Evidence map›Paper›PMID 25754639›Full record

ArticleCurrent biology : CB2015

Wash interacts with lamin and affects global nuclear organization.

Jeffrey M Verboon, Hector Rincon-Arano, Timothy R Werwie, Jeffrey J Delrow, David Scalzo, Vivek Nandakumar, Mark Groudine, Susan M Parkhurst

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 59 citations in OpenAlex.

  1. WAVE2 and REST/NRSF Regulate Clustered Gene Expression by Maintaining Heterochromatin Organization.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Article
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  4. Cells · 2025
    Review
  5. Article
  6. Article
  7. Nuclear envelope budding: Getting large macromolecular complexes out of the nucleus.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Nuclear organization and regulation of the differentiated state.Cellular and molecular life sciences : CMLS · 2021
    Review
  18. Article
  19. Article
  20. Journal of cell science · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Jeffrey M VerboonBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Hector Rincon-AranoBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Timothy R WerwieBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Jeffrey J DelrowGenomics Resource, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
David ScalzoBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Vivek NandakumarClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Mark GroudineBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Department of Radiation Oncology, University of Washington School of Medicine, Seattle, WA 98195, USA.
Susan M ParkhurstBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. Electronic address: susanp@fredhutch.org.
Fred Hutch Cancer Center · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAUniversity of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
MAINTENANCE OF GENE EXPRESSION IN THE RED CELL LINEAGER01HL065440 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GROUDINE, MARK T · 2000 to 2018
$12.4M
FUNCTION OF HUMAN &MOUSE B GLOBIN LOCUS CONTROL REGIONSR37DK044746 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GROUDINE, MARK T · 1997 to 2016
$12.3M
Chromosome Metabolism and Cancer Training GrantT32CA009657 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1991 to 2020
$7.6M
Regulation of Membrane-Cortical Cytoskeleton Crosstalk by WASHR01GM097083 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PARKHURST, SUSAN M · 2011 to 2014
$1.4M
FUNCTION OF THE HUMAN B-GLOBIN LOCUS CONTROL REGION-LCRR01DK044746 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GROUDINE, MARK T · 1992 to 1996
–
NCI NIH HHS P30 CA015704NCI NIH HHS T32 CA009657NCI NIH HHS T32CA009657NHLBI NIH HHS HL65440NHLBI NIH HHS R01 HL065440NIDDK NIH HHS DK44746NIDDK NIH HHS R37 DK044746NIGMS NIH HHS GM097083NIGMS NIH HHS R01 GM097083
6 · The paper itself

Abstract

The cytoplasmic functions of Wiskott-Aldrich syndrome family (WAS) proteins are well established and include roles in cytoskeleton reorganization and membrane-cytoskeletal interactions important for membrane/vesicle trafficking, morphogenesis, immune response, and signal transduction. Misregulation of these proteins is associated with immune deficiency and metastasis [1-4]. Cytoplasmic WAS proteins act as effectors of Rho family GTPases and polymerize branched actin through the Arp2/3 complex [1, 5]. Previously, we identified Drosophila washout (wash) as a new member of the WAS family with essential cytoplasmic roles in early development [6, 7]. Studies in mammalian cells and Dictyostelium suggest that WASH functions primarily in a multiprotein complex that regulates endosome shape and trafficking in an Arp2/3-dependent manner [8-11]. However, roles for classically cytoplasmic proteins in the nucleus are beginning to emerge, in particular, as participants in the regulation of gene expression [12, 13]. Here, we show that Drosophila Wash is present in the nucleus, where it plays a key role in global nuclear organization. wash mutant and knockdown nuclei disrupt subnuclear structures/organelles and exhibit the abnormal wrinkled morphology reminiscent of those observed in diverse laminopathies [14-16]. We find that nuclear Wash interacts with B-type Lamin (Lamin Dm0), and, like Lamin, Wash associates with constitutive heterochromatin. Wash knockdown increases chromatin accessibility of repressive compartments and results in a global redistribution of repressive histone modifications. Thus, our results reveal a novel role for Wash in modulating nucleus morphology and in the organization of both chromatin and non-chromatin nuclear sub-structures.

Indexed as

AnimalsAnimals, Genetically ModifiedCell NucleusDrosophila melanogasterDrosophila ProteinsFemaleGene Knockdown TechniquesGenes, InsectHeterochromatinLaminsMaleMutationVesicular Transport ProteinsDrosophila ProteinsHeterochromatinLaminsLam protein, DrosophilaVesicular Transport ProteinsWASH protein, Drosophila

Identifiers

PMID25754639
PMCPMC4366290
OpenAlexW2079385284

What OpenQuestion holds

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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.