Evidence map›Paper›PMID 34014923›Full record

ArticlePLoS genetics2021

A degron-based strategy reveals new insights into Aurora B function in C. elegans.

Nikita S Divekar, Amanda C Davis-Roca, Liangyu Zhang, Abby F Dernburg, Sarah M Wignall

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  8. Temporal Analysis of DSB Repair Outcome in Caenorhabditis elegans Meiosis.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Signalling mechanisms and cellular functions of SUMO.Nature reviews. Molecular cell biology · 2022
    Review
  14. Article
  15. Article
  16. 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

5 authors at 2 institutions in 1 country.

Nikita S DivekarDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, United States of America.
Amanda C Davis-RocaDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, United States of America.ORCID 0000-0003-2656-5758
Liangyu ZhangDepartment of Molecular and Cell Biology, University of California, Berkeley, California, United States of America.ORCID 0000-0002-2701-0773
Abby F DernburgDepartment of Molecular and Cell Biology, University of California, Berkeley, California, United States of America.ORCID 0000-0001-8037-1079
Sarah M WignallDepartment of Molecular Biosciences, Northwestern University, Evanston, Illinois, United States of America.ORCID 0000-0001-9828-9356
Northwestern University · USUniversity of California, Berkeley · US

Funding

Crossover control during meiosisR01GM065591 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DERNBURG, ABBY F · 2002 to 2021
$4.5M
Molecular Biophysics Training Program at Northwestern UniversityT32GM008382 · NIGMS · NORTHWESTERN UNIVERSITY · PI RADHAKRISHNAN, ISHWAR · 1990 to 2020
$4.3M
Regulation of chromosome segregation during oocyte meiosisR01GM124354 · NIGMS · NORTHWESTERN UNIVERSITY · PI SARAH Marie WIGNALL · 2018 to 2026
$2.8M
NIGMS NIH HHS R01 GM065591NIGMS NIH HHS R01 GM124354NIGMS NIH HHS T32 GM008382
6 · The paper itself

Abstract

The widely conserved kinase Aurora B regulates important events during cell division. Surprisingly, recent work has uncovered a few functions of Aurora-family kinases that do not require kinase activity. Thus, understanding this important class of cell cycle regulators will require strategies to distinguish kinase-dependent from independent functions. Here, we address this need in C. elegans by combining germline-specific, auxin-induced Aurora B (AIR-2) degradation with the transgenic expression of kinase-inactive AIR-2. Through this approach, we find that kinase activity is essential for AIR-2's major meiotic functions and also for mitotic chromosome segregation. Moreover, our analysis revealed insight into the assembly of the ring complex (RC), a structure that is essential for chromosome congression in C. elegans oocytes. AIR-2 localizes to chromosomes and recruits other components to form the RC. However, we found that while kinase-dead AIR-2 could load onto chromosomes, other components were not recruited. This failure in RC assembly appeared to be due to a loss of RC SUMOylation, suggesting that there is crosstalk between SUMOylation and phosphorylation in building the RC and implicating AIR-2 in regulating the SUMO pathway in oocytes. Similar conditional depletion approaches may reveal new insights into other cell cycle regulators.

Indexed as

Chromosome SegregationAnimalsAurora Kinase BCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosomesMeiosisMitosisOocytesPhosphorylationReproducibility of ResultsSpindle ApparatusSumoylationair-2 protein, C elegansAurora Kinase BCaenorhabditis elegans Proteins

Identifiers

PMID34014923
PMCPMC8172070
OpenAlexW3162324946

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.