Evidence map›Paper›PMID 37344488›Full record

ArticleNature communications2023

Acentrosomal spindles assemble from branching microtubule nucleation near chromosomes in Xenopus laevis egg extract.

Bernardo Gouveia, Sagar U Setru, Matthew R King, Aaron Hamlin, Howard A Stone, Joshua W Shaevitz, Sabine Petry

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. The kinetochore corona orchestrates chromosome congression through transient microtubule interactions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Building on-chip cytoskeletal circuits via branched microtubule networks.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. Review
  9. Augmin is a Ran-regulated spindle assembly factor.The Journal of biological chemistry · 2023
    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

7 authors.

Bernardo Gouveia *Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ, 08544, USA.
Sagar U Setru *Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, 08544, USA.ORCID 0000-0003-1591-2291
Matthew R KingDepartment of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA.
Aaron HamlinDepartment of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA.
Howard A StoneDepartment of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ, 08544, USA.ORCID 0000-0002-9670-0639
Joshua W ShaevitzLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, 08544, USA.ORCID 0000-0001-8809-4723
Sabine PetryDepartment of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA. spetry@princeton.edu.ORCID 0000-0002-8537-9763

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Quantitavie and Computational Biology Graduate ProgramT32HG003284 · NHGRI · PRINCETON UNIVERSITY · PI Joshua Michael Akey, Stanislav Y. Shvartsman · 2004 to 2026
$9.9M
Building the Chromosome Segregation Machinery from ScratchDP2GM123493 · NIGMS · PRINCETON UNIVERSITY · PI PETRY, SABINE · 2016 to 2016
$2.4M
Role and Mechanisms of Microtubule Nucleation in Spindle AssemblyR01GM141100 · NIGMS · PRINCETON UNIVERSITY · PI PETRY, SABINE · 2022 to 2025
$2.0M
Reconstituting Early Mitotic Chromosome Movement In VitroF31CA236160 · NCI · PRINCETON UNIVERSITY · PI SETRU, SAGAR UDAYASHANKAR · 2019 to 2020
$89k
NCI NIH HHS F31 CA236160NHGRI NIH HHS T32 HG003284NIGMS NIH HHS DP2 GM123493NIGMS NIH HHS R01 GM141100NIGMS NIH HHS T32 GM007388
6 · The paper itself

Abstract

Microtubules are generated at centrosomes, chromosomes, and within spindles during cell division. Whereas microtubule nucleation at the centrosome is well characterized, much remains unknown about where, when, and how microtubules are nucleated at chromosomes. To address these questions, we reconstitute microtubule nucleation from purified chromosomes in meiotic Xenopus egg extract and find that chromosomes alone can form spindles. We visualize microtubule nucleation near chromosomes using total internal reflection fluorescence microscopy to find that this occurs through branching microtubule nucleation. By inhibiting molecular motors, we find that the organization of the resultant polar branched networks is consistent with a theoretical model where the effectors for branching nucleation are released by chromosomes, forming a concentration gradient that spatially biases branching microtbule nucleation. In the presence of motors, these branched networks are ultimately organized into functional spindles, where the number of emergent spindle poles scales with the number of chromosomes and total chromatin area.

Indexed as

MicrotubulesSpindle ApparatusAnimalsCentrosomeChromatinChromosomesXenopus laevisChromatin

Identifiers

PMID37344488
PMCPMC10284841

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.