Evidence map›Paper›PMID 29983314›Full record

ArticleCurrent biology : CB2018

γ-TuRC Heterogeneity Revealed by Analysis of Mozart1.

Corinne A Tovey, Chloe E Tubman, Eva Hamrud, Zihan Zhu, Anna E Dyas, Andrew N Butterfield, Alex Fyfe, Errin Johnson, Paul T Conduit

Open access · hybridAbstract read
In one paragraph

Article in Current biology : CB, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
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  4. Mitochondrial Differentiation during Spermatogenesis: Lessons fromInternational journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. γ-Tubulin in microtubule nucleation and beyond.Frontiers in cell and developmental biology · 2022
    Review
  9. Review
  10. Article
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  14. Article
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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

9 authors at 2 institutions in 1 country.

Corinne A ToveyDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
Chloe E TubmanDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
Eva HamrudDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
Zihan ZhuDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
Anna E DyasDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
Andrew N ButterfieldDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
Alex FyfeSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Errin JohnsonSir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Paul T ConduitDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK. Electronic address: ptc29@cam.ac.uk.
University of Cambridge · GBUniversity of Oxford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Microtubules are essential for various cell processes [1] and are nucleated by multi-protein γ-tubulin ring complexes (γ-TuRCs) at various microtubule organizing centers (MTOCs), including centrosomes [2-6]. Recruitment of γ-TuRCs to different MTOCs at different times influences microtubule array formation, but how this is regulated remains an open question. It also remains unclear whether all γ-TuRCs within the same organism have the same composition and how any potential heterogeneity might influence γ-TuRC recruitment. MOZART1 (Mzt1) was recently identified as a γ-TuRC component [7, 8] and is conserved in nearly all eukaryotes [6, 9]. Mzt1 has so far been studied in cultured human cells, yeast, and plants; its absence leads to failures in γ-TuRC recruitment and cell division, resulting in cell death [7, 9-15]. Mzt1 is small (∼8.5 kDa), binds directly to core γ-TuRC components [9, 10, 14, 15], and appears to mediate the interaction between γ-TuRCs and proteins that tether γ-TuRCs to MTOCs [9, 15]. Here, we use Drosophila to investigate the function of Mzt1 in a multicellular animal for the first time. Surprisingly, we find that Drosophila Mzt1 is expressed only in the testes and is present in γ-TuRCs recruited to basal bodies, but not to mitochondria, in developing sperm cells. mzt1 mutants are viable but have defects in basal body positioning and γ-TuRC recruitment to centriole adjuncts; sperm formation is affected and mutants display a rapid age-dependent decline in sperm motility and male fertility. Our results reveal that tissue-specific and MTOC-specific γ-TuRC heterogeneity exist in Drosophila and highlight the complexity of γ-TuRC recruitment in a multicellular animal.

Indexed as

Amino Acid SequenceAnimalsBasal BodiesCell Cycle ProteinsDrosophila melanogasterDrosophila ProteinsGene Expression ProfilingMaleMicrotubule-Associated ProteinsMitochondriaSequence AlignmentSpermatozoaCell Cycle ProteinsDrosophila ProteinsMicrotubule-Associated ProteinsMzt1 protein, Drosophilacentriole adjunctcentrosomecentrosomingamma-tubulin ring complexg-TuRCmicrotubulemicrotubule organizing centerMozart1MTOCspermatogenesis

Identifiers

PMID29983314
PMCPMC6065531
OpenAlexW2852750215

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.