Evidence map›Paper›PMID 18463166›Full record

ArticleMolecular biology of the cell2008

A multicomponent assembly pathway contributes to the formation of acentrosomal microtubule arrays in interphase Drosophila cells.

Gregory C Rogers, Nasser M Rusan, Mark Peifer, Stephen L Rogers

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

92 citing papers in PubMed, 139 citations in OpenAlex.

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  10. The E3 ligase Poe promotes Pericentrin degradation.Molecular biology of the cell · 2023
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  13. Review
  14. TheMolecular biology of the cell · 2022
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  15. Effects of mutant lamins on nucleo-cytoskeletal coupling inFrontiers in cell and developmental biology · 2022
    Article
  16. Article
  17. Centrosome instability: when good centrosomes go bad.Cellular and molecular life sciences : CMLS · 2021
    Review
  18. Article
  19. Article
  20. Article

32 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 2 institutions in 2 countries.

Gregory C RogersDepartment of Biology, Lineberger Comprehensive Cancer Center, and Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Nasser M Rusan
Mark Peifer
Stephen L Rogers
Segeberger Kliniken · DEUniversity of North Carolina at Chapel Hill · US

Funding

A model system to study the tumor suppressor APCR01GM067236 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEIFER, MARK A. · 2002 to 2015
$2.8M
NIGMS NIH HHS R01 GM067236NIGMS NIH HHS R01GM67236
6 · The paper itself

Abstract

In animal cells, centrosomes nucleate microtubules that form polarized arrays to organize the cytoplasm. Drosophila presents an interesting paradox however, as centrosome-deficient mutant animals develop into viable adults. To understand this discrepancy, we analyzed behaviors of centrosomes and microtubules in Drosophila cells, in culture and in vivo, using a combination of live-cell imaging, electron microscopy, and RNAi. The canonical model of the cycle of centrosome function in animal cells states that centrosomes act as microtubule-organizing centers throughout the cell cycle. Unexpectedly, we found that many Drosophila cell-types display an altered cycle, in which functional centrosomes are only present during cell division. On mitotic exit, centrosomes disassemble producing interphase cells containing centrioles that lack microtubule-nucleating activity. Furthermore, steady-state interphase microtubule levels are not changed by codepleting both gamma-tubulins. However, gamma-tubulin RNAi delays microtubule regrowth after depolymerization, suggesting that it may function partially redundantly with another pathway. Therefore, we examined additional microtubule nucleating factors and found that Mini-spindles, CLIP-190, EB1, or dynein RNAi also delayed microtubule regrowth; surprisingly, this was not further prolonged when we codepleted gamma-tubulins. Taken together, these results modify our view of the cycle of centrosome function and reveal a multi-component acentrosomal microtubule assembly pathway to establish interphase microtubule arrays in Drosophila.

Indexed as

Gene Expression RegulationAnimalsCentriolesCentrosomeDrosophila melanogasterDyneinsGreen Fluorescent ProteinsInterphaseMicroscopy, Electron, TransmissionMicroscopy, FluorescenceMitosisModels, BiologicalRNA InterferenceSpindle ApparatusTubulinDyneinsGreen Fluorescent ProteinsTubulin

Identifiers

PMID18463166
PMCPMC2441692
OpenAlexW2168614708

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.