Evidence map›Paper›PMID 9689074›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

The disassembly and reassembly of functional centrosomes in vitro.

B J Schnackenberg, A Khodjakov, C L Rieder, R E Palazzo

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

68 citing papers in PubMed, 183 citations in OpenAlex.

  1. Article
  2. Article
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  6. Article
  7. Native molecular architectures of centrosomes inbioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Human centrosome organization and function in interphase and mitosis.Seminars in cell & developmental biology · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Centrosome function and assembly in animal cells.Nature reviews. Molecular cell biology · 2015
    Review
  19. Article
  20. Article

8 more citing papers are in PubMed but not listed here.

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.

B J SchnackenbergDepartment of Biochemistry, Cell, and Molecular Biology, University of Kansas, Lawrence, KS 66045, USA.
A Khodjakov
C L Rieder
R E Palazzo
University of Kansas · USMarine Biological Laboratory · USNew York State Department of Health · US

Funding

ZERNIKE PHASE-CONTRAST IMAGINGP41RR001219 · NCRR · WADSWORTH CENTER · PI WAGENKNECHT, TERENCE C · 1985 to 2010
$11.1M
FORMATION, INTERACTION, &FUNCTION OF SPINDLE COMPONENTSR01GM040198 · NIGMS · WADSWORTH CENTER · PI RIEDER, CONLY L. · 1988 to 2000
$206k
NCRR NIH HHS P41 RR001219NCRR NIH HHS P41 RR01219NIGMS NIH HHS R01 GM040198PHS HHS 40198PHS HHS 43264
6 · The paper itself

Abstract

Animal cells contain a single centrosome that nucleates and organizes a polarized array of microtubules which functions in many cellular processes. In most cells the centrosome is composed of two centrioles surrounded by an ill-defined "cloud" of pericentriolar material. Recently, gamma-tubulin-containing 25-nm diameter ring structures have been identified as likely microtubule nucleation sites within the pericentriolar material of isolated centrosomes. Here we demonstrate that when Spisula centrosomes are extracted with 1.0 M KI they lose their microtubule nucleation potential and appear by three-dimensional electron microscopy as a complex lattice, built from 12- to 15-nm thick elementary fiber(s), that lack centrioles and 25-nm rings. Importantly, when these remnants are incubated in extracts prepared from Spisula oocytes they recover their 25-nm rings, gamma-tubulin, and microtubule nucleation potential. This recovery process occurs in the absence of microtubules, divalent cations, and nucleotides. Thus, in animals the centrosome is structurally organized around a KI-insoluble filament-based "centromatrix" that serves as a scaffold to which those proteins required for microtubule nucleation bind, either directly or indirectly, in a divalent cation and nucleotide independent manner.

Indexed as

CentrosomeAmino Acid SequenceAnimalsBivalviaMicrotubule ProteinsMolecular Sequence DataOocytesMicrotubule Proteins

Identifiers

PMID9689074
PMCPMC21332
OpenAlexW2056627868

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.