Evidence map›Paper›PMID 12960380›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Nuclear actin and protein 4.1: essential interactions during nuclear assembly in vitro.

Sharon Wald Krauss, Cynthia Chen, Sheldon Penman, Rebecca Heald

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed, 101 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. The Role of Emerin in Cancer Progression and Metastasis.International journal of molecular sciences · 2021
    Review
  5. Review
  6. Review
  7. Article
  8. Multiple Pools of Nuclear Actin.Anatomical record (Hoboken, N.J. : 2007) · 2018
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Diseases of the Nucleoskeleton.Comprehensive Physiology · 2016
    Review
  17. Review
  18. Article
  19. Nuclear actin and myosins in adenovirus infection.Experimental cell research · 2015
    Article
  20. 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

4 authors at 3 institutions in 1 country.

Sharon Wald KraussDepartment of Subcellular Structure, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720, USA. sakrauss@lbl.gov
Cynthia Chen
Sheldon Penman
Rebecca Heald
University of California, Berkeley · USLawrence Berkeley National Laboratory · USMassachusetts Institute of Technology · US

Funding

STUDYING SPINDLE ASSEMBLY AND FUNCTION USING DNA BEADSR01GM057839 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HEALD, REBECCA W · 1998 to 2014
$3.3M
RED CELL CYTOSKELETAL PROTEIN 4.1 DURING CELL DIVISIONR01DK059079 · NIDDK · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI KRAUSS, SHARON W · 2000 to 2008
$2.0M
NIDDK NIH HHS DK59079NIDDK NIH HHS R01 DK059079NIGMS NIH HHS GM57839NIGMS NIH HHS R01 GM057839
6 · The paper itself

Abstract

Structural protein 4.1, which has crucial interactions within the spectrin-actin lattice of the human red cell membrane skeleton, also is widely distributed at diverse intracellular sites in nucleated cells. We previously showed that 4.1 is essential for assembly of functional nuclei in vitro and that the capacity of 4.1 to bind actin is required. Here we report that 4.1 and actin colocalize in mammalian cell nuclei using fluorescence microscopy and, by higher-resolution detergent-extracted cell whole-mount electron microscopy, are associated on nuclear filaments. We also devised a cell-free assay using Xenopus egg extract containing fluorescent actin to follow actin during nuclear assembly. By directly imaging actin under nonperturbing conditions, the total nuclear actin population is retained and visualized in situ relative to intact chromatin. We detected actin initially when chromatin and nuclear pores began assembling. As nuclear lamina assembled, but preceding DNA synthesis, actin distributed in a reticulated pattern throughout the nucleus. Protein 4.1 epitopes also were detected when actin began to accumulate in nuclei, producing a diffuse coincident pattern. As nuclei matured, actin was detected both coincident with and also independent of 4.1 epitopes. To test whether acquisition of nuclear actin is required for nuclear assembly, the actin inhibitor latrunculin A was added to Xenopus egg extracts during nuclear assembly. Latrunculin A strongly perturbed nuclear assembly and produced distorted nuclear structures containing neither actin nor protein 4.1. Our results suggest that actin as well as 4.1 is necessary for nuclear assembly and that 4.1-actin interactions may be critical.

Indexed as

Cytoskeletal ProteinsNeuropeptidesActinsAnimalsCell LineCell NucleusDNA ReplicationHumansMembrane ProteinsMicroscopy, FluorescenceMicroscopy, ImmunoelectronProtein BindingXenopusActinsCytoskeletal Proteinserythrocyte membrane band 4.1 proteinerythrocyte membrane protein band 4.1-like 1Membrane ProteinsNeuropeptides

Identifiers

PMID12960380
PMCPMC196875
OpenAlexW2128889123

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.