macoska · 2010 to 2026
$24.9M
PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
University of Massachusetts Center for Clinical and Translational ScienceUL1TR000161 · NCATS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2012 to 2015
$11.0M
Genetic analysis of damage-induced intestinal stem cell division in DrosophilaR01DK083450 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI IP, Y. TONY · 2010 to 2024
$4.7M
Regulation of developmental signaling by beta-arrestinR15GM097727 · NIGMS · UNIVERSITY OF MASSACHUSETTS BOSTON · PI VERAKSA, ALEXEY · 2011 to 2011
$290k
NCATS NIH HHS UL1 TR000161NCATS NIH HHS UL1TR000161NCI NIH HHS CA156734NCI NIH HHS U54 CA156734NIDDK NIH HHS DK32520NIDDK NIH HHS DK83450NIDDK NIH HHS P30 DK032520NIDDK NIH HHS R01 DK083450NIGMS NIH HHS GM097727NIGMS NIH HHS R15 GM097727
6 · The paper itself

Abstract

The Toll signaling pathway has a highly conserved function in innate immunity and is regulated by multiple factors that fine tune its activity. One such factor is β-arrestin Kurtz (Krz), which we previously implicated in the inhibition of developmental Toll signaling in the Drosophila melanogaster embryo. Another level of controlling Toll activity and immune system homeostasis is by protein sumoylation. In this study, we have uncovered a link between these two modes of regulation and show that Krz affects sumoylation via a conserved protein interaction with a SUMO protease, Ulp1. Loss of function of krz or Ulp1 in Drosophila larvae results in a similar inflammatory phenotype, which is manifested as increased lamellocyte production; melanotic mass formation; nuclear accumulation of Toll pathway transcriptional effectors, Dorsal and Dif; and expression of immunity genes, such as Drosomycin. Moreover, mutations in krz and Ulp1 show dosage-sensitive synergistic genetic interactions, suggesting that these two proteins are involved in the same pathway. Using Dorsal sumoylation as a readout, we found that altering Krz levels can affect the efficiency of SUMO deconjugation mediated by Ulp1. Our results demonstrate that β-arrestin controls Toll signaling and systemic inflammation at the level of sumoylation.

Indexed as

Signal TransductionAnimalsArrestinsCell LineCysteine EndopeptidasesDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsInflammationNuclear ProteinsPhosphoproteinsProtein BindingSumoylationToll-Like ReceptorsTranscription FactorsArrestinsCysteine EndopeptidasesDif protein, Drosophiladl protein, DrosophilaDNA-Binding ProteinsDrosophila Proteinskrz protein, DrosophilaNuclear ProteinsPhosphoproteinsToll-Like ReceptorsTranscription FactorsUlp1 proteasearrestininflammationsumoylationTollUlp1

Identifiers

PMID24077307
PMCPMC3832275
OpenAlexW2076323985

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.